2258-56-2

Basic information

• Product Name: 2-Cyclopentene-1-carboxylic acid methyl ester
• Synonyms: 2-Cyclopentene-1-carboxylic acid methyl ester
• CAS NO: 2258-56-2
• Molecular Formula: C₇H₁₀O₂
• Molecular Weight: 126.15
• Mol File: 2258-56-2.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 149.2±29.0 °C(Predicted)
• Appearance: /
• Density: 1.054±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 2-Cyclopentene-1-carboxylic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Cyclopentene-1-carboxylic acid methyl ester(2258-56-2)
• EPA Substance Registry System: 2-Cyclopentene-1-carboxylic acid methyl ester(2258-56-2)

Safety Data

• Hazardous Substances Data: 2258-56-2(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 201230-82-2 carbon monoxide 
• 142-29-0 cyclopentene 

Downstream Products

• 170423-00-4 methyl cis-2,3-epoxy-1-cyclopentancarboxylate 
• 170423-00-4 methyl trans-2,3-epoxy-1-cyclopentancarboxylate 
• 162086-59-1 3-hydroxy-cyclopentene-1-carboxylic acid methyl ester 
• 101244-89-7 (-)-(1S,2S,6S,7S,8S)-8-benzyloxy-1,5-dimethyltricyclo<5.3.0.0^2,6>dec-4-en-3-one 
• 101244-87-5 (+)-(1S,2S,6S,7S,8S)-8-benzyloxy-3-hydroxymethyl-5-methoxy-1,5-dimethyl-4-oxatricyclo<5.3.0.0^2,6>decane 
• 101244-88-6 (+)-(1S,4S,5S)-6,7-diacetyl-4-benzyloxy-1-methylbicyclo<3.2.0>heptane 
• 101244-86-4 (-)-(1S,5R,8S,9S,10S,13S)-8-benzyloxy-11-methoxy-11-methyl-3,12-dioxatetracyclo<8.2.1.0.^5,90^5,13>tridecan-4-one 
• 101244-83-1 (-)-(1S,5R,8S,9S,10S,13S)-8-benzyloxy-3,12-dioxatetracyclo<8.2.1.0.^5,90^5,13>tridecan-4,11-dione 
• 162086-68-2 (-)-(1R,2S,3S,5R,6R,7S,10R)-5-methoxymethoxy-6,10-dimethyltricyclo<5.3.0.0^2,6>decan-3-yl p-toluenesulfonate 
• 108384-35-6 methyl 3-oxocyclopent-1-enecarboxylate 
• 13668-61-6 (cyclopent-2-eneyl)acetic acid 
• 122278-04-0 α,α-Bis(phenylethynyl)-2-cyclohexene-1-methanol 
• 162086-60-4 methyl 2,3-epoxycyclopentane-1-carboxylate 
• 13668-59-2 3-hydroxymethyl-cyclopentene 

Relevant articles and documents

Oxidative carbomethoxylation of alkenes using a Pd(II)/molybdovanadophosphate (NPMoV) system under carbon monoxide and air

Oxidative carbomethoxylation of cyclopentene (1) under carbon monoxide and air by the use of a catalytic amount of Pd(OAc)2 and molybdovanadophosphate (NPMoV) led to dimethyl cis-1,2-cyclopentanedicarboxylate (2) and dimethyl cis-1,3-cyclopentanedicarboxylate (3) in good yields. Total yields of 2 and 3 were found to be improved by adding a small amount of NH4Cl. Several alkenes were similarly converted into the corresponding dimethyl dicarboxylates. The role of Cl- in the present catalytic system is suggested.