Welcome to LookChem.com Sign In|Join Free

CAS

  • or

57848-46-1

Post Buying Request

57848-46-1 Suppliers

Recommended suppliersmore

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

57848-46-1 Usage

Chemical Properties

lightyellowtobeigecrystal

Uses

Different sources of media describe the Uses of 57848-46-1 differently. You can refer to the following data:
1. 4-Bromo-2-fluorobenzaldehyde is used in the synthesis of Nigeglanine hydrobromide.
2. 4-Bromo-2-fluorobenzaldehyde is used in the preparation of nigeglanine hydrobromide.
3. 4-Bromo-2-fluorobenzaldehyde has been used in the preparation of:2-functionalized aromatic monoaldehydes, via reaction with different secondary amines and phenolfluorostilbenesbenzyl amine-based histamine H3 antagonist having serotonin reuptake activity6-bromo-2-(4-bromo-2-fluorophenyl)-2,3-dihydro-4H-chromen-4-one

Check Digit Verification of cas no

The CAS Registry Mumber 57848-46-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,8,4 and 8 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 57848-46:
(7*5)+(6*7)+(5*8)+(4*4)+(3*8)+(2*4)+(1*6)=171
171 % 10 = 1
So 57848-46-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H4BrFO/c8-6-2-1-5(4-10)7(9)3-6/h1-4H

57848-46-1 Well-known Company Product Price

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

  • (A16112)  4-Bromo-2-fluorobenzaldehyde, 97%   

  • 57848-46-1

  • 5g

  • 235.0CNY

  • Detail
  • Alfa Aesar

  • (A16112)  4-Bromo-2-fluorobenzaldehyde, 97%   

  • 57848-46-1

  • 25g

  • 1072.0CNY

  • Detail
  • Alfa Aesar

  • (A16112)  4-Bromo-2-fluorobenzaldehyde, 97%   

  • 57848-46-1

  • 100g

  • 3785.0CNY

  • Detail

57848-46-1SDS

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-2-fluorobenzaldehyde

1.2 Other means of identification

Product number -
Other names 4-bromo-6-fluorobenzaldehyde

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:57848-46-1 SDS

57848-46-1Synthetic route

2,5-dibromofluorobenzene
1435-52-5

2,5-dibromofluorobenzene

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

N,N-dimethyl-formamide

4-bromo-2-fluorobenzaldehyde
57848-46-1

4-bromo-2-fluorobenzaldehyde

Conditions
ConditionsYield
Stage #1: 2,5-dibromofluorobenzene With tri-n-butyllithium magnesate complex In tetrahydrofuran; toluene at 0℃; for 1h;
Stage #2: N,N-dimethyl-formamide In toluene at 0℃; for 0.5h;
Stage #3: With citric acid at 20℃;
92%
Stage #1: 2,5-dibromofluorobenzene With n-butyllithium In diethyl ether at -100℃; for 0.75h;
Stage #2: N,N-dimethyl-formamide In diethyl ether at -90℃; for 0.25h;
Stage #3: With sulfuric acid In diethyl ether; water at -50℃;
86%
Stage #1: 2,5-dibromofluorobenzene With isopropylmagnesium bromide In tetrahydrofuran at 0 - 5℃; for 1.5h;
Stage #2: N,N-dimethyl-formamide In tetrahydrofuran; toluene at 0 - 5℃; for 4h;
Stage #3: With acetic acid In tetrahydrofuran; water; toluene at 0 - 10℃;
4-bromo-2-fluorobenzyl alcohol
188582-62-9

4-bromo-2-fluorobenzyl alcohol

4-bromo-2-fluorobenzaldehyde
57848-46-1

4-bromo-2-fluorobenzaldehyde

Conditions
ConditionsYield
With tert.-butylhydroperoxide; tetrabutylammomium bromide In decane; benzene at 40℃; for 24h; Inert atmosphere; Sealed tube; chemoselective reaction;87%
aqueous sodium hydrogen sulfite

aqueous sodium hydrogen sulfite

2,5-dibromofluorobenzene
1435-52-5

2,5-dibromofluorobenzene

butyl magnesium bromide
693-04-9

butyl magnesium bromide

4-bromo-2-fluorobenzaldehyde
57848-46-1

4-bromo-2-fluorobenzaldehyde

Conditions
ConditionsYield
With n-butyllithium; acetic acid In tetrahydrofuran; hexane; N,N-dimethyl-formamide; toluene82%
4-bromo-3-fluorobenzyl alcohol
222978-01-0

4-bromo-3-fluorobenzyl alcohol

4-bromo-2-fluorobenzaldehyde
57848-46-1

4-bromo-2-fluorobenzaldehyde

Conditions
ConditionsYield
With sodium acetate; pyridinium chlorochromate In dichloromethane at 20℃; for 2h;63%
With sodium acetate; pyridinium chlorochromate In dichloromethane at 20℃; for 2h; light protection;63%
N-(4-bromo-2-fluoro-benzyl)-acetamide
877129-98-1

N-(4-bromo-2-fluoro-benzyl)-acetamide

4-bromo-2-fluorobenzaldehyde
57848-46-1

4-bromo-2-fluorobenzaldehyde

Conditions
ConditionsYield
With N-Bromosuccinimide In chloroform at 20℃; for 18h;51%
conc sulphuric acid

conc sulphuric acid

2-fluoro-4-bromotoluene
51436-99-8

2-fluoro-4-bromotoluene

sulfuric acid
7664-93-9

sulfuric acid

4-bromo-2-fluorobenzaldehyde
57848-46-1

4-bromo-2-fluorobenzaldehyde

Conditions
ConditionsYield
With acetic anhydride In ethanol; water; acetic acid
4-bromo-2-fluorobenzaldehyde oxime
202865-64-3

4-bromo-2-fluorobenzaldehyde oxime

4-bromo-2-fluorobenzaldehyde
57848-46-1

4-bromo-2-fluorobenzaldehyde

Conditions
ConditionsYield
With acetic anhydride In ethanol at 140℃;
3-fluorobromobenzene
1073-06-9

3-fluorobromobenzene

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

N,N-dimethyl-formamide

4-bromo-2-fluorobenzaldehyde
57848-46-1

4-bromo-2-fluorobenzaldehyde

Conditions
ConditionsYield
Stage #1: 3-fluorobromobenzene With lithium diisopropyl amide In tetrahydrofuran at -78℃;
Stage #2: N,N-dimethyl-formamide In tetrahydrofuran
4-bromo-3-fluorobenzoic acid
153556-42-4

4-bromo-3-fluorobenzoic acid

4-bromo-2-fluorobenzaldehyde
57848-46-1

4-bromo-2-fluorobenzaldehyde

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: sodium tetrahydroborate; boron trifluoride diethyl etherate / tetrahydrofuran / 2 h / 20 °C
2: sodium acetate; pyridinium chlorochromate / dichloromethane / 2 h / 20 °C
View Scheme
Multi-step reaction with 2 steps
1: sodium tetrahydroborate; boron trifluoride diethyl etherate / tetrahydrofuran / 2 h / 20 °C / Cooling with ice
2: sodium acetate; pyridinium chlorochromate / dichloromethane / 2 h / 20 °C / light protection
View Scheme
4-bromo-3-fluorotoluene
452-74-4

4-bromo-3-fluorotoluene

4-bromo-2-fluorobenzaldehyde
57848-46-1

4-bromo-2-fluorobenzaldehyde

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1.1: pyridine; water; potassium permanganate / 3 h / 90 °C
1.3: pH 2
2.1: sodium tetrahydroborate; boron trifluoride diethyl etherate / tetrahydrofuran / 2 h / 20 °C
3.1: sodium acetate; pyridinium chlorochromate / dichloromethane / 2 h / 20 °C
View Scheme
Multi-step reaction with 3 steps
1.1: potassium permanganate / pyridine; water / 3 h / 90 °C
1.2: pH 2
1.3: pH 2
2.1: sodium tetrahydroborate; boron trifluoride diethyl etherate / tetrahydrofuran / 2 h / 20 °C / Cooling with ice
3.1: sodium acetate; pyridinium chlorochromate / dichloromethane / 2 h / 20 °C / light protection
View Scheme
1-methyl-piperazine
109-01-3

1-methyl-piperazine

4-bromo-2-fluorobenzaldehyde
57848-46-1

4-bromo-2-fluorobenzaldehyde

4-bromo-2-(4-methylpiperazin-1-yl)benzaldehyde
628326-12-5

4-bromo-2-(4-methylpiperazin-1-yl)benzaldehyde

Conditions
ConditionsYield
With potassium carbonate In N,N-dimethyl-formamide at 100℃;100%
With potassium carbonate In N,N-dimethyl-formamide at 120℃; for 4h; Sealed tube;84%
4-bromo-2-fluorobenzaldehyde
57848-46-1

4-bromo-2-fluorobenzaldehyde

2-hydroxy-5-chloro-aniline
95-85-2

2-hydroxy-5-chloro-aniline

4-bromo-2-[(E)-(4-bromo-2-fluoro-phenyl)methyleneamino]phenol

4-bromo-2-[(E)-(4-bromo-2-fluoro-phenyl)methyleneamino]phenol

Conditions
ConditionsYield
In hydroxy acetylene at 60℃; for 1h;100%
ethylene glycol
107-21-1

ethylene glycol

4-bromo-2-fluorobenzaldehyde
57848-46-1

4-bromo-2-fluorobenzaldehyde

2-(4-bromo-2-fluorophenyl)-1,3-dioxolane
248270-23-7

2-(4-bromo-2-fluorophenyl)-1,3-dioxolane

Conditions
ConditionsYield
With toluene-4-sulfonic acid; orthoformic acid triethyl ester In 1,2-dichloro-ethane at 80℃; for 2.5h;100%
With toluene-4-sulfonic acid In ethanol; benzene for 3h; Heating / reflux;99%
With toluene-4-sulfonic acid In toluene for 2.5h; Heating / reflux;
toluene-4-sulfonic acid In toluene for 2.5h; Heating / reflux;
With orthoformic acid triethyl ester; toluene-4-sulfonic acid In 1,2-dichloro-ethane at 80℃; for 2.5h;
3-Bromopyridine
626-55-1

3-Bromopyridine

4-bromo-2-fluorobenzaldehyde
57848-46-1

4-bromo-2-fluorobenzaldehyde

C12H9BrFNO
1343705-99-6

C12H9BrFNO

Conditions
ConditionsYield
Stage #1: 3-Bromopyridine With n-butyllithium In diethyl ether; hexane at -78 - -60℃; for 0.5h;
Stage #2: 4-bromo-2-fluorobenzaldehyde In tetrahydrofuran; diethyl ether; hexane at -78 - -40℃; for 1h;
100%
N-Boc-1,3-diaminopropane
75178-96-0

N-Boc-1,3-diaminopropane

benzyl chloroformate
501-53-1

benzyl chloroformate

4-bromo-2-fluorobenzaldehyde
57848-46-1

4-bromo-2-fluorobenzaldehyde

benzyl 4-bromo-2-fluorobenzyl(3-((tert-butoxycarbonyl)amino)propyl)carbamate
1437800-85-5

benzyl 4-bromo-2-fluorobenzyl(3-((tert-butoxycarbonyl)amino)propyl)carbamate

Conditions
ConditionsYield
Stage #1: N-Boc-1,3-diaminopropane; 4-bromo-2-fluorobenzaldehyde With acetic acid In tetrahydrofuran for 0.5h;
Stage #2: With sodium tris(acetoxy)borohydride In tetrahydrofuran at 20℃;
Stage #3: benzyl chloroformate Further stages;
100%
morpholine
110-91-8

morpholine

4-bromo-2-fluorobenzaldehyde
57848-46-1

4-bromo-2-fluorobenzaldehyde

4-[(4-bromo-2-fluorophenyl)methyl]morpholine
338454-98-1

4-[(4-bromo-2-fluorophenyl)methyl]morpholine

Conditions
ConditionsYield
Stage #1: morpholine; 4-bromo-2-fluorobenzaldehyde In chloroform at 58 - 60℃; for 1h; Sealed tube;
Stage #2: With sodium tris(acetoxy)borohydride In chloroform at 58 - 60℃; for 16h; Sealed tube;
100%
Stage #1: morpholine; 4-bromo-2-fluorobenzaldehyde In chloroform at 58 - 60℃; for 1h; Sealed tube;
Stage #2: With sodium tris(acetoxy)borohydride In chloroform at 58 - 60℃; for 16h; Sealed tube;
Stage #1: morpholine; 4-bromo-2-fluorobenzaldehyde In chloroform at 58 - 60℃; for 1h; Sealed tube;
Stage #2: With sodium tris(acetoxy)borohydride In chloroform at 58 - 60℃; for 16h; Sealed tube;
100 %Spectr.
3-(3-amino-phenyl)-acrylic acid methyl ester
58186-45-1

3-(3-amino-phenyl)-acrylic acid methyl ester

4-bromo-2-fluorobenzaldehyde
57848-46-1

4-bromo-2-fluorobenzaldehyde

C17H13BrFNO2

C17H13BrFNO2

Conditions
ConditionsYield
With toluene-4-sulfonic acid In toluene at 110℃; for 24h; Dean-Stark;100%
(E)-methyl 3-(3-amino-5-fluorophenyl)acrylate
918811-47-9

(E)-methyl 3-(3-amino-5-fluorophenyl)acrylate

4-bromo-2-fluorobenzaldehyde
57848-46-1

4-bromo-2-fluorobenzaldehyde

C17H12BrF2NO2

C17H12BrF2NO2

Conditions
ConditionsYield
With toluene-4-sulfonic acid In toluene at 130℃; for 48h; Dean-Stark;100%
C14H23N5O

C14H23N5O

4-bromo-2-fluorobenzaldehyde
57848-46-1

4-bromo-2-fluorobenzaldehyde

C21H27BrFN5O

C21H27BrFN5O

Conditions
ConditionsYield
for 12h; Reflux;100%
4-bromo-2-fluorobenzaldehyde
57848-46-1

4-bromo-2-fluorobenzaldehyde

4-bromo-2-fluorobenzyl alcohol
188582-62-9

4-bromo-2-fluorobenzyl alcohol

Conditions
ConditionsYield
With methanol; sodium tetrahydroborate at -5 - 20℃;99%
With methanol; sodium tetrahydroborate at -5 - 23℃; for 1h;99%
With sodium tetrahydroborate In methanol at 20℃; for 0.5h;99%
methanol
67-56-1

methanol

4-bromo-2-fluorobenzaldehyde
57848-46-1

4-bromo-2-fluorobenzaldehyde

1-bromo-4-(dimethoxymethyl)-3-fluorobenzene
439814-87-6

1-bromo-4-(dimethoxymethyl)-3-fluorobenzene

Conditions
ConditionsYield
With hydrogenchloride at 20℃; for 2h;99%
With toluene-4-sulfonic acid for 14h; Heating / reflux;
ethylmagnesium iodide
10467-10-4

ethylmagnesium iodide

4-bromo-2-fluorobenzaldehyde
57848-46-1

4-bromo-2-fluorobenzaldehyde

1-(4-bromo-2-fluorophenyl)propan-1-ol
1214900-59-0

1-(4-bromo-2-fluorophenyl)propan-1-ol

Conditions
ConditionsYield
In diethyl ether at 20℃; for 12h; Cooling with ice;99%
isopropylmagnesium bromide
920-39-8

isopropylmagnesium bromide

4-bromo-2-fluorobenzaldehyde
57848-46-1

4-bromo-2-fluorobenzaldehyde

1-(4-bromo-2-fluorophenyl)-2-methylpropan-1-ol
1332651-40-7

1-(4-bromo-2-fluorophenyl)-2-methylpropan-1-ol

Conditions
ConditionsYield
Stage #1: isopropylmagnesium bromide; 4-bromo-2-fluorobenzaldehyde In diethyl ether at 20℃; for 12h; Cooling with ice;
Stage #2: With hydrogenchloride In diethyl ether; water
99%
1-(4-methoxyphenyl)ethanone
100-06-1

1-(4-methoxyphenyl)ethanone

4-bromo-2-fluorobenzaldehyde
57848-46-1

4-bromo-2-fluorobenzaldehyde

(E)-1-(4-methoxyphenyl)-3-(4-bromo-2-fluorophenyl)prop-2-en-1-one

(E)-1-(4-methoxyphenyl)-3-(4-bromo-2-fluorophenyl)prop-2-en-1-one

Conditions
ConditionsYield
Stage #1: 1-(4-methoxyphenyl)ethanone With sodium hydroxide In ethanol; water at 20℃; for 0.0833333h; Claisen-Schmidt Condensation;
Stage #2: 4-bromo-2-fluorobenzaldehyde at 20℃; Claisen-Schmidt Condensation;
99%
(2-nitroethenyl)benzene
102-96-5

(2-nitroethenyl)benzene

3-amino-1-benzylindolin-2-one hydrochloride
1324055-93-7

3-amino-1-benzylindolin-2-one hydrochloride

4-bromo-2-fluorobenzaldehyde
57848-46-1

4-bromo-2-fluorobenzaldehyde

(2'S,3'S,4'S,5'S)-1-benzyl-5'-(4-bromo-2-fluorophenyl)-4'-nitro-3'-phenylspiro[indoline-3,2'-pyrrolidin]-2-one

(2'S,3'S,4'S,5'S)-1-benzyl-5'-(4-bromo-2-fluorophenyl)-4'-nitro-3'-phenylspiro[indoline-3,2'-pyrrolidin]-2-one

Conditions
ConditionsYield
Stage #1: 3-amino-1-benzylindolin-2-one hydrochloride With sodium hydrogencarbonate In toluene at 25℃; for 0.333333h; Schlenk technique; Inert atmosphere;
Stage #2: In toluene at 25℃; for 0.333333h; Schlenk technique; Inert atmosphere; Molecular sieve;
Stage #3: (2-nitroethenyl)benzene; 4-bromo-2-fluorobenzaldehyde With (R)-3,3'-bis(2,4,6-triisopropylphenyl)binol phosphoric acid In toluene at 25℃; Schlenk technique; Inert atmosphere; Molecular sieve; enantioselective reaction;
99%
(trifluoromethyl)trimethylsilane
81290-20-2

(trifluoromethyl)trimethylsilane

4-bromo-2-fluorobenzaldehyde
57848-46-1

4-bromo-2-fluorobenzaldehyde

1-(4-bromo-2-fluorophenyl)-2,2,2-trifluoroethanol
1033805-88-7

1-(4-bromo-2-fluorophenyl)-2,2,2-trifluoroethanol

Conditions
ConditionsYield
Stage #1: (trifluoromethyl)trimethylsilane; 4-bromo-2-fluorobenzaldehyde With tetrabutyl ammonium fluoride In tetrahydrofuran at 0 - 20℃; for 3.16667h; Inert atmosphere;
Stage #2: With hydrogenchloride In tetrahydrofuran; water Inert atmosphere;
98%
With tetrabutyl ammonium fluoride In tetrahydrofuran at 0 - 20℃; for 3.16667h; Inert atmosphere;98%
Stage #1: (trifluoromethyl)trimethylsilane; 4-bromo-2-fluorobenzaldehyde With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 4h;
Stage #2: With water In N,N-dimethyl-formamide for 4h; Acidic conditions;
93%
ethyl 2-sulfanylacetate
623-51-8

ethyl 2-sulfanylacetate

4-bromo-2-fluorobenzaldehyde
57848-46-1

4-bromo-2-fluorobenzaldehyde

6-Brombenzothiophen-2-carbonsaeure-ethylester
105191-64-8

6-Brombenzothiophen-2-carbonsaeure-ethylester

Conditions
ConditionsYield
Stage #1: ethyl 2-sulfanylacetate; 4-bromo-2-fluorobenzaldehyde With potassium carbonate In N,N-dimethyl-formamide at 0 - 20℃; Inert atmosphere;
Stage #2: In N,N-dimethyl-formamide at 60℃; for 5.5h;
98%
With potassium carbonate In N,N-dimethyl-formamide at 0 - 60℃; for 22.5h; Inert atmosphere;97%
With triethylamine In dimethyl sulfoxide at 75 - 80℃; for 2 - 3h; Product distribution / selectivity;92%
tert-butylamine
75-64-9

tert-butylamine

4-bromo-2-fluorobenzaldehyde
57848-46-1

4-bromo-2-fluorobenzaldehyde

(4-bromo-2-fluoro-benzylidene)-tert-butyl-amine
1227466-98-9

(4-bromo-2-fluoro-benzylidene)-tert-butyl-amine

Conditions
ConditionsYield
In dichloromethane at 20℃; for 48h; Product distribution / selectivity; Dehydrating agent;98%
With magnesium sulfate In dichloromethane for 48h;98%
phenylacetylene
536-74-3

phenylacetylene

4-bromo-2-fluorobenzaldehyde
57848-46-1

4-bromo-2-fluorobenzaldehyde

(S)-1-(4-bromo-2-fluorophenyl)-3-phenylprop-2-yn-1-ol

(S)-1-(4-bromo-2-fluorophenyl)-3-phenylprop-2-yn-1-ol

Conditions
ConditionsYield
With C50H50N4RhS2(1+)*F6P(1-); triethylamine In N,N-dimethyl acetamide at 20℃; for 24h; Reagent/catalyst; Schlenk technique; Inert atmosphere; Sealed tube; enantioselective reaction;98%
sodium carbonate
497-19-8

sodium carbonate

4-bromo-2-fluorobenzaldehyde
57848-46-1

4-bromo-2-fluorobenzaldehyde

1-bromo-4-(dimethoxymethyl)-3-fluorobenzene
439814-87-6

1-bromo-4-(dimethoxymethyl)-3-fluorobenzene

Conditions
ConditionsYield
With p-toluenesulfonic acid monohydrate In methanol97%
4-bromo-2-fluorobenzaldehyde
57848-46-1

4-bromo-2-fluorobenzaldehyde

2-(4-bromo-2-fluorophenyl)-1,3-dioxolane
248270-23-7

2-(4-bromo-2-fluorophenyl)-1,3-dioxolane

Conditions
ConditionsYield
With toluene-4-sulfonic acid In ethylene glycol; toluene97%
anthranilic acid amide
28144-70-9

anthranilic acid amide

4-bromo-2-fluorobenzaldehyde
57848-46-1

4-bromo-2-fluorobenzaldehyde

2-(4-bromo-2-fluorophenyl)-2,3-dihydroquinazolin-4(1H)-one

2-(4-bromo-2-fluorophenyl)-2,3-dihydroquinazolin-4(1H)-one

Conditions
ConditionsYield
With Indion Ina 225H resin In methanol at 20℃; for 2h; Green chemistry;97%
acetic anhydride
108-24-7

acetic anhydride

4-bromo-2-fluorobenzaldehyde
57848-46-1

4-bromo-2-fluorobenzaldehyde

(4-bromo-2-fluorophenyl)methylene diacetate

(4-bromo-2-fluorophenyl)methylene diacetate

Conditions
ConditionsYield
With tungstate sulfuric acid In neat (no solvent) at 20℃; for 0.0833333h; Green chemistry;97%
2-Hydroxy-1,4-naphthoquinone
83-72-7

2-Hydroxy-1,4-naphthoquinone

4-bromo-2-fluorobenzaldehyde
57848-46-1

4-bromo-2-fluorobenzaldehyde

C27H12BrFO5

C27H12BrFO5

Conditions
ConditionsYield
With silica-supported tungstic acid In neat (no solvent) at 60℃; for 0.0666667h; Sonication; Green chemistry;97%
4-bromo-2-fluorobenzaldehyde
57848-46-1

4-bromo-2-fluorobenzaldehyde

4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane
25015-63-8

4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane

2-((4-bromo-2-fluorobenzyl)oxy)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

2-((4-bromo-2-fluorobenzyl)oxy)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Conditions
ConditionsYield
With C19H25AsN2O In benzene-d6 at 20℃; for 0.5h; Inert atmosphere; Glovebox; Schlenk technique;97%
ethylenediamine
107-15-3

ethylenediamine

4-bromo-2-fluorobenzaldehyde
57848-46-1

4-bromo-2-fluorobenzaldehyde

2-(4-bromo-2-fluorophenyl)-4,5-dihydro-1H-imidazole

2-(4-bromo-2-fluorophenyl)-4,5-dihydro-1H-imidazole

Conditions
ConditionsYield
With iodine; potassium carbonate In tert-butyl alcohol at 70℃; for 3.5h;97%
sodium chlorite
7758-19-2

sodium chlorite

Na2HPO4.12H2O

Na2HPO4.12H2O

4-bromo-2-fluorobenzaldehyde
57848-46-1

4-bromo-2-fluorobenzaldehyde

2-fluoro-4-bromobenzoic acid
112704-79-7

2-fluoro-4-bromobenzoic acid

Conditions
ConditionsYield
With dihydrogen peroxide In water; acetonitrile96%
acrylic acid methyl ester
292638-85-8

acrylic acid methyl ester

4-bromo-2-fluorobenzaldehyde
57848-46-1

4-bromo-2-fluorobenzaldehyde

(E)-methyl 3-(3-fluoro-4-formylphenyl)acrylate
208036-32-2

(E)-methyl 3-(3-fluoro-4-formylphenyl)acrylate

Conditions
ConditionsYield
With palladium diacetate; potassium carbonate; triphenylphosphine In N,N-dimethyl-formamide at 80℃; for 12h; Inert atmosphere;96%
Stage #1: 4-bromo-2-fluorobenzaldehyde With N-Methyldicyclohexylamine; tris-(dibenzylideneacetone)dipalladium(0); tri tert-butylphosphoniumtetrafluoroborate In 1,4-dioxane for 0.5h; Microwave irradiation; Sealed vessel; Inert atmosphere;
Stage #2: acrylic acid methyl ester at 100℃; for 0.5h; Sealed vessel; Microwave irradiation;
80%
Stage #1: 4-bromo-2-fluorobenzaldehyde With N-Methyldicyclohexylamine; tri tert-butylphosphoniumtetrafluoroborate; tris-(dibenzylideneacetone)dipalladium(0) In 1,4-dioxane for 0.5h; Inert atmosphere; Sealed vial; Microwave irradiation;
Stage #2: acrylic acid methyl ester In 1,4-dioxane at 100℃; for 0.5h; Microwave irradiation;
80%
With palladium diacetate; triethylamine; tris-(o-tolyl)phosphine In N,N-dimethyl-formamide at 80℃; for 16h; Inert atmosphere;77%
With palladium diacetate; triethylamine; tris-(o-tolyl)phosphine In N,N-dimethyl acetamide at 100 - 110℃; for 6h;71%
4-bromo-2-fluorobenzaldehyde
57848-46-1

4-bromo-2-fluorobenzaldehyde

bis(pinacol)diborane
73183-34-3

bis(pinacol)diborane

2-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolane-2-yl)benzaldehyde
503176-50-9

2-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolane-2-yl)benzaldehyde

Conditions
ConditionsYield
With 1,1'-bis-(diphenylphosphino)ferrocene; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium acetate In 1,4-dioxane at 85℃; for 13h; Inert atmosphere;96%
With 1,1'-bis-(diphenylphosphino)ferrocene; palladium bis[bis(diphenylphosphino)ferrocene] dichloride; potassium acetate In 1,4-dioxane; water at 85℃; for 13h; Inert atmosphere;96%
2-Hydroxy-1,4-naphthoquinone
83-72-7

2-Hydroxy-1,4-naphthoquinone

1,3-cylohexanedione
504-02-9

1,3-cylohexanedione

4-bromo-2-fluorobenzaldehyde
57848-46-1

4-bromo-2-fluorobenzaldehyde

C23H14BrFO4

C23H14BrFO4

Conditions
ConditionsYield
With silica-supported tungstic acid In neat (no solvent) at 60℃; for 0.05h; Sonication; Green chemistry;96%

57848-46-1Relevant articles and documents

Synthesis and Transformations of Functionalized Benzosiloxaboroles

Czub, Maja,Durka, Krzysztof,Luliński, Sergiusz,?osiewicz, Justyna,Serwatowski, Janusz,Urban, Mateusz,Wo?niak, Krzysztof

, p. 818 - 826 (2017/02/15)

The synthesis and characterization of a series of fluorinated benzosiloxaboroles bearing synthetically useful formyl and cyano groups is reported. These compounds have been obtained by multistep syntheses starting with simple halogenated benzenes. The general synthetic protocol was based on the generation of ortho-boronated aryldimethylsilanes which undergo dehydrogenative cyclization upon hydrolytic workup due to activation of the Si–H bond by the adjacent boronic group. In some cases the synergy of adjacent boron- and silicon-based functionalities resulted in an unexpected hydrosilylation of the CHO group under mild aqueous conditions. The reduction of a benzosiloxaborole derivative bearing the formyl group at the ortho position with respect to the boron atom resulted in a structural transformation reflecting the higher stability of the carboxaborole heterocycle with respect to its silicon counterpart. Thus, a unique heterocyclic system featuring a central 10-membered ring comprising two borasiloxane linkages was isolated.

HISTONE DEACETYLASE INHIBITORS

-

, (2012/05/04)

The disclosure provides compounds of formula I and methods for preparation thereof. The compounds act as inhibitor of histone deacetylase.

HISTONE DEACETYLASE INHIBITORS

-

, (2011/04/13)

The disclosure provides compounds of formula I and methods for preparation thereof. The compounds act as inhibitor of histone deacetylase.

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 57848-46-1