39880-26-7

Basic information

• Product Name: 2-Cyclohexene-1-carboxylic acid, 2,3-dimethyl-4-oxo-, ethyl ester
• CAS NO: 39880-26-7
• Molecular Formula: C11H16O3
• Molecular Weight: 196.246
• Mol File: 39880-26-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-Cyclohexene-1-carboxylic acid, 2,3-dimethyl-4-oxo-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Cyclohexene-1-carboxylic acid, 2,3-dimethyl-4-oxo-, ethyl ester(39880-26-7)
• EPA Substance Registry System: 2-Cyclohexene-1-carboxylic acid, 2,3-dimethyl-4-oxo-, ethyl ester(39880-26-7)

Safety Data

• Hazardous Substances Data: 39880-26-7(Hazardous Substances Data)

Upstream product

• 487-51-4 4-carbethoxy-3-methyl-2-cyclohexen-1-one 
• 71898-89-0 diethyl 4-hydroxy-4-methyl-6-oxocyclohexane-1,3-dicarboxylate 
• 74-88-4 methyl iodide 
• 74-83-9 methyl bromide 

Downstream Products

• 1551-89-9 trans-2,3-dimethylcyclohexanone 
• 1551-71-9 (+/-)-trans-2,3-dimethyl-cyclohexanone semicarbazone 
• 3883-54-3 2,3-dimethyl-cyclohex-2-enone-(2,4-dinitro-phenylhydrazone) 
• 39880-18-7 1-tert-Butyl-2,3,4-trimethylcyclohex-2-en-1-ol 
• 39880-23-4 4-tert-Butyl-1,2,3-trimethylcyclohexa-1,3-dien 
• 39880-25-6 1-tert-Butyl-2,4-dimethyl-3-methylencyclohex-1-en 
• 39880-24-5 3-tert-Butyl-1,2,6-trimethylcyclohexa-1,3-dien 
• 90768-45-9 2,3-dimethyl-cyclohex-2-enone semicarbazone 
• 222615-12-5 3-(3-diazo-2-oxo-propyl)-2,3-dimethyl-4-methylene-cyclohexanone 
• 200402-94-4 3-(3-Diazo-2-oxo-butyl)-2,3-dimethyl-4-methylene-cyclohexanone 
• 241813-69-4 ethyl 2-(1,2-dimethyl-6-methylene-3-oxocyclohexyl)acetate 
• 200402-93-3 2-(1,2-dimethyl-6-methylene-3-oxocyclohexyl)acetic acid 
• 1122-20-9 2,3-dimethylcyclohex-2-en-1-one 
• 97946-48-0 4-ethoxycarbonyl-2,3-dimethyl-4-(2-phenylsulphinylethyl)-cyclohex-2-enone 

Relevant articles and documents

A formal total synthesis of (±)-homogynolide-B

A formal total synthesis of (±)-homogynolide-B, a sesquiterpene containing an α-spiro-β-methylene-γ-butyrolactone moiety spirofused to a bicyclo[4.3.0]nonane framework, is described. Thus, Hagemann's ester 11 was converted into the allyl alcohol 16 in thr

Stereocontrolled synthesis of (±)-α-pinguisene and (±)-pinguisenol

Total synthesis of (±)-α-pinguisene 1 and (±)-pinguisenol 2, employing an orthoester Claisen rearrangement and an intramolecular diazo ketone cyclopropanation reaction for the stereospecific construction of vicinal quaternary carbon atoms, is described.