156149-48-3

Basic information

• Product Name: 2-azido-3-methylbenzoic acid
• Synonyms: 2-azido-3-methylbenzoic acid
• CAS NO: 156149-48-3
• Molecular Weight: 177.162
• Mol File: 156149-48-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-azido-3-methylbenzoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-azido-3-methylbenzoic acid(156149-48-3)
• EPA Substance Registry System: 2-azido-3-methylbenzoic acid(156149-48-3)

Safety Data

• Hazardous Substances Data: 156149-48-3(Hazardous Substances Data)

Upstream product

• 108078-14-4 2-iodo-3-methylbenzoic acid 
• 1427465-41-5 1-phenyl-7-methyl-1H-1λ³-benzo[b]iodo-3(2H)-one 
• 1127-59-9 7-methyl-1H-indole-2,3-dione 
• 4389-45-1 3-methylantranilic acid 

Downstream Products

• 428817-09-8 N-(2-azido-3-methyl-benzoyl)-N-benzo[1,3]dioxol-5-ylmethyl-benzamide 
• 428817-19-0 2-azido-3-methylbenzoic acid chloride 
• 156149-49-4 2-azido-3-methylbenzamide 
• 156149-50-7 2-azido-3-methylbenzonitrile 

Relevant articles and documents

Telescoped synthesis of C3-functionalized (E)-arylamidines using Ugi-Mumm and regiospecific quinazolinone rearrangements

An efficient four-step, six-transformation protocol was developed to afford bioactive N-alkyl- or N-arylamide (E)-arylamidines featuring strategic amidine C3 modifications which were inaccessible or low yielding by previous methods. This synthetic approac

Parallel fluorous biphasic synthesis of 3H-quinazolin-4-ones by an Aza-Wittig reaction employing perfluoroalkyl-tagged triphenylphosphine

A perfluoroalkyl-tagged triphenylphosphine was applied in a fluorous biphasic system for the efficient parallel synthesis of 3H-quinazolin-4-ones via an Aza-Wittig reaction. The products were isolated by solid-phase extraction on fluorous reversed-phase silica gel. A new solid-phase bound phosphine derivative was used for comparison and yielded similar results.