293731-03-0

Basic information

• Product Name: (3,4-dimethoxy-2-methyl-phenyl)-oxo-acetic acid ethyl ester
• Synonyms: (3,4-dimethoxy-2-methyl-phenyl)-oxo-acetic acid ethyl ester
• CAS NO: 293731-03-0
• Molecular Weight: 252.267
• Mol File: 293731-03-0.mol

Chemical Properties

• CAS DataBase Reference: (3,4-dimethoxy-2-methyl-phenyl)-oxo-acetic acid ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (3,4-dimethoxy-2-methyl-phenyl)-oxo-acetic acid ethyl ester(293731-03-0)
• EPA Substance Registry System: (3,4-dimethoxy-2-methyl-phenyl)-oxo-acetic acid ethyl ester(293731-03-0)

Safety Data

• Hazardous Substances Data: 293731-03-0(Hazardous Substances Data)

Upstream product

• 4463-33-6 1,2-dimethoxy-3-methylbenzene 
• 4755-77-5 Ethyl oxalyl chloride 
• 338446-32-5 [(2,2-dimethoxy-ethyl)-(toluene-4-sulfonyl)-amino]-(3,4-dimethoxy-2-methyl-phenyl)-acetic acid ethyl ester 
• 338446-31-4 (2,2-dimethoxy-ethylamino)-(3,4-dimethoxy-2-methyl-phenyl)-acetic acid ethyl ester 

Downstream Products

• 338446-31-4 (2,2-dimethoxy-ethylamino)-(3,4-dimethoxy-2-methyl-phenyl)-acetic acid ethyl ester 
• 5722-94-1 2-methyl-3,4-dimethoxybenzoic acid 
• 293731-05-2 ethyl (2-acetoxymethyl-3,4-dimethoxyphenyl)-N-[(2,2-dimethoxyethyl)-N-(4-toluenesulfonyl)amino]acetate 
• 338446-32-5 [(2,2-dimethoxy-ethyl)-(toluene-4-sulfonyl)-amino]-(3,4-dimethoxy-2-methyl-phenyl)-acetic acid ethyl ester 
• 338446-36-9 (2-acetoxymethyl-3,4-dimethoxy-phenyl)-(2,2-dimethoxy-ethylamino)-acetic acid ethyl ester 
• 338446-34-7 (2-bromomethyl-3,4-dimethoxy-phenyl)-oxo-acetic acid ethyl ester 

Relevant articles and documents

A practical synthesis of 3,4-dimethoxy-o-toluic acid

A streamlined, telescoped process has been developed for the preparation of 3,4-dimethoxy-o-toluic acid, starting with economical and readily available 2,3-dimethoxybenzaldehyde. Catalytic reduction of the aldehyde functional group generated dimethoxytolu

Synthesis of 4-Hydroxy-7,8-dimethoxyisochroman-3-one and Its Plant Growth-Regulating Properties on Tobacco (Nicotiana tabacum cv. Petit Havana)

The synthesis of 6,7-dimethoxy-4-hydroxyisochroman-3-one 10 from 2,3-dimethoxytoluene (11) via glyoxylate 12 is reported. Compound 10 strongly inhibited vegetative growth of tobacco plants, whereas developmental patterns (protein levels, protein profile, pigments, and chlorophylls) were not affected. Morphological changes were observed in the leaves of the treated plants.

Sulfonamidoacetal cyclization-based synthesis of a tetrahydrooxazaphenalenelactone related to the ABC-ring system of the stephaoxocanes

The elaboration of a tetrahydrooxazaphenalenelactone embodying the ABC-ring system of the stephaoxocanes, by means of Jackson's sulfonamidoacetal cyclization as the isoquinoline ring-forming strategy, is reported.