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ChemicalBook--->CAS DataBase List--->30273-47-3

30273-47-3

30273-47-3 Structure

30273-47-3 Structure
IdentificationBack Directory
[Name]

4-Bromo-5-chloro-2-methylaniline
[CAS]

30273-47-3
[Synonyms]

(4-bromo-5-chloro-2-methylphenyl)amine
BenzenaMine, 4-broMo-5-chloro-2-Methyl-
product NaMe 4-broMo-5-chloro-2-Methylaniline
[Molecular Formula]

C7H7BrClN
[MDL Number]

MFCD07782182
[MOL File]

30273-47-3.mol
[Molecular Weight]

220.49
Chemical PropertiesBack Directory
[Boiling point ]

292.0±35.0 °C(Predicted)
[density ]

1.619±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[pka]

2.69±0.10(Predicted)
[Appearance]

Light brown to brown Solid
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[Hazard Codes ]

Xi
[HazardClass ]

IRRITANT
[HS Code ]

2921490090
Hazard InformationBack Directory
[Uses]

4-Bromo-5-chloro-2-methylaniline can be used as an intermediate in the manufacturing of dyes and pigments, where its chemical structure imparts color and stability to these products.
[Synthesis]

5-Chloro-2-methylaniline

95-79-4

4-Bromo-5-chloro-2-methylaniline

30273-47-3

Example 1A; 4-Bromo-5-chloro-2-methylaniline; 321.6 g (2.01 mol) of bromine was slowly added dropwise to 6000 ml of glacial acetic acid solution containing 300.0 g (2.12 mol) of 5-chloro-2-methylaniline at 10-15 °C. After the dropwise addition, the reaction mixture was stirred at room temperature overnight. After completion of the reaction, the precipitate was separated by filtration and the filtrate was washed with ethyl acetate. Subsequently, the resulting solid was stirred with ethyl acetate and saturated sodium bicarbonate solution to separate the organic phase and the solvent was thoroughly removed using a rotary evaporator. After two recrystallizations from hexane, 186 g (38% yield) of the target product 4-bromo-5-chloro-2-methylaniline was obtained.The results of the LC-MS (Method 1) analysis were: retention time Rt = 2.26 min, and mass-to-charge ratio m/z = 220 ([M + H]+).

[References]

[1] Patent: US2010/105673, 2010, A1. Location in patent: Page/Page column 12
Spectrum DetailBack Directory
[Spectrum Detail]

4-Bromo-5-chloro-2-methylaniline(30273-47-3)1HNMR
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