127322-84-3

Basic information

• Product Name: cis-N-(2-(4-acetamido-4-methylcyclohexyl)propan-2-yl)acetamide
• Synonyms: cis-N-(2-(4-acetamido-4-methylcyclohexyl)propan-2-yl)acetamide
• CAS NO: 127322-84-3
• Molecular Weight: 254.373
• Mol File: 127322-84-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: cis-N-(2-(4-acetamido-4-methylcyclohexyl)propan-2-yl)acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: cis-N-(2-(4-acetamido-4-methylcyclohexyl)propan-2-yl)acetamide(127322-84-3)
• EPA Substance Registry System: cis-N-(2-(4-acetamido-4-methylcyclohexyl)propan-2-yl)acetamide(127322-84-3)

Safety Data

• Hazardous Substances Data: 127322-84-3(Hazardous Substances Data)

Upstream product

• 565-48-0 cis-1,8-terpine 
• 75-05-8 acetonitrile 
• 177698-19-0 Beta-pinene 
• 80-56-8 Pinene 
• 80-53-5 terpin hydrate 

Relevant articles and documents

Skeletal rearrangement in the Ritter reaction of turpentine: A novel synthesis of p-menthane diamides

A novel skeletal rearrangement in the Ritter reaction was examined which conveniently generated p-menthane diamides from turpentine. A probable reaction mechanism was proposed based on employing thermodynamic analysis. All the products were purified and characterised by1H NMR, IR, X-ray crystallography and ESI+-MS.

STEREOSELECTIVE SYNTHESIS OF N,N'-DIACYL-p-MENTHANE-1,8-DIAMINES

It has been shown that the interaction of terpin hydrate with various nitriles under the conditions of the Ritter reaction takes place stereoselectively and leads to the formation of a mixture of isomeric cis- and trans-N,N'-diacyl-p-menthane-1,8-diamines in a ratio of 1:4.The structures of the products have been shown by 1H and 13C spectroscopy.