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4-Bromo-2-chloroaniline

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4-Bromo-2-chloroaniline manufacturers

4-Bromo-2-chloroaniline Basic information
Product Name:4-Bromo-2-chloroaniline
Synonyms:4-BROMO-2-CHLOROANILINE;4-BROMO-2-CHLOROANILINE, 98+%;4-Bromo-2-chloroanil;4-Bromo-2-chloro-phenylamine;Benzenamine, 4-bromo-2-chloro-;1-Amino-4-bromo-2-chlorobenzene;4-Bromo-2-chloroaniline,99%;4-Bromo-2-chloroanilinev
CAS:38762-41-3
MF:C6H5BrClN
MW:206.47
EINECS:254-118-4
Product Categories:Building Blocks;Chemical Synthesis;Nitrogen Compounds;Organic Building Blocks;C2 to C6;Nitrogen Compounds;Anilines, Aromatic Amines and Nitro Compounds;Benzene series;Anilines, Amides & Amines;Bromine Compounds;Chlorine Compounds;Amines;blocks;Bromides;C6
Mol File:38762-41-3.mol
4-Bromo-2-chloroaniline Structure
4-Bromo-2-chloroaniline Chemical Properties
Melting point 70-72 °C (lit.)
Boiling point 241.8±20.0 °C(Predicted)
density 1.6567 (rough estimate)
refractive index 1.5400 (estimate)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
pka1.95±0.10(Predicted)
form Crystalline Powder
color Slightly yellow to light brown
BRN 3117740
InChIInChI=1S/C6H5BrClN/c7-4-1-2-6(9)5(8)3-4/h1-3H,9H2
InChIKeyINMZDDDQLHKGPF-UHFFFAOYSA-N
SMILESC1(N)=CC=C(Br)C=C1Cl
CAS DataBase Reference38762-41-3(CAS DataBase Reference)
Safety Information
Hazard Codes Xn,T,Xi
Risk Statements 20/21/22-20/21
Safety Statements 36-23
WGK Germany 3
Hazard Note Toxic
HazardClass IRRITANT
HS Code 29214200
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
MSDS Information
ProviderLanguage
4-Bromo-2-chloroaniline English
SigmaAldrich English
ACROS English
ALFA English
4-Bromo-2-chloroaniline Usage And Synthesis
Chemical PropertiesSLIGHTLY YELLOW TO LIGHT BROWN CRYSTALLINE POWDER
Uses4-Bromo-2-chloroaniline was used in the peparation of 3,4-dichloro-α-trichloromethylbenzyl alcohol.
Synthesis
2-Chloroaniline

95-51-2

4-Bromo-2-chloroaniline

38762-41-3

The general procedure for the synthesis of 4-bromo-2-chloroaniline from o-chloroaniline was as follows: 254 mg (2 mmol) of o-chloroaniline and 143 mg (1.2 mmol) of potassium bromide were dissolved in 10 mL of a solvent mixture of acetic acid (AcOH) and water (9:1, v/v), and the solution was subsequently transferred to a 50 mL three-neck flask. The reaction temperature was controlled by magnetic stirring at 25°C for 1 h in a thermostatic water bath with continuous stirring. Within the first 15 min of the start of the reaction, 1.8 g (1.8 mmol) of ZnAl-BrO3-LDHs was slowly added.After completion of the reaction, the reaction mixture was extracted with dichloromethane (2 × 10 mL) and the organic phases were combined. Two silica gels (200-300 mesh) were added to the combined organic phases, and the dichloromethane was subsequently removed by distillation under reduced pressure. Finally, purification was carried out using column chromatography (eluent was a solvent mixture of petroleum ether and ethyl acetate in a 10:1 ratio, v/v) to give 321 mg of gray solid product in 78% yield.

References[1] Tetrahedron Letters, 2005, vol. 46, # 51, p. 8959 - 8963
[2] Russian Journal of Applied Chemistry, 2009, vol. 82, # 9, p. 1570 - 1576
[3] Chinese Chemical Letters, 2012, vol. 23, # 4, p. 387 - 390
[4] Monatshefte fur Chemie, 2013, vol. 144, # 2, p. 179 - 181
[5] Journal of the Iranian Chemical Society, 2012, vol. 9, # 3, p. 321 - 326
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