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Home > Encyclopedia > 2-Bromo-6-chloro-4-nitroaniline

2-Bromo-6-chloro-4-nitroaniline

2-Bromo-6-chloro-4-nitroaniline structure

2-Bromo-6-chloro-4-nitroaniline 

structure
  • CAS No:

    99-29-6

  • Formula:

    C6H4BrClN2O2

  • Chemical Name:

    2-Bromo-6-chloro-4-nitroaniline

  • Synonyms:

    Benzenamine,2-bromo-6-chloro-4-nitro-;Aniline,2-bromo-6-chloro-4-nitro-;2-Bromo-6-chloro-4-nitrobenzenamine;2-Bromo-6-chloro-4-nitroaniline;2-Bromo-4-nitro-6-chloroaniline;2-Chloro-6-bromo-4-nitroaniline;6-Bromo-2-chloro-4-nitroaniline;NSC 88985;1-Amino-2-bromo-4-nitro-6-chlorobenzene;2-Chloro-4-nitro-6-bromoaniline

  • Categories:

    Organic Chemistry  >  Amides

2-Bromo-6-chloro-4-nitroaniline Basic Attributes

251.47

251.47

2372771

202-745-9

88985

DTXSID2059192

2921420090

Characteristics

71.8

2.4

Pale Yellow Powder

1.9±0.1 g/cm3

177.4 °C

344.7ºC at 760 mmHg

162.3±26.5 °C

1.677

Safety Information

II

6.1

NONH for all modes of transport

3

36/37/38

26-36

Xi

P261-P305 + P351 + P338

H315-H319-H335

|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 43 companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

2-Bromo-6-chloro-4-nitroaniline Use and Manufacturing

Methods of Manufacturing

A solution of 345 mg (2 mmol) of 2-chloro-4-nitroaniline, 143 mg (1.2 mmol) of potassium bromide was added to 50 ml of three neck The flask was then added with 10 ml of AcOH: H2O = 9: 1 solvent and transferred to a constant temperature magnetic stirring water bath. The control temperature wasThe reaction was stirred at 30 ° C for 1 hour, and 1.8 g (1.8 mmol) of ZnAl-BrO3 - LDHs was slowly added in portions 15 minutes before the reaction. anti- After completion, the reaction solution was extracted with dichloromethane, the organic phases were combined, and two syrups were added to the dichloromethane phase to separate the silica gel(200-300 mesh) and the dichloromethane was distilled off under reduced pressure, and the residue was purified by column chromatography (petroleum ether: ethyl acetate = 10: 1 as Eluent) to give a pure product, 478 mg. The material was a yellow solid in 95percent yield.A solution of 345 mg (2 mmol) of 2-chloro-4-nitroaniline, 143 mg (1.2 mmol) of potassium bromide was added to 50 ml of three neck The flask was then added with 10 ml of AcOH: H2O = 9: 1 solvent and transferred to a constant temperature magnetic stirring water bath. The control temperature wasThe reaction was stirred at 30 ° C for 1 hour, and 1.8 g (1.8 mmol) of ZnAl-BrO3 - LDHs was slowly added in portions 15 minutes before the reaction. anti- After completion, the reaction solution was extracted with dichloromethane, the organic phases were combined, and two syrups were added to the dichloromethane phase to separate the silica gel(200-300 mesh) and the dichloromethane was distilled off under reduced pressure, and the residue was purified by column chromatography (petroleum ether: ethyl acetate = 10: 1 as Eluent) to give a pure product, 478 mg. The material was a yellow solid in 95percent yield.

Uses

Used as an intermediate in organic synthesis

Benzenamine, 2-bromo-6-chloro-4-nitro-: ACTIVE

Computed Properties

Molecular Weight:251.46
XLogP3:2.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Exact Mass:249.91447
Monoisotopic Mass:249.91447
Topological Polar Surface Area:71.8
Heavy Atom Count:12
Complexity:187
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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