31928-20-8

Basic information

• Product Name: methyl 2-amino-3,4-dimethylbenzoate
• Synonyms: methyl 2-amino-3,4-dimethylbenzoate
• CAS NO: 31928-20-8
• Molecular Weight: 179.219
• Mol File: 31928-20-8.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: methyl 2-amino-3,4-dimethylbenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 2-amino-3,4-dimethylbenzoate(31928-20-8)
• EPA Substance Registry System: methyl 2-amino-3,4-dimethylbenzoate(31928-20-8)

Safety Data

• Hazardous Substances Data: 31928-20-8(Hazardous Substances Data)

Upstream product

• 91061-57-3 methyl 2-hydroxy-3,4-dimethylbenzoate 
• 50419-58-4 2-amino-3,4-dimethylbenzoic acid 
• 74-88-4 methyl iodide 
• 67-56-1 methanol 

Relevant articles and documents

INDAZOLE DERIVATIVES AS INHIBITORS OF SARM1

The present disclosure provides compounds of formula (I) and methods useful for inhibiting SARM1 and/or treating and/or preventing axonal degeneration.

A Potent and Selective PARP11 Inhibitor Suggests Coupling between Cellular Localization and Catalytic Activity

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Asymmetric Synthesis of Fused Polycyclic Indazoles through Aminocatalyzed Aza-Michael Addition/Intramolecular Cyclization

The first example of an asymmetric aminocatalyzed aza-Michael addition of 1H-indazole derivatives to α,β-unsaturated aldehydes is described. The iminium/enamine cascade process lies at the heart of our strategy, leading to enantioenriched fused polycyclic indazole architectures. Variations on both the α,β-unsaturated aldehydes and the indazole-7-carbaldehyde heterocycles were studied in order to broaden the scope of the transformation in synthetically interesting directions. The fused polycyclic indazoles exhibit fluorescence properties and can undergo synthetic transformations.