| Identification | More | [Name]
4-Amino-3-bromobenzotrifluoride | [CAS]
57946-63-1 | [Synonyms]
2-BROMO-4-(TRIFLUOROMETHYL)ANILINE
2-BROMO-4-TRIFLUOROMETHYL-PHENYLAMINE
3-BROMO-4-AMINO BENZOTRIFLUORIDE
4-AMINO-3-BROMOBENZOTRIFLUORIDE
BUTTPARK 44\03-51
TIMTEC-BB SBB000789
4-Amino-3-bromobenzotrifluoride,95% (2_Bromo-4-trifluoromethylaniline)
4-Amino-3-bromobenzotrifluoride 98%
4-Amino-3-bromobenzotrifluoride98%
2-Bromo-4-trifluoromethylbenzenamine
4-(Trifluoromethyl)-2-bromoaniline | [EINECS(EC#)]
261-035-7 | [Molecular Formula]
C7H5BrF3N | [MDL Number]
MFCD00042150 | [Molecular Weight]
240.02 | [MOL File]
57946-63-1.mol |
| Safety Data | Back Directory | [Hazard Codes ]
Xi,Xn | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin .
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . | [RIDADR ]
2810 | [WGK Germany ]
3
| [Hazard Note ]
Irritant | [HazardClass ]
6.1 | [HazardClass ]
IRRITANT | [HS Code ]
29214990 | [Storage Class]
10 - Combustible liquids | [Hazard Classifications]
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3 |
| Hazard Information | Back Directory | [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)
 | [References]
[1] Journal of Organic Chemistry, 2018, vol. 83, # 2, p. 930 - 938
[2] Patent: KR2018/50795, 2018, A. Location in patent: Paragraph 0086; 0087; 0104-0106
[3] Patent: US3946025, 1976, A
[4] Chinese Journal of Chemistry, 2018, vol. 36, # 9, p. 815 - 818
[5] Patent: US3995042, 1976, A |
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