122333-93-1

Basic information

• Product Name: 3-(3,5-dimethoxyphenyl)-2-methylpropenoic acid
• Synonyms: 3-(3,5-dimethoxyphenyl)-2-methylpropenoic acid
• CAS NO: 122333-93-1
• Molecular Weight: 222.241
• Mol File: 122333-93-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3-(3,5-dimethoxyphenyl)-2-methylpropenoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(3,5-dimethoxyphenyl)-2-methylpropenoic acid(122333-93-1)
• EPA Substance Registry System: 3-(3,5-dimethoxyphenyl)-2-methylpropenoic acid(122333-93-1)

Safety Data

• Hazardous Substances Data: 122333-93-1(Hazardous Substances Data)

Upstream product

• 3699-66-9 ethyl 2-diethoxyphosphorylpropionate 
• 7311-34-4 3,5-dimethoxybenzaldehdye 
• 123-62-6 propionic acid anhydride 
• 137-40-6 sodium proprionate 

Downstream Products

• 905920-19-6 2S-methyl-(3,5-dihydroxyphenyl)pentane 
• 187140-42-7 (R)-1-(3,5-dimethoxyphenyl)-2-methylpentane 
• 187140-43-8 (S)-1-(3,5-dimethoxyphenyl)-2-methylpentane 
• 187084-05-5 (S)-2-methyl-3-(3,5-dimethoxyphenyl)-1-propanol 
• 187083-95-0 (R)-2-methyl-3-(3,5-dimethoxyphenyl)-1-propanol 
• 187084-06-6 (S)-3-(3,5-Dimethoxy-phenyl)-2-methyl-propionic acid 
• 187083-96-1 (R)-3-(3,5-dimethoxyphenyl)-2-methylpropionic acid 
• 187084-20-4 N-((1S)-1-phenylethyl)-(2S)-3-(3,5-dimethoxyphenyl)-2-methylpropanamide 
• 187084-19-1 N-((1S)-1-phenylethyl)-(2R)-3-(3,5-dimethoxyphenyl)-2-methylpropanamide 
• 75018-77-8 (S)-3-(3,5-dimethoxyphenyl)-2-methyl-1-propanol tosylate 
• 19314-92-2 3,4-dihydro-6,8-dihydroxy-3-methylisochromen-1-one 
• 61227-52-9 5,7-dimethoxy-2-methylindan-1-one 
• 1204-37-1 saccharonol A 
• 187083-81-4 Toluene-4-sulfonic acid 3-(3,5-dimethoxy-phenyl)-2-methyl-propyl ester 

Relevant articles and documents

Side chain methyl analogues of Δ8-THC

The synthesis of both side chain epimers of 1'- (4), 2'- (5), 3'-methyl- (6) and 4'-methyl-Δ8-tetrahydrocannobinol (7) has been carried out. The synthetic approach entailed the acid catalyzed condensation of the appropriate substituted resorcinol with menthadienol to provide the Δ8-THC analogue. Both isomers of 1'- (4) and 2'-Δ8-THC (5) were more potent than Δ8-THC, both in vitro and in vivo. The 3'-methyl isomers (6) were approximately equal in potency to Δ8-THC, and 4'-methyl-Δ8-THC was less potent. There was relatively little difference in potency between the epimers of 4, 5, and 6.

An Improved Synthesis of 6,8-Dimethoxy-3-methylisocoumarin, a Fungal Metabolite Precursor

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