ChemicalBook--->CAS DataBase List--->46064-79-3

46064-79-3

46064-79-3 Structure

46064-79-3 Structure
IdentificationBack Directory
[Name]

Methyl 3-amino-4-bromobenzoate
[CAS]

46064-79-3
[Synonyms]

Methyl 3-amino-4-bromobenzoate
3-Amino-4-bromo-benzoic acid me
Methyl 3-Amino-4-bromobenzoate 98%
Benzoicacid, 3-aMino-4-broMo-, Methyl ester
benzoic acid,3-amino-4-bromo-,methyl ester,methyl3-amino-4-bromobenzoate,Methyl 3-Amino-4-bromobenzoate,2-bromo-5-methoxycarbonylaniline,3-
[Molecular Formula]

C8H8BrNO2
[MDL Number]

MFCD00553090
[MOL File]

46064-79-3.mol
[Molecular Weight]

230.06
Chemical PropertiesBack Directory
[Melting point ]

118-120°C
[Boiling point ]

337.0±22.0 °C(Predicted)
[density ]

1.578±0.06 g/cm3(Predicted)
[storage temp. ]

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

1.39±0.10(Predicted)
[Appearance]

Off-white to yellow Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H332-H335
[Precautionary statements ]

P261-P280-P305+P351+P338
[HazardClass ]

IRRITANT
[HS Code ]

29163990
Spectrum DetailBack Directory
[Spectrum Detail]

Methyl 3-amino-4-bromobenzoate(46064-79-3)1HNMR
Hazard InformationBack Directory
[Synthesis]

Methanol

67-56-1

3-Amino-4-bromobenzoic acid

2840-29-1

Methyl 3-amino-4-bromobenzoate

46064-79-3

General method: 3-Amino-4-bromobenzoic acid (1 eq.) was dissolved in methanol and cooled to 0°C. The mixture was then heated to 0°C and refluxed for 24 hours. Thionyl chloride (2.5 eq.) was added slowly and the reaction mixture was heated to reflux for 24 hours after completion of the addition. After completion of the reaction, the solvent was removed by evaporation and the residue was neutralized with saturated aqueous NaHCO3 solution. Subsequently, the mixture was extracted with ethyl acetate, the organic layers were combined and dried with anhydrous magnesium sulfate. Finally, the target product, methyl 3-amino-4-bromobenzoate, was purified by column chromatography (hexane/ethyl acetate as eluent).

[References]

[1] European Journal of Medicinal Chemistry, 2014, vol. 76, p. 343 - 351
[2] Journal of Medicinal Chemistry, 2016, vol. 59, # 6, p. 2423 - 2435
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