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2-Bromo-4-(trifluoromethyl)aniline

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2-Bromo-4-(trifluoromethyl)aniline Basic information

Product Name:
2-Bromo-4-(trifluoromethyl)aniline
Synonyms:
  • 2-Bromo-4-(trifluoromethyl)aniline, 2-Bromo-alpha,alpha,alpha-trifluoro-p-toluidine
  • 4-AMino-3-broMobenzotrifluoride SynonyMs 2-BroMo-4-(trifluoroMethyl)aniline
  • 4-amino-3-bromo-trifluoromethylbenzene
  • Benzenamine,2-bromo-4-(trifluoromethyl)-
  • BUTTPARK 44\03-51
  • TIMTEC-BB SBB000789
  • 2-BROMO-4-TRIFLUOROMETHYL-PHENYLAMINE
  • 2-BROMO-4-(TRIFLUOROMETHYL)ANILINE
CAS:
57946-63-1
MF:
C7H5BrF3N
MW:
240.02
EINECS:
261-035-7
Product Categories:
  • Amines
  • C7
  • Aromatic Halides (substituted)
  • Aniline
  • Benzotrifluoride Series
  • Nitrogen Compounds
Mol File:
57946-63-1.mol
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2-Bromo-4-(trifluoromethyl)aniline Chemical Properties

Melting point:
26-28°C
Boiling point:
109-110 °C10 mm Hg(lit.)
Density 
1,7 g/cm3
refractive index 
n20/D 1.524(lit.)
Flash point:
110 °C
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
form 
Crystals
pka
0.70±0.10(Predicted)
color 
White
BRN 
8139978
CAS DataBase Reference
57946-63-1(CAS DataBase Reference)
NIST Chemistry Reference
Benzenamine, 2-bromo-4-(trifluoromethyl)-(57946-63-1)
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
36/37/38-20/21/22
Safety Statements 
26-36-36/37/39
RIDADR 
2810
WGK Germany 
3
Hazard Note 
Irritant
HazardClass 
6.1
HS Code 
29214990

MSDS

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2-Bromo-4-(trifluoromethyl)aniline Usage And Synthesis

Chemical Properties

white crystals

Uses

2-Bromo-4-(trifluoromethyl)aniline is mainly used as a raw material for organic synthesis or a reagent for chemical reactions, and can be used to prepare 2-Amino-5-trifluoromethylbenzonitrile and 2-Bromo-1-nitro-4-(trifluoromethyl) benzene among other organic heterocyclic compounds.

Synthesis

2-Bromo-4-(trifluoromethyl)aniline is prepared by reacting 4-(trifluoromethyl)aniline with N-bromosuccinimide in dichloromethane. The following is the reaction procedure:
Add 200 mL of distilled CH2Cl 2 and 4- (trifluoromethyl) aniline (20 g, 124.13 mmol) to a two neck flask. Slowly dropwise N-bromosuccinimide (24.3 g, 136.5 mmol) dissolved in CH2Cl2. When the reaction is complete, extract with CH2Cl2. Purification by column separation (EA: Hx = 1: 4) (yield: 50percent)

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