58093-61-1

Basic information

• Product Name: Benzoyl chloride, 2,3,6-trimethoxy-
• CAS NO: 58093-61-1
• Molecular Formula: C10H11ClO4
• Molecular Weight: 230.648
• Mol File: 58093-61-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzoyl chloride, 2,3,6-trimethoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoyl chloride, 2,3,6-trimethoxy-(58093-61-1)
• EPA Substance Registry System: Benzoyl chloride, 2,3,6-trimethoxy-(58093-61-1)

Safety Data

• Hazardous Substances Data: 58093-61-1(Hazardous Substances Data)

Upstream product

• 13909-60-9 1-(2,3,6-trimethoxy-phenyl)-ethanone 
• 135-77-3 1,2,4-trimethoxy-benzene 
• 60241-74-9 2,3,6-trimethoxybenzoic acid 

Downstream Products

• 1354708-15-8 1-(4'-decyl-2'-hydroxyphenyl)-2-methoxy-3-(2'',3'',6''-trimethoxyphenyl)propane-1,3-dione 
• 1354708-08-9 7-decyl-3,2',3',6'-tetrahydroxyflavone 
• 1354708-24-9 7-decyl-3,2',3',6'-tetramethoxyflavone 
• 101460-64-4 (S)-(-)-N-[(1-Ethyl-2-pyrrolidinyl)methyl]-2-hydroxy-5,6-dimethoxybenzamide 
• 98601-22-0 N-((S)-1-Ethyl-pyrrolidin-2-ylmethyl)-2-hydroxy-3,6-dimethoxy-benzamide 
• 476-33-5 (+/-)-homochelidonine 
• 28342-33-8 oxychelerythrine 
• 65341-21-1 N-(3,4-dihydro-6,7-methylenedioxy-1-naphthyl)-2,3,6-trimethoxy-N-methylbenzamide 
• 101460-26-8 N-((S)-1-Ethyl-pyrrolidin-2-ylmethyl)-2,3,6-trimethoxy-benzamide 
• 109092-84-4 2-Hydroxy-2',3,5',6-tetramethoxybenzophenon 

Relevant articles and documents

Synthesis of polyhydroxylated flavonoids bearing a lipophilic decyl tail as potential therapeutic antioxidants

Antioxidants have potential for the treatment of stroke and neurodegeneration, and chimeric compounds that combine a flavon-3-ol head group related to myricetin and a lipophilic decyl tail are known to protect membranes from oxidative damage at least as well as vitamin E. New flavon-3-ols that are highly hydroxylated in the B ring in ways not found in natural flavon-3-ols and bearing a lipophilic decyl tail have been prepared from trimethoxy-and tetramethoxybenzoic acids accessed by lithiation-carboxylation reactions. Direct enolate acylation was preferred over Baker-Venkataraman rearrangement when there were methoxy groups at both the 2-and the 6-position of the benzoic acid derivatives.

Quantitative structure-activity relations of polyhydroxyxanthones, II: Synthesis of polyoxygenated 2-hydroxyxanthones

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