125783-07-5

Basic information

• Product Name: (E)-2-cyclohexyl-3-phenylacrylic acid
• Synonyms: (E)-2-cyclohexyl-3-phenylacrylic acid
• CAS NO: 125783-07-5
• Molecular Weight: 230.307
• Mol File: 125783-07-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (E)-2-cyclohexyl-3-phenylacrylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-2-cyclohexyl-3-phenylacrylic acid(125783-07-5)
• EPA Substance Registry System: (E)-2-cyclohexyl-3-phenylacrylic acid(125783-07-5)

Safety Data

• Hazardous Substances Data: 125783-07-5(Hazardous Substances Data)

Upstream product

• 104875-64-1 2-cyclohexyl-1-(triisopropylsiloxy)ethyne 
• 100-52-7 benzaldehyde 
• 3289-28-9 ethyl cyclohexanecarboxylate 
• 210752-61-7 Dibromo-cyclohexyl-acetic acid ethyl ester 
• 42716-73-4 ethyl 2-bromo-2-cyclohexylacetate 
• 124-38-9 carbon dioxide 
• 33414-83-4 1-(2-cyclohexylethynyl)benzene 

Relevant articles and documents

A highly stereoselective synthesis of tri- and tetrasubstituted olefins via ynolates

A highly stereoselective synthesis of tri- and tetrasubstituted olefins has been accomplished by the reactions of ynolates with aldehydes and ketones.

Highly E-selective synthesis of α,β-unsaturated amides from N-2- methoxyphenyl aldimines via lithium ynolates

Lithium ynolates reacted with N-2-methoxyphenyl (OMP) aldimines to afford α,β-unsaturated amides in excellent E-selectivity via a retro- Mannich reaction of the 2:1 adducts (β-lactams), followed by cleavage of the β-lactam enolates. (C) 2000 Elsevier Science Ltd.