73873-19-5

Basic information

• Product Name: (1S,2S,4S)-2-Propyl-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid
• Synonyms: (1S,2S,4S)-2-Propyl-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid
• CAS NO: 73873-19-5
• Molecular Weight: 180.247
• Mol File: 73873-19-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (1S,2S,4S)-2-Propyl-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,2S,4S)-2-Propyl-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid(73873-19-5)
• EPA Substance Registry System: (1S,2S,4S)-2-Propyl-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid(73873-19-5)

Safety Data

• Hazardous Substances Data: 73873-19-5(Hazardous Substances Data)

Upstream product

• 934-30-5 5-norbornene-endo-2-carboxylic acid 
• 107-08-4 1-iodo-propane 

Relevant articles and documents

Broadly Applicable Ytterbium-Catalyzed Esterification, Hydrolysis, and Amidation of Imides

An efficient, broadly applicable, operationally simple, and divergent process for the transformation of imides into a range of carboxylic acid derivatives under mild conditions is reported. By simply using catalytic amounts of ytterbium(III) triflate as a Lewis acid promoter in the presence of alcohols, water, amines, or N,O-dimethylhydroxylamine, a broad range of imides is smoothly and readily converted to the corresponding esters, carboxylic acids, amides, and Weinreb amides in good yields. This method notably enables an easy cleavage of oxazolidinone-based auxiliaries.