Welcome to LookChem.com Sign In|Join Free

CAS

  • or

52488-36-5

Post Buying Request

52488-36-5 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

52488-36-5 Usage

Chemical Properties

Clear yellowish-green or dark brown liquid

Uses

Different sources of media describe the Uses of 52488-36-5 differently. You can refer to the following data:
1. 4-Bromoindole is a potential inhibitor of GSK-3. It is also used as pharmaceutical intermediates.
2. 4-Bromoindole may be used to synthesize:clavicipitic acid, an ergot alkaloid4-bromodehydrotryptophan3-indolylacetonitrile derivativemarine alkaloid dictyodendrin B

Check Digit Verification of cas no

The CAS Registry Mumber 52488-36-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,4,8 and 8 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 52488-36:
(7*5)+(6*2)+(5*4)+(4*8)+(3*8)+(2*3)+(1*6)=135
135 % 10 = 5
So 52488-36-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H5BrN2/c8-6-4-10-7-5(6)2-1-3-9-7/h1-4H,(H,9,10)

52488-36-5 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (L19417)  4-Bromoindole, 98%   

  • 52488-36-5

  • 250mg

  • 224.0CNY

  • Detail
  • Alfa Aesar

  • (L19417)  4-Bromoindole, 98%   

  • 52488-36-5

  • 1g

  • 564.0CNY

  • Detail
  • Alfa Aesar

  • (L19417)  4-Bromoindole, 98%   

  • 52488-36-5

  • 5g

  • 1883.0CNY

  • Detail
  • Aldrich

  • (524336)  4-Bromoindole  96%

  • 52488-36-5

  • 524336-1ML

  • 1,014.39CNY

  • Detail
  • Aldrich

  • (524336)  4-Bromoindole  96%

  • 52488-36-5

  • 524336-5ML

  • 3,608.28CNY

  • Detail

52488-36-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-bromo-1H-indole

1.2 Other means of identification

Product number -
Other names 4-Brom-indol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:52488-36-5 SDS

52488-36-5Synthetic route

4-bromo-1-[(4-methylphenyl)sulfonyl]-1H-indole
90481-72-4

4-bromo-1-[(4-methylphenyl)sulfonyl]-1H-indole

4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

Conditions
ConditionsYield
With sodium hydroxide In methanol for 12h; Heating;98%
4-bromo-1-(trifluoromethylsulfonyl)indole
1180007-97-9

4-bromo-1-(trifluoromethylsulfonyl)indole

4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

Conditions
ConditionsYield
With sodium hydroxide In methanol; water at 100℃; for 12h;96%
4-bromo-2,3-dihydro-1H-indole
86626-38-2

4-bromo-2,3-dihydro-1H-indole

4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

Conditions
ConditionsYield
With sodium carbonate In ethyl acetate at 120℃; for 24h; Sealed tube; Green chemistry;95%
With TEMPOL; oxygen; copper(l) chloride at 50 - 60℃; for 4.5h; Inert atmosphere;95%
With oxygen; sodium t-butanolate In dimethyl sulfoxide at 60℃; under 760.051 Torr; for 4h;48%
1-(4-bromo-1H-indol-1-yl)-2,2-dimethylpropan-1-one
1196981-04-0

1-(4-bromo-1H-indol-1-yl)-2,2-dimethylpropan-1-one

4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

Conditions
ConditionsYield
With water; 1,8-diazabicyclo[5.4.0]undec-7-ene In tetrahydrofuran for 3h; Reflux;94%
4-bromo-1-methoxycarbonylindole
101909-45-9

4-bromo-1-methoxycarbonylindole

4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

Conditions
ConditionsYield
With sodium hydroxide In methanol for 1h; Heating;88.5%
1-bromo-2-ethenyl-3-nitrobenzene
90481-68-8

1-bromo-2-ethenyl-3-nitrobenzene

4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

Conditions
ConditionsYield
With carbon monoxide; triphenylphosphine; palladium diacetate In acetonitrile under 3040 Torr; for 15h; Heating;84%
With carbon monoxide; triphenylphosphine; palladium diacetate In acetonitrile under 3040 Torr; for 15h; Product distribution; Heating; other catalysts, phosphine, bases, solvents; palladium-catalyzed reductive heteroannulation of 2-nitrostyrenes in the presence of CO;84%
Multi-step reaction with 2 steps
1: 96.6 percent / Fe / acetic acid; ethanol / 5 h / Heating
2: 46.3 percent / p-benzoquinone, LiCl, PdCl2(CH3CN)2 / tetrahydrofuran / 22 h / 100 °C / sealed tube
View Scheme
Multi-step reaction with 4 steps
1: 96.6 percent / Fe / acetic acid; ethanol / 5 h / Heating
2: pyridine / 0.33 h / Heating
3: 76.7 percent / p-benzoquinone, LiCl, PdCl2(CH3CN)2 / tetrahydrofuran / 18 h / Heating
4: 98 percent / 20percent aq. NaOH / methanol / 12 h / Heating
View Scheme
methanol
67-56-1

methanol

carbon monoxide
201230-82-2

carbon monoxide

1-bromo-2-ethenyl-3-nitrobenzene
90481-68-8

1-bromo-2-ethenyl-3-nitrobenzene

A

4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

B

methyl (3-bromo-2-vinylphenyl)carbamate

methyl (3-bromo-2-vinylphenyl)carbamate

Conditions
ConditionsYield
With 1,3-bis-(diphenylphosphino)propane; palladium diacetate In N,N-dimethyl-formamide under 3040 Torr; for 22h; Heating;A 76%
B 17%
N-(3-bromo-2-(2-(trimethylsilyl)ethynyl)phenyl)-2-hydroxy-2-methylpropanamide
1244651-69-1

N-(3-bromo-2-(2-(trimethylsilyl)ethynyl)phenyl)-2-hydroxy-2-methylpropanamide

4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

Conditions
ConditionsYield
With sodium hydroxide In N,N-dimethyl-formamide at 140℃; for 56h; Inert atmosphere;75%
With sodium hydroxide In N,N-dimethyl-formamide at 140℃; for 5h; Inert atmosphere;75%
1H-indol-4-yl trifluoromethanesulfonate

1H-indol-4-yl trifluoromethanesulfonate

4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

Conditions
ConditionsYield
With potassium fluoride; tris-(dibenzylideneacetone)dipalladium(0); t-BuBrettPhos; potassium bromide In 1,4-dioxane at 130℃; for 16h; Inert atmosphere;74%
4-bromo-2,3-dihydro-1H-indole
86626-38-2

4-bromo-2,3-dihydro-1H-indole

nitrobenzene
98-95-3

nitrobenzene

A

4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

B

aniline
62-53-3

aniline

Conditions
ConditionsYield
With nickel-nitrogen-doped carbon framework In water at 145℃; for 18h; Inert atmosphere; Sealed tube; Green chemistry;A 70%
B 74%
2-(2-amino-6-bromophenyl)ethan-1-ol
109277-82-9

2-(2-amino-6-bromophenyl)ethan-1-ol

4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

Conditions
ConditionsYield
tris(triphenylphosphine)ruthenium(II) chloride In toluene for 6h; Heating;73%
tris(triphenylphosphine)ruthenium(II) chloride In toluene for 6h; Rate constant; Heating;73%
With C72H79O35Ru4; o-phenylenebis(diphenylphosphine); oxygen In toluene at 130℃; for 4h; Inert atmosphere;71%
[(E)-2-(2-Bromo-6-nitro-phenyl)-vinyl]-dimethyl-amine
105205-47-8

[(E)-2-(2-Bromo-6-nitro-phenyl)-vinyl]-dimethyl-amine

4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

Conditions
ConditionsYield
With zinc In acetic acid at 85℃; for 2h;70%
With acetic acid; zinc In methanol; dichloromethane Heating;67%
1-[(E)-2-(2-Bromo-6-nitro-phenyl)-vinyl]-pyrrolidine

1-[(E)-2-(2-Bromo-6-nitro-phenyl)-vinyl]-pyrrolidine

4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

Conditions
ConditionsYield
With zinc In acetic acid Reduction; cyclization;70%
4-bromo-1H-indole-3-carboxylic acid methyl ester
101909-43-7

4-bromo-1H-indole-3-carboxylic acid methyl ester

4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

Conditions
ConditionsYield
With sodium hydroxide In methanol for 1.5h; Heating;69.1%
With sodium hydroxide In methanol for 1.5h; Heating;60.5%
4-bromo-2,3-dihydro-1H-indole
86626-38-2

4-bromo-2,3-dihydro-1H-indole

4-chlorobenzonitrile
100-00-5

4-chlorobenzonitrile

A

4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

B

4-chloro-aniline
106-47-8

4-chloro-aniline

Conditions
ConditionsYield
With nickel-nitrogen-doped carbon framework In water at 145℃; for 18h; Inert atmosphere; Sealed tube; Green chemistry;A 53%
B 52%
3-bromo-2-ethenylaniline
90481-69-9

3-bromo-2-ethenylaniline

4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

Conditions
ConditionsYield
With dichloro bis(acetonitrile) palladium(II); p-benzoquinone; lithium chloride In tetrahydrofuran at 100℃; for 22h; sealed tube;46.3%
Multi-step reaction with 3 steps
1: pyridine / 0.33 h / Heating
2: 76.7 percent / p-benzoquinone, LiCl, PdCl2(CH3CN)2 / tetrahydrofuran / 18 h / Heating
3: 98 percent / 20percent aq. NaOH / methanol / 12 h / Heating
View Scheme
4-bromo-1H-indole-2-carboxylic acid
16732-64-2

4-bromo-1H-indole-2-carboxylic acid

4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

Conditions
ConditionsYield
With quinoline; copper(I) bromide at 250℃;
(2-Bromo-6-nitro-phenyl)-acetaldehyde
85355-50-6

(2-Bromo-6-nitro-phenyl)-acetaldehyde

4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

Conditions
ConditionsYield
With sodium acetate; iron; acetic acid In ethanol; water for 2h; Heating; Yield given;
Acetic acid 2-(2-bromo-6-nitro-phenyl)-1-chloro-ethyl ester
85355-40-4

Acetic acid 2-(2-bromo-6-nitro-phenyl)-1-chloro-ethyl ester

4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

Conditions
ConditionsYield
With sodium acetate; iron; acetic acid In ethanol; water for 2h; Heating;
2-bromo-6-nitrotoluene
55289-35-5

2-bromo-6-nitrotoluene

N,N-dimethyl-formamide dimethyl acetal
4637-24-5

N,N-dimethyl-formamide dimethyl acetal

4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

Conditions
ConditionsYield
Stage #1: 2-bromo-6-nitrotoluene; N,N-dimethyl-formamide dimethyl acetal With pyrrolidine In N,N-dimethyl-formamide at 110℃; for 5h;
Stage #2: With acetic acid; zinc at 85℃; for 3h;
25.2 g
3-nitro-o-tolylamine
603-83-8

3-nitro-o-tolylamine

4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1.1: aq. HBr / 0.33 h / Heating
1.2: aq. NaNO2 / 0.25 h / 0 - 5 °C
1.3: 90 percent / CuBr; aq. HBr / 0.33 h / 100 °C
2.1: pyrrolidine / dimethylformamide / 5 h / 110 °C
2.2: 25.2 g / aq. HOAc; zinc / 3 h / 85 °C
View Scheme
Multi-step reaction with 6 steps
2: 98 percent / Br2, benzoyl peroxide / CCl4 / 14 h / Heating; Irradiation
3: CHCl3 / 0.17 h / Heating
4: 85.1 percent / Et3N / CH2Cl2 / 1 h / Ambient temperature
5: 96.6 percent / Fe / acetic acid; ethanol / 5 h / Heating
6: 46.3 percent / p-benzoquinone, LiCl, PdCl2(CH3CN)2 / tetrahydrofuran / 22 h / 100 °C / sealed tube
View Scheme
Multi-step reaction with 8 steps
2: 98 percent / Br2, benzoyl peroxide / CCl4 / 14 h / Heating; Irradiation
3: CHCl3 / 0.17 h / Heating
4: 85.1 percent / Et3N / CH2Cl2 / 1 h / Ambient temperature
5: 96.6 percent / Fe / acetic acid; ethanol / 5 h / Heating
6: pyridine / 0.33 h / Heating
7: 76.7 percent / p-benzoquinone, LiCl, PdCl2(CH3CN)2 / tetrahydrofuran / 18 h / Heating
8: 98 percent / 20percent aq. NaOH / methanol / 12 h / Heating
View Scheme
2-bromo-6-nitrotoluene
55289-35-5

2-bromo-6-nitrotoluene

4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: CuI; DMF / 0.33 h / 180 °C / 6000.6 - 7500.75 Torr / microwave irradiation
2: 67 percent / Zn; AcOH / methanol; CH2Cl2 / Heating
View Scheme
Multi-step reaction with 2 steps
1: 1.) Triton B, 2.) Zn, CaCl2 / 1.) Me2SO, 95 deg C, 1 h, 2.) H2O, reflux
2: 73 percent / RuCl2(PPh3)3 / toluene / 6 h / Heating
View Scheme
Multi-step reaction with 2 steps
1: pyrrolidine / dimethylformamide / 110 °C
2: 70 percent / Zn / acetic acid / 2 h / 85 °C
View Scheme
3-methoxycarbonylindole
942-24-5

3-methoxycarbonylindole

4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1.1: thallium(III) trifluoroacetate / trifluoroacetic acid / 2 h / 20 °C
1.2: 63 percent / CuBr2 / dimethylformamide / 1 h / 120 °C
2.1: 69.1 percent / aq. NaOH / methanol / 1.5 h / Heating
View Scheme
Multi-step reaction with 2 steps
1: 1.) TTFA, 2.) CuBr2 / 1.) TFA, room temp., 2 h; 2.) DMF, 120 deg C, 1 h
2: 60.5 percent / 40percent NaOH / methanol / 1.5 h / Heating
View Scheme
2-bromo-6-nitroaniline
59255-95-7

2-bromo-6-nitroaniline

4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: H2SO4, isoamyl nitrite / ethanol / 1 h / 0 °C
2: LiCl, HCl, CuCl*2H2O / acetone; H2O / 1.) 2 h, 3 to 10 deg C, 2.) 2 h, room temp., 3.) 2 h, room temp.
3: Fe, HOAc, sodium acetate dihydrate / ethanol; H2O / 2 h / Heating
View Scheme
Multi-step reaction with 3 steps
1: H2SO4, isoamyl nitrite / ethanol / 1 h / 0 °C
2: LiCl, HCl, CuCl*2H2O / acetone; H2O / 1.) 2 h, 3 to 10 deg C, 2.) 2 h, room temp., 3.) 2 h, room temp.
3: Fe, HOAc, sodium acetate dihydrate / ethanol; H2O / 2 h / Heating
View Scheme
2-Bromo-6-nitro-benzenediazonium; hydrogen sulfate
85355-33-5

2-Bromo-6-nitro-benzenediazonium; hydrogen sulfate

4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: LiCl, HCl, CuCl*2H2O / acetone; H2O / 1.) 2 h, 3 to 10 deg C, 2.) 2 h, room temp., 3.) 2 h, room temp.
2: Fe, HOAc, sodium acetate dihydrate / ethanol; H2O / 2 h / Heating
View Scheme
Multi-step reaction with 2 steps
1: LiCl, HCl, CuCl*2H2O / acetone; H2O / 1.) 2 h, 3 to 10 deg C, 2.) 2 h, room temp., 3.) 2 h, room temp.
2: Fe, HOAc, sodium acetate dihydrate / ethanol; H2O / 2 h / Heating
View Scheme
3-bromo-2-(bromomethyl)-1-nitrobenzene
58579-54-7

3-bromo-2-(bromomethyl)-1-nitrobenzene

4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: CHCl3 / 0.17 h / Heating
2: 85.1 percent / Et3N / CH2Cl2 / 1 h / Ambient temperature
3: 96.6 percent / Fe / acetic acid; ethanol / 5 h / Heating
4: 46.3 percent / p-benzoquinone, LiCl, PdCl2(CH3CN)2 / tetrahydrofuran / 22 h / 100 °C / sealed tube
View Scheme
Multi-step reaction with 6 steps
1: CHCl3 / 0.17 h / Heating
2: 85.1 percent / Et3N / CH2Cl2 / 1 h / Ambient temperature
3: 96.6 percent / Fe / acetic acid; ethanol / 5 h / Heating
4: pyridine / 0.33 h / Heating
5: 76.7 percent / p-benzoquinone, LiCl, PdCl2(CH3CN)2 / tetrahydrofuran / 18 h / Heating
6: 98 percent / 20percent aq. NaOH / methanol / 12 h / Heating
View Scheme
N-tosyl-3-bromo-2-ethenylaniline
90481-71-3

N-tosyl-3-bromo-2-ethenylaniline

4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 76.7 percent / p-benzoquinone, LiCl, PdCl2(CH3CN)2 / tetrahydrofuran / 18 h / Heating
2: 98 percent / 20percent aq. NaOH / methanol / 12 h / Heating
View Scheme
(2-Bromo-6-nitro-benzyl)-triphenyl-phosphonium; bromide
90481-67-7

(2-Bromo-6-nitro-benzyl)-triphenyl-phosphonium; bromide

4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 85.1 percent / Et3N / CH2Cl2 / 1 h / Ambient temperature
2: 96.6 percent / Fe / acetic acid; ethanol / 5 h / Heating
3: 46.3 percent / p-benzoquinone, LiCl, PdCl2(CH3CN)2 / tetrahydrofuran / 22 h / 100 °C / sealed tube
View Scheme
Multi-step reaction with 5 steps
1: 85.1 percent / Et3N / CH2Cl2 / 1 h / Ambient temperature
2: 96.6 percent / Fe / acetic acid; ethanol / 5 h / Heating
3: pyridine / 0.33 h / Heating
4: 76.7 percent / p-benzoquinone, LiCl, PdCl2(CH3CN)2 / tetrahydrofuran / 18 h / Heating
5: 98 percent / 20percent aq. NaOH / methanol / 12 h / Heating
View Scheme
2-(2-bromo-6-nitrophenyl)ethan-1-ol
118665-02-4

2-(2-bromo-6-nitrophenyl)ethan-1-ol

4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: Zn/CaCl2/H2O / ethanol / Heating
2: 73 percent / RuCl2(PPh3)3 / toluene / 6 h / Heating
View Scheme
4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

N,N-dimethyl-formamide
68-12-2, 33513-42-7

N,N-dimethyl-formamide

4-bromo-1H-indole-3-carbaldehyde
98600-34-1

4-bromo-1H-indole-3-carbaldehyde

Conditions
ConditionsYield
With trichlorophosphate at 20℃; for 1h; Vilsmeier-Hack formylation;100%
Stage #1: N,N-dimethyl-formamide With trichlorophosphate Cooling with ice;
Stage #2: 4-bromo-1H-indole In N,N-dimethyl-formamide at 20℃; Cooling with ice;
Stage #3: With water; potassium hydroxide In N,N-dimethyl-formamide Reflux;
100%
Stage #1: 4-bromo-1H-indole; N,N-dimethyl-formamide With trichlorophosphate at 0 - 25℃;
Stage #2: With potassium hydroxide In water Reflux;
100%
4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

bis(pinacol)diborane
73183-34-3

bis(pinacol)diborane

indole-4-boronic acid pinacol ester
388116-27-6

indole-4-boronic acid pinacol ester

Conditions
ConditionsYield
With potassium acetate; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2 In dimethyl sulfoxide at 90℃; for 4h;100%
With potassium acetate; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2 In dimethyl sulfoxide at 90℃; for 4h;100%
With tris-(dibenzylideneacetone)dipalladium(0); potassium acetate; XPhos In 1,4-dioxane at 110℃; for 20h; Miyaura borylation; Inert atmosphere;93%
4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

methyl iodide
74-88-4

methyl iodide

4-bromo-1-methyl-1H-indole
590417-55-3

4-bromo-1-methyl-1H-indole

Conditions
ConditionsYield
With sodium hydride In N,N-dimethyl-formamide at 20℃; for 3h;100%
Stage #1: 4-bromo-1H-indole With sodium hydride In tetrahydrofuran at 0℃; for 0.5h; Schlenk technique;
Stage #2: methyl iodide In tetrahydrofuran at 0 - 20℃; Schlenk technique;
100%
With sodium hydride In tetrahydrofuran at 20℃; for 4h;98%
4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

di-tert-butyl dicarbonate
24424-99-5

di-tert-butyl dicarbonate

4-bromoindole-1-carboxylic acid tert-butyl ester
676448-17-2

4-bromoindole-1-carboxylic acid tert-butyl ester

Conditions
ConditionsYield
With dmap In tetrahydrofuran for 0.25h;100%
In dichloromethane at 20℃; for 8h;99%
With dmap In dichloromethane at 20℃; for 8h; Inert atmosphere;98%
4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

2-(tert-butyldimethylsilyloxy)ethyl bromide
86864-60-0

2-(tert-butyldimethylsilyloxy)ethyl bromide

4-bromo-1-[3-(tert-butyldimethylsilyloxy)prop-1-yl]-1H-indole
603305-12-0

4-bromo-1-[3-(tert-butyldimethylsilyloxy)prop-1-yl]-1H-indole

Conditions
ConditionsYield
Stage #1: 4-bromo-1H-indole With sodium hydride In DMF (N,N-dimethyl-formamide)
Stage #2: 2-(tert-butyldimethylsilyloxy)ethyl bromide In DMF (N,N-dimethyl-formamide) at 0 - 20℃; for 1h;
100%
4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

thiophenol
108-98-5

thiophenol

4-bromo-3-(phenylthio)-1H-indole
945000-87-3

4-bromo-3-(phenylthio)-1H-indole

Conditions
ConditionsYield
With iodine; potassium iodide In ethanol; water at 45℃; for 12.0833h;99.5%
With iodine; potassium iodide In ethanol; water at 20 - 60℃;92%
4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

N-(tert-butoxycarbonyl)-α-(phenylsulfonyl)-4-bromobenzylamine
479423-30-8

N-(tert-butoxycarbonyl)-α-(phenylsulfonyl)-4-bromobenzylamine

C20H20Br2N2O2

C20H20Br2N2O2

Conditions
ConditionsYield
With potassium fluoride; C46H34I4O6 In m-xylene at 20℃; for 12h; Friedel-Crafts Alkylation; Schlenk technique; enantioselective reaction;99%
4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

tert-butyl N-(phenyl(phenylsulfonyl)methyl)carbamate
155396-71-7

tert-butyl N-(phenyl(phenylsulfonyl)methyl)carbamate

4-bromo-3-[phenyl(phenylsulfonyl)methyl]-1H-indole

4-bromo-3-[phenyl(phenylsulfonyl)methyl]-1H-indole

Conditions
ConditionsYield
With dipotassium peroxodisulfate In toluene at 20℃; for 48h; Friedel-Crafts Alkylation; Inert atmosphere; Schlenk technique; regioselective reaction;99%
4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

ethanol
64-17-5

ethanol

carbon monoxide
201230-82-2

carbon monoxide

ethyl indole-4-carboxylate
50614-84-1

ethyl indole-4-carboxylate

Conditions
ConditionsYield
With 1,1'-bis-(diphenylphosphino)ferrocene; bis(benzonitrile)palladium(II) dichloride; triethylamine at 130℃; under 18751.5 Torr; for 20h;98%
4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

1-Bromopentane
110-53-2

1-Bromopentane

4-bromo-1-pentyl-1H-indole
912568-78-6

4-bromo-1-pentyl-1H-indole

Conditions
ConditionsYield
In N,N-dimethyl-formamide; mineral oil98%
Stage #1: 4-bromo-1H-indole With sodium hydride In N,N-dimethyl-formamide at 0℃; for 0.5h;
Stage #2: 1-Bromopentane In N,N-dimethyl-formamide at 0 - 20℃; for 6h;
98%
Stage #1: 4-bromo-1H-indole With sodium hydride In N,N-dimethyl-formamide at 0℃; for 0.5h;
Stage #2: 1-Bromopentane In N,N-dimethyl-formamide at 0 - 20℃; for 6h;
98%
4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

trifluoromethane sulfonyl chloride
421-83-0

trifluoromethane sulfonyl chloride

4-bromo-3-((trifluoromethyl)thio)-1H-indole

4-bromo-3-((trifluoromethyl)thio)-1H-indole

Conditions
ConditionsYield
With 1,2,2,3,4,4-hexamethylphosphetane 1-oxide; phenylsilane In 1,4-dioxane at 40℃; Schlenk technique; Sealed tube; Inert atmosphere;98%
With trimethylphosphane In tetrahydrofuran at -78 - 20℃; for 52h; regioselective reaction;74%
4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

potassium phenyltrifluoborate

potassium phenyltrifluoborate

4-phenyl-1H-indole
35577-92-5

4-phenyl-1H-indole

Conditions
ConditionsYield
With palladium diacetate; sodium carbonate In ethanol; water at 80℃; for 4h; Suzuki-Miyaura Coupling;98%
4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

4-bromo-3-chloro-1H-indole
1216305-58-6

4-bromo-3-chloro-1H-indole

Conditions
ConditionsYield
With N-chloro-succinimide In N,N-dimethyl-formamide at 20℃; for 12h; Inert atmosphere;97%
With 1,3-dichloro-5,5-dimethylhydantoin In 1,4-dioxane at 25℃; for 3h;88%
4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

p-toluenesulfonylhydroxylamine
1593-60-8

p-toluenesulfonylhydroxylamine

4-bromo-3-(p-tolylthio)-1H-indole

4-bromo-3-(p-tolylthio)-1H-indole

Conditions
ConditionsYield
With 1-hydroxy-pyrrolidine-2,5-dione; iodine In butan-1-ol at 120℃; for 15h; Inert atmosphere; Sealed tube; regioselective reaction;97%
4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

formaldehyd
50-00-0

formaldehyd

dimethyl amine
124-40-3

dimethyl amine

4-bromogramine
64258-88-4

4-bromogramine

Conditions
ConditionsYield
In water; acetic acid for 48h; Ambient temperature;96.3%
With acetic acid In water at 0 - 25℃;
4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

carbon monoxide
201230-82-2

carbon monoxide

N-(1-methyl-2-phenylethyl)piperazine
14135-70-7

N-(1-methyl-2-phenylethyl)piperazine

(1H-indol-4-yl)-[4-(1-methyl-2-phenethyl)piperazin-1-yl]methanone

(1H-indol-4-yl)-[4-(1-methyl-2-phenethyl)piperazin-1-yl]methanone

Conditions
ConditionsYield
With 1,1'-bis-(diphenylphosphino)ferrocene; bis(benzonitrile)palladium(II) dichloride; triethylamine In toluene at 130℃; under 18751.5 Torr; for 20h;96%
4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

acetyl chloride
75-36-5

acetyl chloride

1-(4-bromo-1H-indol-3-yl)ethan-1-one
195874-03-4

1-(4-bromo-1H-indol-3-yl)ethan-1-one

Conditions
ConditionsYield
With tin(IV) chloride In toluene96%
With tin(IV) chloride In toluene at 0℃; for 2h; Friedel-Crafts reaction;95%
With tin(IV) chloride In toluene at 0℃; for 2h;75%
4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

thiophene-2-sulfonyl chloride
16629-19-9

thiophene-2-sulfonyl chloride

4-bromo-1-(2-thienylsulfonyl)-1H-indole
1001394-83-7

4-bromo-1-(2-thienylsulfonyl)-1H-indole

Conditions
ConditionsYield
With sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate In water for 25h;96%
4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

triisopropylsilyl chloride
13154-24-0

triisopropylsilyl chloride

4-Bromo-1-(tri-isopropylsilyl)-1H-indole
412048-44-3

4-Bromo-1-(tri-isopropylsilyl)-1H-indole

Conditions
ConditionsYield
Stage #1: 4-bromo-1H-indole With sodium hydride In tetrahydrofuran; mineral oil at 0 - 20℃; for 0.5h;
Stage #2: triisopropylsilyl chloride In tetrahydrofuran; mineral oil at 0 - 20℃;
96%
With sodium hydride In tetrahydrofuran at 0 - 20℃;88%
With sodium hydride In tetrahydrofuran at 20℃; Inert atmosphere; Cooling with ice;82%
With NaH In dichloromethane; N,N-dimethyl-formamide3.44 g (63%)
4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

benzenesulfonyl chloride
98-09-9

benzenesulfonyl chloride

1‐(benzenesulfonyl)‐4‐bromo‐1H‐indole
412048-77-2

1‐(benzenesulfonyl)‐4‐bromo‐1H‐indole

Conditions
ConditionsYield
With tetrabutylammomium bromide; sodium hydroxide In dichloromethane at 20℃; for 1h;95%
Stage #1: 4-bromo-1H-indole With sodium hydride In tetrahydrofuran at 0℃; for 1h;
Stage #2: benzenesulfonyl chloride In tetrahydrofuran at 20℃; for 2h;
93%
Stage #1: 4-bromo-1H-indole With sodium hydride In tetrahydrofuran at 20℃; for 1h;
Stage #2: benzenesulfonyl chloride In tetrahydrofuran for 1h;
87%
4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

2-Bromoethyl methyl ether
6482-24-2

2-Bromoethyl methyl ether

4-bromo-1-(2-methoxyethyl)-1H-indole

4-bromo-1-(2-methoxyethyl)-1H-indole

Conditions
ConditionsYield
Stage #1: 4-bromo-1H-indole With sodium hydride In 1,2-dimethoxyethane; dimethyl sulfoxide at 20℃; for 0.5h;
Stage #2: 2-Bromoethyl methyl ether In 1,2-dimethoxyethane; dimethyl sulfoxide at 20℃;
95%
4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

pyridine-3-sulfonyl chloride hydrochloride
42899-76-3

pyridine-3-sulfonyl chloride hydrochloride

4-bromo-1-(pyridine-3-ylsulfonyl)-1H-indole
1001394-86-0

4-bromo-1-(pyridine-3-ylsulfonyl)-1H-indole

Conditions
ConditionsYield
With sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate In water for 0.75h;95%
4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

benzaldehyde
100-52-7

benzaldehyde

C23H16Br2N2
1338069-91-2

C23H16Br2N2

Conditions
ConditionsYield
With C20H24Cl2N2O2Zr In ethanol at 25 - 27℃; for 0.416667h;95%
4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

3-pyridylboronic acid
1692-25-7

3-pyridylboronic acid

4-(pyridin-3-yl)-1H-indole
108378-92-3

4-(pyridin-3-yl)-1H-indole

Conditions
ConditionsYield
With bis(η3-allyl-μ-chloropalladium(II)); N,N,N′,N′-tetra(diphenylphosphinomethyl)-1,2-ethylenediamine; potassium carbonate In N,N-dimethyl acetamide; butan-1-ol at 110℃; for 20h; Suzuki Coupling; Inert atmosphere;95%
4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

C17H18O5

C17H18O5

C24H20BrNO4

C24H20BrNO4

Conditions
ConditionsYield
In acetonitrile at 70℃; for 0.5h;95%
4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

bromethyl methyl ether
13057-17-5

bromethyl methyl ether

C10H10BrNO
1531618-73-1

C10H10BrNO

Conditions
ConditionsYield
Stage #1: 4-bromo-1H-indole With sodium hydride In tetrahydrofuran; N,N-dimethyl-formamide; mineral oil at 0℃; for 1h; Inert atmosphere;
Stage #2: bromethyl methyl ether In tetrahydrofuran; N,N-dimethyl-formamide; mineral oil at 0 - 23℃; for 1h;
95%
4-bromo-1H-indole
52488-36-5

4-bromo-1H-indole

Benzenesulfinic acid
618-41-7

Benzenesulfinic acid

4-bromo-3-(phenylthio)-1H-indole
945000-87-3

4-bromo-3-(phenylthio)-1H-indole

Conditions
ConditionsYield
With tetra-(n-butyl)ammonium iodide; toluene-4-sulfonic acid In 1,2-dichloro-ethane at 80℃; for 12h; regioselective reaction;95%

52488-36-5Relevant articles and documents

Superhydrophobic nickel/carbon core-shell nanocomposites for the hydrogen transfer reactions of nitrobenzene and N-heterocycles

Duan, Zhiying,Liu, Fangfang,Pang, Shaofeng,Su, Qiong,Wang, Yanbin,Xie, Xin,Zhang, Ping,Zhang, Yujing,Zhou, Feng

, p. 1996 - 2010 (2020/04/07)

In this work, catalytic hydrogen transfer as an effective, green, convenient and economical strategy is for the first time used to synthesize anilines and N-heterocyclic aromatic compounds from nitrobenzene and N-heterocycles in one step. Nevertheless, how to effectively reduce the possible effects of water on the catalyst by removal of the by-product water, and to further introduce water as the solvent based on green chemistry are still challenges. Since the structures and properties of carbon nanocomposites are easily modified by controllable construction, a one step pyrolysis process is used for controllable construction of micro/nano hierarchical carbon nanocomposites with core-shell structures and magnetic separation performance. Using various characterization methods and model reactions the relationship between the structure of Ni?NCFs (nickel-nitrogen-doped carbon frameworks) and catalytic performance was investigated, and the results show that there is a positive correlation between the catalytic performance and hydrophobicity of catalysts. Besides, the possible catalytically active sites, which are formed by the interaction of pyridinic N and graphitic N in the structure of nitrogen-doped graphene with the surfaces of Ni nanoparticles, should be pivotal to achieving the relatively high catalytic performance of materials. Due to its unique structure, the obtained Ni?NCF-700 catalyst with superhydrophobicity shows extraordinary performances toward the hydrogen transfer reaction of nitrobenzene and N-heterocycles in the aqueous state; meanwhile, it was also found that Ni?NCF-700 still retained its excellent catalytic activity and structural integrity after three cycles. Compared with traditional catalytic systems, our catalytic systems offer a highly effective, green and economical alternative for nitrobenzene and N-heterocycle transformation, and may open up a new avenue for simple construction of structure and activity defined carbon nanocomposite heterogeneous catalysts with superhydrophobicity.

DMSO/t-BuONa/O2-Mediated Aerobic Dehydrogenation of Saturated N-Heterocycles

Cai, Hu,Tan, Wei,Xie, Yongfa,Yang, Ruchun,Yue, Shusheng

, p. 7501 - 7509 (2020/07/07)

Aromatic N-heterocycles such as quinolines, isoquinolines, and indolines are synthesized via sodium tert-butoxide-promoted oxidative dehydrogenation of the saturated heterocycles in DMSO solution. This reaction proceeds under mild reaction conditions and has a good functional group tolerance. Mechanistic studies suggest a radical pathway involving hydrogen abstraction of dimsyl radicals from the N-H bond or α-C-H of the substrates and subsequent oxidation of the nitrogen or α-aminoalkyl radicals.

Half-sandwich structured ruthenium complex and preparation method thereof, and method for reducing o-nitrobenzene ethanol compound into indole compound

-

Paragraph 0080; 0087, (2017/07/22)

The invention discloses a half-sandwich structured ruthenium complex and a preparation method thereof, and a method for reducing an o-nitrobenzene ethanol compound into an indole compound. The structure of the ruthenium complex is as shown in formula (A), wherein in the formula (A), X is halogen, R is H, -oxyl, halogen or nitro, and n is a positive integer ranging from 1 to 4. By the adoption of the preparation method, the ruthenium complex with excellent chemical stability can be obtained; meanwhile, the preparation method has the advantages of simple operation, low equipment requirement and batch production; furthermore, the ruthenium complex can be used as a catalyst for catalytically reducing the o-nitrobenzene ethanol compound (Refer to Specification).

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 52488-36-5