ChemicalBook--->CAS DataBase List--->102169-99-3

102169-99-3

102169-99-3 Structure

102169-99-3 Structure
IdentificationBack Directory
[Name]

2-broMo-4-Methyl-5-nitrobenzenaMine
[CAS]

102169-99-3
[Synonyms]

2-broMo-4-Methyl-5-nitrobenzenaMine
2-BroMo-4-Methyl-5-nitro-phenylaMine
BenzenaMine, 2-broMo-4-Methyl-5-nitro-
[Molecular Formula]

C7H7BrN2O2
[MDL Number]

MFCD01239994
[MOL File]

102169-99-3.mol
[Molecular Weight]

231.05
Chemical PropertiesBack Directory
[Melting point ]

119-120 °C(Solv: ethyl acetate (141-78-6); hexane (110-54-3))
[Boiling point ]

336.8±37.0 °C(Predicted)
[density ]

1.698±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[pka]

0.98±0.10(Predicted)
[Appearance]

Brown to dark brown Solid
Safety DataBack Directory
[HS Code ]

2921490090
Spectrum DetailBack Directory
[Spectrum Detail]

2-broMo-4-Methyl-5-nitrobenzenaMine(102169-99-3)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-Bromo-4-methylaniline

583-68-6

2-broMo-4-Methyl-5-nitrobenzenaMine

102169-99-3

General procedure for the synthesis of 2-bromo-4-methyl-5-nitroaniline using 2-bromo-4-methylaniline as starting material: first, 2-bromo-4-methylaniline (23.8 g) was completely dissolved in concentrated sulfuric acid (119 mL). Subsequently, urea nitrate (15 g) was added slowly and in small batches at a temperature maintained at 10 °C or lower. After addition, the reaction mixture was stirred continuously at 0°C for 10 minutes. Upon completion of the reaction, water (120 mL) and 5 M aqueous sodium hydroxide (205 mL) were sequentially added to the reaction solution to neutralize the reaction system. Finally, the precipitated solid product was collected by filtration to afford the target compound 2-bromo-4-methyl-5-nitroaniline (26.3 g).

[References]

[1] European Journal of Organic Chemistry, 2009, # 5, p. 687 - 698
[2] Journal of the American Chemical Society, 1950, vol. 72, p. 2971
[3] Kogyo Kagaku Zasshi, 1956, vol. 59, p. 1093
[4] Chem.Abstr., 1958, p. 11779
[5] Journal of the American Chemical Society, 1950, vol. 72, p. 2971
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