2-Bromo-6-chloro-4-nitroaniline
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2-Bromo-6-chloro-4-nitroaniline
structure -
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CAS No:
99-29-6
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Formula:
C6H4BrClN2O2
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Chemical Name:
2-Bromo-6-chloro-4-nitroaniline
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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
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CAS No:
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
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.
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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