| Identification | More | [Name]
Methyl 2-amino-4-bromobenzoate | [CAS]
135484-83-2 | [Synonyms]
2-AMINO-4-BROMOBENZOIC ACID METHYL ESTER
METHYL 2-AMINO-4-BROMOBENZOATE
METHYL 4-BROMO-2-AMINOBENZOATE
Methyl 4-bromoanthranilate
4-Bromo-2-Amino Benzoic Acid Methyl Ester
8031 4-BROMO-2-AMINO BENZOIC ACID METHYL ESTER | [Molecular Formula]
C8H8BrNO2 | [MDL Number]
MFCD07783014 | [Molecular Weight]
230.06 | [MOL File]
135484-83-2.mol |
| Chemical Properties | Back Directory | [Melting point ]
77-79°C | [Boiling point ]
319.3±22.0 °C(Predicted) | [density ]
1.578±0.06 g/cm3(Predicted) | [storage temp. ]
2-8°C(protect from light) | [solubility ]
soluble in Methanol | [form ]
powder to crystal | [pka]
1.33±0.10(Predicted) | [color ]
White to Light yellow to Light orange | [CAS DataBase Reference]
135484-83-2(CAS DataBase Reference) |
| Hazard Information | Back Directory | [Chemical Properties]
off-white powder | [Uses]
Methyl 2-amino-4-bromobenzoate is a chemical intermediate in organic synthesis, producing agrochemicals and dyes. It acts as a building block for synthesising various compounds due to its reactivity and ability to undergo substitution reactions. At the molecular level, Methyl 2-amino-4-bromobenzoate participates in nucleophilic aromatic substitution reactions, where the amino group and the bromine atom play a role in the substitution process. Methyl 2-Amino-4-Bromobenzoate′s mechanism of action involves its participation in forming new chemical bonds, creating more complex molecules with specific structural and functional properties. Methyl 2-amino-4-bromobenzoate is a versatile chemical for constructing diverse chemical structures, contributing to the exploration of new compounds with potential applications in various fields. | [References]
[1] Patent: CN107778229, 2018, A. Location in patent: Paragraph 0026
[2] Patent: WO2006/48727, 2006, A1. Location in patent: Page/Page column 77
[3] Patent: CN103554007, 2016, B. Location in patent: Paragraph 0044; 0052; 0053
[4] British Journal of Pharmacology, 2018, vol. 175, # 12, p. 2504 - 2519
[5] Journal of the Chemical Society, 1931, p. 72,73 |
|
|