14715-37-8

Basic information

• Product Name: (1S,2S)-2-(carboxymethyl)cyclohexanecarboxylic acid
• CAS NO: 14715-37-8
• Molecular Formula: C₉H₁₄O₄
• Molecular Weight: 186.2051
• Mol File: 14715-37-8.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 398.2°C at 760 mmHg
• Flash Point: 208.8°C
• Density: 1.233g/cm³
• Vapor Pressure: 1.88E-07mmHg at 25°C
• Refractive Index: 1.503
• CAS DataBase Reference: (1S,2S)-2-(carboxymethyl)cyclohexanecarboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,2S)-2-(carboxymethyl)cyclohexanecarboxylic acid(14715-37-8)
• EPA Substance Registry System: (1S,2S)-2-(carboxymethyl)cyclohexanecarboxylic acid(14715-37-8)

Safety Data

• Hazardous Substances Data: 14715-37-8(Hazardous Substances Data)

Upstream product

• 10479-70-6 (+/-)-(cis-2-carboxy-cyclohexyl)-acetic acid 
• 10479-70-6 (+/-)-(trans-2-carboxy-cyclohexyl)-acetic acid 
• 89-51-0 Homophthalic acid 
• 96308-39-3 cis-(3aα,7aα)-3a,4,5,6,7,7a-hexahydro-1H-indene 
• 68429-52-7 hexahydro-naphthalene-1,3-dione 
• 716-43-8 dimethyl homophthalate 
• 10479-84-2 (E)-Pent-2-endinitril 
• 1617-22-7 cyclohex-1-enecarboxylic acid ethyl ester 
• 98202-45-0 ethyl (2E)-7-iodohept-2-enoate 
• 98202-47-2 (1S,2R)-2-tert-Butoxycarbonylmethyl-cyclohexanecarboxylic acid ethyl ester 
• 2743-89-7 (+/-)-(trans-6-carboxy-cyclohex-3-enyl)-acetic acid 
• 81143-96-6 (2-ethoxycarbonyl-cyclohexyl)-malonic acid diethyl ester 
• 859819-96-8 (2-carboxy-cyclohexyl)-malonic acid 
• 16484-17-6 trans-octahydro-2H-inden-2-one 

Downstream Products

• 10479-70-6 (+)-(trans-2-carboxy-cyclohexyl)-acetic acid 
• 10479-70-6 (-)-(trans-2-carboxy-cyclohexyl)-acetic acid 
• 10479-70-6 (+)-(cis-2-carboxy-cyclohexyl)-acetic acid 
• 10479-70-6 (-)-(cis-2-carboxy-cyclohexyl)-acetic acid 
• 24112-71-8 cis-2-(hydroxymethylcyclohexyl)ethanol 

Relevant articles and documents

The Stereochemistry of Organometallic Compounds. XXXVIII. Regio- and Stereo-control in the Rhodium-Catalysed Hydroformylation of Some Alkenyl Phosphites

Excellent regiocontrol is achieved in the rhodium-catalysed hydroformylation of some alkenyl phosphites, and good stereocontrol is obtained in the hydroformylation of some cyclohexenyl phosphites.The stereochemical results have implications for the mechanism of these rhodium-catalysed reactions.