77837-68-4

Basic information

• Product Name: Benzoic acid, 4-(2-methyl-3-oxo-1-propenyl)-, ethyl ester, (E)-
• CAS NO: 77837-68-4
• Molecular Formula: C13H14O3
• Molecular Weight: 218.252
• Mol File: 77837-68-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 4-(2-methyl-3-oxo-1-propenyl)-, ethyl ester, (E)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 4-(2-methyl-3-oxo-1-propenyl)-, ethyl ester, (E)-(77837-68-4)
• EPA Substance Registry System: Benzoic acid, 4-(2-methyl-3-oxo-1-propenyl)-, ethyl ester, (E)-(77837-68-4)

Safety Data

• Hazardous Substances Data: 77837-68-4(Hazardous Substances Data)

Upstream product

• 6287-86-1 p-ethoxycarbonylbenzaldehyde 
• 123-38-6 propionaldehyde 
• 77837-66-2 1-(4-carboethoxyphenyl)-2-methyl-1-propene 
• 4696-26-8 (E)-1-ethoxyprop-1-ene 
• 35848-99-8 4-(ethoxycarbonyl)benzaldehyde diethylacetal 

Downstream Products

• 77837-57-1 (1E,3E)-1-(4-carboethoxyphenyl)-2-methyl-4-(1,2-epoxy-2,6,6-trimethylcyclohex-1-yl)-1,3-butadiene 
• 93495-41-1 p-(2,6,10-trimethylundecyl)benzoic acid 
• 944838-35-1 4-(2,6,10-Trimethyl-undecyl)-benzoyl chloride 
• 168984-15-4 4-((1E,3E)-2,6-Dimethyl-hepta-1,3-dienyl)-benzoic acid 
• 93495-42-2 p-(2,6-dimethylheptyl)benzoic acid 
• 161695-17-6 4-(2,6,10-trimethyl-1,3,5,9-undecatetraenyl)benzoic acid 
• 161695-18-7 ethyl p-(2,6,10-trimethyl-1,3,5,9-undecatetraenyl)-benzoate 
• 168984-14-3 4-((1E,3E)-2,6-Dimethyl-hepta-1,3-dienyl)-benzoic acid ethyl ester 
• 77837-56-0 (E)-1-(4-carbethoxyphenyl)-2-methyl-4-(2,6,6-trimethyl-1-cyclohexen-1-yl)butadiene 

Relevant articles and documents

The synthesis of 4-(2,6,10-trimethyl-1,3,5,9-undecatetraenyl)benzoic acid based on alkoxy alkene-acetal condensation

4-(2,6,10-Trimethyl-1,3,5,9-undecatetraenyl)benzoic acid (1) was synthesized starting from ethyl 4-formylbenzoate (2) and linalool.The key intermediate, ethyl 4-(2-methyl-3-oxo-1-propenyl)benzoate (5), was obtained by the addition of diethyl acetal (3), p

Aromatic retinoic acid analogues. Synthesis and pharmacological activity

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