121639-09-6

Basic information

• Product Name: N-(2,3-DIMETHOXYPHENYL)ACETAMIDE
• Synonyms: N-(2,3-DIMETHOXYPHENYL)ACETAMIDE
• CAS NO: 121639-09-6
• Molecular Formula: C₁₀H₁₃NO₃
• Molecular Weight: 195.22
• Mol File: 121639-09-6.mol

Chemical Properties

• Melting Point: 81-83°C
• Appearance: /
• CAS DataBase Reference: N-(2,3-DIMETHOXYPHENYL)ACETAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2,3-DIMETHOXYPHENYL)ACETAMIDE(121639-09-6)
• EPA Substance Registry System: N-(2,3-DIMETHOXYPHENYL)ACETAMIDE(121639-09-6)

Safety Data

• Hazardous Substances Data: 121639-09-6(Hazardous Substances Data)

Upstream product

• 6299-67-8 2,3-dimethoxyaniline 
• 75-36-5 acetyl chloride 
• 1521-38-6 2,3-dimethoxybenzoic acid 
• 56475-31-1 2.3-Dimethoxybenzoylazid 
• 7169-06-4 2,3-dimethoxybenzoyl chloride 

Downstream Products

• 198994-79-5 N-(2',3'-dimethoxyphenyl)-4-bromo-2,5-dimethylacetanilide 
• 93525-21-4 2,3-dihydroxyacetanilide 
• 198994-80-8 N-(2',3'-dimethoxyphenyl)-4-bromo-2,5-dimethylaniline 
• 104778-03-2 (2,3-Dimethoxy-phenyl)-(2-methoxy-4-methyl-phenyl)-amine 
• 861298-61-5 4-bromo-2,3-dimethoxy-aniline 
• 7461-55-4 3-bromo-5-nitrocatechol dimethyl ether 
• 5424-43-1 3-bromoveratrole 
• 861797-65-1 acetic acid-(2,3-dimethoxy-4,5-dinitro-anilide) 
• 861797-87-7 acetic acid-(4-bromo-2,3-dimethoxy-anilide) 
• 861793-39-7 2,3-dimethoxy-5,6-dinitro-aniline 

Relevant articles and documents

Aerobic oxidative homocoupling reaction of anilides using heterogeneous metal catalysts

We have developed a heterogeneous catalytic oxidative homocoupling reaction of dimethoxyanilides under an oxygen atmosphere. The resulting homo-dimers are useful for the construction of heterocycles, demonstrating the potential of heterogeneous metal catalysts.

Acetamidoquinone and acetamidohydroxy derivatives as inhibitors for both dihydroxyacetamido epoxidase and dehydrogenase

A series of monohydroxy and dihydroxyacetanilides, acetamidoquinones and bromoacetamidoquinones have been synthesised and tested as substrates and/or inhibitors of highly purified dihydroxyacetamido epoxidase (DHAE) and dihydroxy acetamido dehydrogenase (DHADH) from Streptomyces LL-C10337. None was found to act as substrates but many selectively inhibit the enzymes. Kinetic analysis has shown that all the compounds act as reversible competitive inhibitors with respect to the substrates 2,5-dihydroxyacetanilide and 2,3-epoxy-1,4-benzoquinone-5-acetanilide. Monohydroxy acetanilides showed weak inhibition to these enzymes compared to the dihydroxy derivatives while the more powerful inhibitors were the benzoquinoneacetanilide and its 5-bromo equivalent.