71195-27-2

Basic information

• Product Name: 2-Cyclohexene-1,4-dicarboxylic acid, dimethyl ester, cis-
• CAS NO: 71195-27-2
• Molecular Formula: C10H14O4
• Molecular Weight: 198.219
• Mol File: 71195-27-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-Cyclohexene-1,4-dicarboxylic acid, dimethyl ester, cis-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Cyclohexene-1,4-dicarboxylic acid, dimethyl ester, cis-(71195-27-2)
• EPA Substance Registry System: 2-Cyclohexene-1,4-dicarboxylic acid, dimethyl ester, cis-(71195-27-2)

Safety Data

• Hazardous Substances Data: 71195-27-2(Hazardous Substances Data)

Upstream product

• 1165952-91-9 cyclohexa-1,3-diene 
• 19618-93-0 2-cyclohexene-1,4-dicarboxylic acid 
• 18107-18-1 diazomethyl-trimethyl-silane 
• 100-21-0 terephthalic acid 
• 186581-53-3 diazomethane 
• 3919-11-7 trans-Cyclohex-2-ene-1,4-dicarboxylic acid 
• 67-56-1 methanol 
• 201230-82-2 carbon monoxide 
• 3919-11-7 cis-Cyclohex-2-ene-1,4-dicarboxylic acid 
• 74-88-4 methyl iodide 

Downstream Products

• 619-81-8 cis-cyclohexane-1,4-dicarboxylic acid 
• 3919-11-7 cis-Cyclohex-2-ene-1,4-dicarboxylic acid 
• 619-82-9 trans-hexahydroterephthalic acid 
• 3919-11-7 trans-Cyclohex-2-ene-1,4-dicarboxylic acid 
• 131721-14-7 (Z)-6-[(1R,4R)-((1Z,4Z)-4-Deca-1,4-dienyl)-cyclohex-2-enyl]-hex-5-enoic acid 
• 131721-16-9 (Z)-5-[(1R,4R)-((1Z,4Z)-4-Deca-1,4-dienyl)-cyclohex-2-enyl]-pent-4-enoic acid 
• 131721-15-8 (5Z,8Z)-9-[(1R,4R)-((Z)-4-Hept-1-enyl)-cyclohex-2-enyl]-nona-5,8-dienoic acid 
• 131721-10-3 2-[(1S,4R)-((1Z,4Z)-4-Deca-1,4-dienyl)-cyclohex-2-enylmethoxy]-tetrahydro-pyran 
• 131721-17-0 (4Z,7Z)-8-[(1R,4R)-((Z)-4-Hept-1-enyl)-cyclohex-2-enyl]-octa-4,7-dienoic acid 
• 131721-11-4 2-[(1S,4R)-((Z)-4-Hept-1-enyl)-cyclohex-2-enylmethoxy]-tetrahydro-pyran 
• 131721-08-9 [(1S,4S)-4-(Tetrahydro-pyran-2-yloxymethyl)-cyclohex-2-enyl]-methanol 

Relevant articles and documents

Ni-Catalyzed Site-Selective Dicarboxylation of 1,3-Dienes with CO2

A site-selective catalytic incorporation of multiple CO2 molecules into 1,3-dienes en route to adipic acids is described. This protocol is characterized by its mild conditions, excellent chemo- and regioselectivity and ease of execution under CO2 (1 atm), including the use of bulk butadiene and/or isoprene feedstocks.