55289-36-6
Chemical Structure
3-Bromo-2-methylaniline
- CAS No.: 55289-36-6
- Formula:C7H8BrN
- Molecular Weight:186.05
IUPAC Name: 3-bromo-2-methylaniline
InChIKey: IILVSKMKMOJHMA-UHFFFAOYSA-N
SMILES: NC1=CC=CC(Br)=C1C
Biological Activity: 3-Bromo-2-methylaniline is an aromatic amine compound and aniline derivative that serves as a starting material and synthetic precursor. 3-Bromo-2-methylaniline acts as a starting material for the synthesis of 4-bromo-1H-indazole and racemic 3,9-dibromo-4,10-dimethyl-6H,12H-5,11-methanodibenzodiazocine. It also serves as a precursor for the regioselective bromination and subsequent deamination to synthesize 1,2-dibromo-3-methylbenzene[1][2][3].
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3-Bromo-2-methylaniline | 99.81% | 3-Bromo-2-methylaniline is an aromatic amine compound and aniline derivative that serves as a starting material and synthetic precursor. 3-Bromo-2-methylaniline acts as a starting material for the synthesis of 4-bromo-1H-indazole and racemic 3,9-dibromo-4,10-dimethyl-6H,12H-5,11-methanodibenzodiazocine. It also serves as a precursor for the regioselective bromination and subsequent deamination to synthesize 1,2-dibromo-3-methylbenzene. | ||||||||||||||||||||
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- [1]. Qingping Tian, et al. A Practical Synthesis of a PI3K Inhibitor under Noncryogenic Conditions via Functionalization of a Lithium Triarylmagnesiate Intermediate. Org. Process Res. Dev. 2013, 17, 1, 97-107.
- [2]. Kiehne U, et al. Synthesis, resolution, and absolute configuration of difunctionalized Tröger's base derivatives. Chemistry. 2008;14(14):4246-4255. [Content Brief]
- [3]. Vincent Diemer, et al. Efficient and Complementary Methods Offering Access to Synthetically Valuable 1,2-Dibromobenzenes. Eur. J. Org. Chem. 2011, 327-340.
Keywords
