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626-40-4

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626-40-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 626-40-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 626-40:
(5*6)+(4*2)+(3*6)+(2*4)+(1*0)=64
64 % 10 = 4
So 626-40-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H5Br2N/c7-4-1-5(8)3-6(9)2-4/h1-3H,9H2

626-40-4SDS

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 3,5-Dibromoaniline

1.2 Other means of identification

Product number -
Other names 3,5-dibromo-benzenamine

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:626-40-4 SDS

626-40-4Synthetic route

3,5-dibromonitrobenzene
6311-60-0

3,5-dibromonitrobenzene

3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

Conditions
ConditionsYield
With hydrogenchloride; tin at 90℃; for 7h;99%
With hydrogenchloride; hydrogen; nickel In ethanol96%
Stage #1: 3,5-dibromonitrobenzene With tin(II) chloride dihdyrate In tetrahydrofuran; methanol at 60℃; for 20h;
Stage #2: With water; sodium hydroxide for 2h;
90%
1,3,5-trisbromobenzene
626-39-1

1,3,5-trisbromobenzene

3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

Conditions
ConditionsYield
With bis(triphenylphosphine)nickel(II) chloride; lithium hexamethyldisilazane In toluene at 100℃; for 2h; Glovebox; Sealed tube;81%
3,5-dibromophenylboronic acid

3,5-dibromophenylboronic acid

3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

Conditions
ConditionsYield
With O-(2,4-dinitrophenyl)hydroxylamine In toluene at 100℃; for 30h; Inert atmosphere;56%
hydrogenchloride
7647-01-0

hydrogenchloride

N,N'-bis-(3,5-dibromo-phenyl)-hydrazine
5326-51-2

N,N'-bis-(3,5-dibromo-phenyl)-hydrazine

A

3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

B

3,3′,5,5′-tetrabromo-1,1′-azobenzene
38292-74-9

3,3′,5,5′-tetrabromo-1,1′-azobenzene

Conditions
ConditionsYield
at 150℃; im Rohr;
N,N'-bis-(3,5-dibromo-phenyl)-hydrazine
5326-51-2

N,N'-bis-(3,5-dibromo-phenyl)-hydrazine

sulfuric acid
7664-93-9

sulfuric acid

A

3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

B

2,6,2',6'-tetrabromo-benzidine
860599-94-6

2,6,2',6'-tetrabromo-benzidine

C

4,6,2',6'-tetrabromo-biphenyl-2,4'-diyldiamine
854242-36-7

4,6,2',6'-tetrabromo-biphenyl-2,4'-diyldiamine

D

3,3′,5,5′-tetrabromo-1,1′-azobenzene
38292-74-9

3,3′,5,5′-tetrabromo-1,1′-azobenzene

3,5-dibromonitrobenzene
6311-60-0

3,5-dibromonitrobenzene

acid

acid

3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

Conditions
ConditionsYield
bei der Reduktion;
ethanol
64-17-5

ethanol

3,5-dibromonitrobenzene
6311-60-0

3,5-dibromonitrobenzene

Na2S2

Na2S2

A

3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

B

bis-(3,5-dibromo-phenyl)-diazene-N-oxide

bis-(3,5-dibromo-phenyl)-diazene-N-oxide

2,6-dibromo-4-nitroaniline
827-94-1

2,6-dibromo-4-nitroaniline

3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1.1: NaNO2; H2SO4; aq. H3PO4 / 2 h
1.2: urea; H2SO4; aq. H3PO4 / 20 °C
1.3: 85 percent / H2SO4; aq. H3PO4 / 0 - 20 °C
2.1: 99 percent / tin; aq. HCl / 7 h / 90 °C
View Scheme
Multi-step reaction with 2 steps
1: 80 percent / H2SO4; NaNO2 / ethanol / 36 h / 90 °C
2: 89 percent / SnCl2*2H2O / ethanol; tetrahydrofuran / 20 h / 20 °C
View Scheme
Multi-step reaction with 2 steps
1: 97 percent / NaNO2, H2SO4 / ethanol
2: 96 percent / 1.) H2; 2.) aq. HCl / Raney Ni / ethanol
View Scheme
4-nitro-aniline
100-01-6

4-nitro-aniline

3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 97 percent / Br2 / acetic acid / 4 h / 65 °C
2: 80 percent / H2SO4; NaNO2 / ethanol / 36 h / 90 °C
3: 89 percent / SnCl2*2H2O / ethanol; tetrahydrofuran / 20 h / 20 °C
View Scheme
Multi-step reaction with 3 steps
1: diluted hydrochloric acid; bromine
3: tin; hydrochloric acid
View Scheme
Multi-step reaction with 3 steps
1: aqueous sulfuric acid; bromine
3: iron; diluted sulfuric acid
View Scheme
Multi-step reaction with 3 steps
1.1: acetic acid; bromine / 4 h / 65 °C
2.1: sulfuric acid; sodium nitrite / ethanol / 40 h / 80 °C
3.1: tin(II) chloride dihdyrate / methanol; tetrahydrofuran / 20 h / 60 °C
3.2: 2 h
View Scheme
4-nitro-aniline
100-01-6

4-nitro-aniline

4-nitro-toluenediazonium sulfate-(2)

4-nitro-toluenediazonium sulfate-(2)

3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 98 percent / Br2 / acetic acid
2: 97 percent / NaNO2, H2SO4 / ethanol
3: 96 percent / 1.) H2; 2.) aq. HCl / Raney Ni / ethanol
View Scheme
4-nitro-aniline
100-01-6

4-nitro-aniline

Rest of peptide structure not given

Rest of peptide structure not given

3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

1,3-dibromobenzene
108-36-1

1,3-dibromobenzene

3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

Conditions
ConditionsYield
Multi-step reaction with 7 steps
1: beim Nitrieren
2: alcohol; ammonia / 160 °C
3: hydrochloric acid; bromine
5: alcohol; ammonia / 150 °C
7: tin; hydrochloric acid
View Scheme
1,3-dibromo-2-methoxy-5-nitrobenzene
31106-74-8

1,3-dibromo-2-methoxy-5-nitrobenzene

3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: alcohol; ammonia / 180 °C
3: tin; hydrochloric acid
View Scheme
1,2,3-tribromo-5-nitrobenzene
3460-20-6

1,2,3-tribromo-5-nitrobenzene

3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: alcohol; ammonia / 150 °C
3: tin; hydrochloric acid
View Scheme
4-bromo-1,2-dinitrobenzene
610-38-8

4-bromo-1,2-dinitrobenzene

3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

Conditions
ConditionsYield
Multi-step reaction with 6 steps
1: alcohol; ammonia / >180
2: hydrochloric acid; bromine
4: alcohol; ammonia / 150 °C
6: tin; hydrochloric acid
View Scheme
2,4-dibromonitrobenzene
51686-78-3

2,4-dibromonitrobenzene

3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

Conditions
ConditionsYield
Multi-step reaction with 6 steps
1: alcohol; ammonia / 160 °C
2: hydrochloric acid; bromine
4: alcohol; ammonia / 150 °C
6: tin; hydrochloric acid
View Scheme
2,3,5-tribromonitrobenzene
116529-58-9

2,3,5-tribromonitrobenzene

3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: alcohol; ammonia / 140 °C
3: tin; hydrochloric acid
View Scheme
5-bromo-2-nitroaniline
5228-61-5

5-bromo-2-nitroaniline

3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

Conditions
ConditionsYield
Multi-step reaction with 5 steps
1: hydrochloric acid; bromine
3: alcohol; ammonia / 150 °C
5: tin; hydrochloric acid
View Scheme
2,4-dibromo-6-nitroaniline
827-23-6

2,4-dibromo-6-nitroaniline

3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

Conditions
ConditionsYield
Multi-step reaction with 2 steps
2: tin; hydrochloric acid
View Scheme
2,3,4-tribromo-6-nitro-aniline

2,3,4-tribromo-6-nitro-aniline

3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

Conditions
ConditionsYield
Multi-step reaction with 4 steps
2: alcohol; ammonia / 150 °C
4: tin; hydrochloric acid
View Scheme
4,6-dibromo-2-nitroanisole
725241-64-5

4,6-dibromo-2-nitroanisole

3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: alcohol; ammonia / 170 °C
3: tin; hydrochloric acid
View Scheme
2-nitro-aniline
88-74-4

2-nitro-aniline

3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: Bromieren
3: tin; hydrochloric acid
View Scheme
Acetanilid
103-84-4

Acetanilid

3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: nitric acid / Verseifen das entstandene Gemisch mit Kalilauge und destillieren mit Wasserdampf
2: Bromieren
4: tin; hydrochloric acid
View Scheme
1,2-Dinitrobenzene
528-29-0

1,2-Dinitrobenzene

3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: alcoholic ammonium sulfide
2: Bromieren
4: tin; hydrochloric acid
View Scheme
benzene
71-43-2

benzene

3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

Conditions
ConditionsYield
Multi-step reaction with 5 steps
1: concentrated sulfuric acid; fuming nitric acid
2: alcoholic ammonium sulfide
3: Bromieren
5: tin; hydrochloric acid
View Scheme
3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

1,3,5-triaminobenzene
108-72-5

1,3,5-triaminobenzene

Conditions
ConditionsYield
With C24H12Cu2F9N4O7; tetrabutylammomium bromide; ammonia; caesium carbonate In water at 110 - 140℃; for 16h;100%
sodium 2'‐(dicyclohexylphosphaneyl)‐2,6‐diisopropyl‐[1,1'‐biphenyl]‐3‐sulfonate

sodium 2'‐(dicyclohexylphosphaneyl)‐2,6‐diisopropyl‐[1,1'‐biphenyl]‐3‐sulfonate

bis[(trimethylsilyl)methyl](1,5-cyclooctadiene)palladium(II)
225931-80-6

bis[(trimethylsilyl)methyl](1,5-cyclooctadiene)palladium(II)

3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

C58H73Br2NO10P2Pd2S2(2-)*2Na(1+)

C58H73Br2NO10P2Pd2S2(2-)*2Na(1+)

Conditions
ConditionsYield
In tetrahydrofuran at 20℃; for 1h;99%
β-D-glucose
492-61-5

β-D-glucose

3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

(-)-(3R,4S,5S,6R)-2-(3,5-dibromophenylamino)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol

(-)-(3R,4S,5S,6R)-2-(3,5-dibromophenylamino)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol

Conditions
ConditionsYield
In methanol for 12h; Reflux;97%
3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

acetic anhydride
108-24-7

acetic anhydride

acetic acid-(3,5-dibromo-anilide)
119430-40-9

acetic acid-(3,5-dibromo-anilide)

Conditions
ConditionsYield
With potassium carbonate In dichloromethane at 20℃;96%
formaldehyd
50-00-0

formaldehyd

3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

3,5-dibromo-N,N-dimethylaniline
64230-29-1

3,5-dibromo-N,N-dimethylaniline

Conditions
ConditionsYield
Stage #1: formaldehyd With sulfuric acid In tetrahydrofuran; water at 0℃; for 0.166667h; Inert atmosphere;
Stage #2: 3,5-dibromoaniline With sodium tetrahydroborate In tetrahydrofuran; water at 0 - 20℃; for 2h; Inert atmosphere;
96%
3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

4-carboxyphenylboronic acid
14047-29-1

4-carboxyphenylboronic acid

C20H15NO4

C20H15NO4

Conditions
ConditionsYield
Stage #1: 3,5-dibromoaniline; 4-carboxyphenylboronic acid With potassium carbonate In water; acetonitrile for 1h; Schlenk technique; Inert atmosphere;
Stage #2: With bis-triphenylphosphine-palladium(II) chloride In water; acetonitrile at 100℃; for 48h; Schlenk technique; Inert atmosphere; Sealed tube;
96%
With bis-triphenylphosphine-palladium(II) chloride; potassium carbonate In water; acetonitrile at 100℃; for 48h; Sealed tube; Inert atmosphere;79%
3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

C6H3Br2NOS
406935-63-5

C6H3Br2NOS

Conditions
ConditionsYield
With thionyl chloride Michaelis reaction;95%
formaldehyd
50-00-0

formaldehyd

3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

1,5-Bis(3,5-dibromphenyl)-3,7-dioxa-1,5-diazacyclooctan
77767-17-0

1,5-Bis(3,5-dibromphenyl)-3,7-dioxa-1,5-diazacyclooctan

Conditions
ConditionsYield
With sulfuric acid In 1,4-dioxane; water for 2h; Ambient temperature;91%
3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

2-Methoxybenzoyl chloride
21615-34-9

2-Methoxybenzoyl chloride

2-methoxy-N-(3,5-dibromophenyl)benzamide

2-methoxy-N-(3,5-dibromophenyl)benzamide

Conditions
ConditionsYield
In tetrahydrofuran for 1h;91%
3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

Benzoyl isothiocyanate
532-55-8

Benzoyl isothiocyanate

1-benzoyl-3-(3,5-dibromophenyl)thiourea
1000289-38-2

1-benzoyl-3-(3,5-dibromophenyl)thiourea

Conditions
ConditionsYield
In acetone at 20℃; for 0.5h;90%
3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

3,4,5-trimethoxyphenylboronic Acid
182163-96-8

3,4,5-trimethoxyphenylboronic Acid

5‘-amino-3,3“,4,4“,5,5“-hexamethoxy-1,1‘:3‘,1“-terphenyl

5‘-amino-3,3“,4,4“,5,5“-hexamethoxy-1,1‘:3‘,1“-terphenyl

Conditions
ConditionsYield
With bis-triphenylphosphine-palladium(II) chloride; potassium carbonate In 1,4-dioxane; water Reflux;90%
3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

2-trifluoromethylbenzoyl chloride
312-94-7

2-trifluoromethylbenzoyl chloride

2-trifluoromethyl-N-(3,5-dibromophenyl)benzamide

2-trifluoromethyl-N-(3,5-dibromophenyl)benzamide

Conditions
ConditionsYield
In tetrahydrofuran for 1h;88%
formic acid
64-18-6

formic acid

3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

N-(3,5-dibromophenyl)formamide
16582-45-9

N-(3,5-dibromophenyl)formamide

Conditions
ConditionsYield
Reflux;87%
3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

glycerol
56-81-5

glycerol

5,7-dibromoquinoline
34522-69-5

5,7-dibromoquinoline

Conditions
ConditionsYield
With sulfuric acid; sodium 3-nitrobenzenesulfonate at 100 - 135℃; for 3h;87%
Stage #1: 3,5-dibromoaniline With methanesulfonic acid; iron(ll)sulfate heptahydrate; sodium 3-nitrobenzenesulfonate at 120℃;
Stage #2: glycerol at 130℃; Skraup Quinoline Synthesis;
56%
With sulfuric acid; nitrobenzene
benzene-1,3-dicarboxylethylester-5-boronic acid
932378-94-4

benzene-1,3-dicarboxylethylester-5-boronic acid

3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

3′-amino-1,1′:4′,1″-terphenyl-3,3″,5,5″-tetracarboxylate

3′-amino-1,1′:4′,1″-terphenyl-3,3″,5,5″-tetracarboxylate

Conditions
ConditionsYield
With palladium diacetate; sodium carbonate In water; N,N-dimethyl-formamide at 60℃; Inert atmosphere;86%
iodobenzene
591-50-4

iodobenzene

3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

N'-phenyl-(1,1';3',1'-terphenyl)-5'-amine
63006-66-6

N'-phenyl-(1,1';3',1'-terphenyl)-5'-amine

Conditions
ConditionsYield
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate In tetrahydrofuran; water at 80℃; for 5h;86%
3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

benzoyl chloride
98-88-4

benzoyl chloride

N-(3,5-dibromophenyl)benzamide

N-(3,5-dibromophenyl)benzamide

Conditions
ConditionsYield
With pyridine In dichloromethane for 18h;85%
3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

cyclopropylboronic acid
411235-57-9

cyclopropylboronic acid

3,5-dicyclopropylaniline
41381-24-2

3,5-dicyclopropylaniline

Conditions
ConditionsYield
With tricyclohexylphosphine In water; toluene at 20 - 100℃; for 18h; Inert atmosphere;85%
3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

benzenesulfonyl chloride
98-09-9

benzenesulfonyl chloride

N-(3,5-dibromophenyl)benzenesulfonamide

N-(3,5-dibromophenyl)benzenesulfonamide

Conditions
ConditionsYield
With pyridine In dichloromethane for 18h;83%
With pyridine; acetone
With sodium acetate; acetic acid
2,4-dichloro-6-ethyl-1,3,5-triazine
698-72-6

2,4-dichloro-6-ethyl-1,3,5-triazine

3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

2-ethyl-4,6-bis[(3,5-dibromophenyl)amino]-1,3,5-triazine

2-ethyl-4,6-bis[(3,5-dibromophenyl)amino]-1,3,5-triazine

Conditions
ConditionsYield
In tetrahydrofuran for 18h; Reflux;83%
3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

1,3-dibromo-5-iodobenzene
19752-57-9

1,3-dibromo-5-iodobenzene

Conditions
ConditionsYield
With hydrogenchloride; potassium iodide; sodium nitrite In water; acetonitrile at 0℃;82%
Stage #1: 3,5-dibromoaniline With sulfuric acid; sodium nitrite at 0 - 50℃;
Stage #2: With potassium iodide In water at 0 - 80℃; for 1.25h;
80%
Stage #1: 3,5-dibromoaniline With phosphoric acid; sulfuric acid; sodium nitrite at 0 - 20℃;
Stage #2: With sulfuric acid; urea; potassium iodide; phosphoric acid at 20 - 50℃;
72%
Stage #1: 3,5-dibromoaniline With sulfuric acid; sodium nitrite at 0℃; for 2h;
Stage #2: With potassium iodide at 80℃; for 0.25h; Sandmeyer reaction;
70%
Diazotization;
3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

p-ethoxycarbonylphenylboronic acid
4334-88-7

p-ethoxycarbonylphenylboronic acid

C24H23NO4

C24H23NO4

Conditions
ConditionsYield
With tetrakis(triphenylphosphine) palladium(0); sodium carbonate In tetrahydrofuran at 80℃; for 72h; Schlenk technique; Inert atmosphere;82%
3,5-dichlorobenzoyl chloride
2905-62-6

3,5-dichlorobenzoyl chloride

3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

3,5-dichloro-N-(3,5-dibromophenyl)benzamide

3,5-dichloro-N-(3,5-dibromophenyl)benzamide

Conditions
ConditionsYield
In tetrahydrofuran for 1h;81%
2-amino-6-methyl-4-chloropyrimidine
5600-21-5

2-amino-6-methyl-4-chloropyrimidine

3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

N4-(3,5-dibromophenyl)-6-methylpyrimidine-2,4-diamine

N4-(3,5-dibromophenyl)-6-methylpyrimidine-2,4-diamine

Conditions
ConditionsYield
With hydrogenchloride In ethanol; water at 140℃; for 1.5h; Microwave irradiation; Sealed tube;81%
3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

3-aminophenylboronic acid hydrochloric salt

3-aminophenylboronic acid hydrochloric salt

[1,1':3',1''-terphenyl]-3,3

[1,1':3',1''-terphenyl]-3,3",5'-triamine

Conditions
ConditionsYield
With tetrakis(triphenylphosphine) palladium(0); Aliquat 336; potassium carbonate In tetrahydrofuran at 75℃; for 24h; Reflux; Inert atmosphere;81%
3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

3,5-bis-trifluromethylphenylboronic acid
73852-19-4

3,5-bis-trifluromethylphenylboronic acid

3,3'',5,5''-tetrakis(trifluoromethyl)-[1,1':3',1''-terphenyl]-5'-amine

3,3'',5,5''-tetrakis(trifluoromethyl)-[1,1':3',1''-terphenyl]-5'-amine

Conditions
ConditionsYield
With dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane; palladium diacetate; potassium carbonate In tetrahydrofuran; water Inert atmosphere; Reflux;81%
3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

benzyl bromide
100-39-0

benzyl bromide

N,N-dibenzyl-3,5-dibromoaniline

N,N-dibenzyl-3,5-dibromoaniline

Conditions
ConditionsYield
With potassium carbonate In acetonitrile at 125℃; for 4h;80%
With potassium carbonate In acetonitrile at 125℃; for 4h; Inert atmosphere; Schlenk technique;80%
With potassium carbonate In acetonitrile for 24h; Reflux;73%
With potassium carbonate In acetonitrile Reflux;73%
3,5-dibromoaniline
626-40-4

3,5-dibromoaniline

3-(4-fluorophenyl)-4-hydroxyfuran-2(5H)-one
100074-46-2

3-(4-fluorophenyl)-4-hydroxyfuran-2(5H)-one

4-(3,5-dibromophenylamino)-3-(4-fluorophenyl)furan-2(5H)-one
1283094-23-4

4-(3,5-dibromophenylamino)-3-(4-fluorophenyl)furan-2(5H)-one

Conditions
ConditionsYield
With toluene-4-sulfonic acid In toluene at 90℃; Reflux;79%

626-40-4Relevant articles and documents

A Cu(II)-MOF capable of fixing CO2 from air and showing high capacity H2 and CO2 adsorption

Sharma, Vivekanand,De, Dinesh,Saha, Ranajit,Das, Ranjita,Chattaraj, Pratim Kumar,Bharadwaj, Parimal K.

, p. 13371 - 13374 (2017)

A porous Cu(ii)-MOF shows an adsorption of 6.6 wt% of H2 at 77 K and 62 bar and a very high 60 wt% of CO2 at 298 K and 32 bar. When air is bubbled into a suspension of the activated MOF in the presence of different epoxides at room temperature, the CO2 in air is readily converted into the corresponding cyclic carbonates.

Fe/Fe3C Encapsulated in N-Doped Carbon Tubes: A Recyclable Catalyst for Hydrogenation with High Selectivity

Yun, Ruirui,Zhang, Shi,Ma, Wanjiao,Lv, Xiao,Liu, Shoujie,Sheng, Tian,Wang, Suna

supporting information, p. 9469 - 9475 (2019/08/20)

Herein, a series of Fe-based catalysts have been designed and prepared by grinding a mixture of MIL-88d and melamine, and then the mixture was followed by pyrolysis. An unusual Fe/Fe3C-activated site is uniformly encapsulated in the N-doped carbon tubes obtained by pyrolysis of the film-like nanocrystals of MIL-88d. Experimental characterizations and theoretical calculations demonstrate that the surface N sites can effectively trap the nitrobenzene and aniline by their phenyl groups with the formation of three C-N bonds that made the catalyst exhibit excellent catalytic activity (turnover frequencies of ≤11268 h-1 calculated on the basis of nitrobenzene) and chemoselectivity for the reduction of nitro derivatives under facile conditions.

FHBC, a Hexa-peri-hexabenzocoronene–Fluorene Hybrid: A Platform for Highly Soluble, Easily Functionalizable HBCs with an Expanded Graphitic Core

Navale, Tushar S.,Ivanov, Maxim V.,Hossain, Mohammad M.,Rathore, Rajendra

supporting information, p. 790 - 794 (2017/12/26)

Materials based upon hexa-peri-hexabenzocoronenes (HBCs) show significant promise in a variety of photovoltaic applications. There remains the need, however, for a soluble, versatile, HBC-based platform, which can be tailored by incorporation of electroactive groups or groups that can prompt self-assembly. The synthesis of a HBC–fluorene hybrid is presented that contains an expanded graphitic core that is highly soluble, resists aggregation, and can be readily functionalized at its vertices. This new HBC platform can be tailored to incorporate six electroactive groups at its vertices, as exemplified by a facile synthesis of a representative hexaaryl derivative of FHBC. Synthesis of new FHBC derivatives, containing electroactive functional groups that can allow controlled self-assembly, may serve as potential long-range charge-transfer materials for photovoltaic applications.

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