207518-98-7

Basic information

• Product Name: cis-Cyclohexan-dicarbonsaeure-1,2-monoamid
• Synonyms: cis-Cyclohexan-dicarbonsaeure-1,2-monoamid
• CAS NO: 207518-98-7
• Molecular Weight: 171.196
• Mol File: 207518-98-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: cis-Cyclohexan-dicarbonsaeure-1,2-monoamid(CAS DataBase Reference)
• NIST Chemistry Reference: cis-Cyclohexan-dicarbonsaeure-1,2-monoamid(207518-98-7)
• EPA Substance Registry System: cis-Cyclohexan-dicarbonsaeure-1,2-monoamid(207518-98-7)

Safety Data

• Hazardous Substances Data: 207518-98-7(Hazardous Substances Data)

Upstream product

• 28907-20-2 cis-cyclohexane-1,2-dicarbonitrile 

Relevant articles and documents

Rhodococcus rhodochrous IFO 15564-mediated hydrolysis of alicyclic nitriles and amides: Stereoselectivity and use for kinetic resolution and asymmetrization

The stereocourse and the selectivity of the hydrolysis of alicyclic mono- and dinitriles and amides mediated by Rhodococcus rhodochrous IFO · 15564 has been examined. The stereochemistry of the substrates, as well as the nature of substituents and presence of double bonds in alicyclic rings greatly affected the rate of hydrolysis by nitrile hydratase and amidase. The rate difference between enantiomers or enantiotopic groups, in some cases, enabled kinetic resolution or asymmetrization. The highest enantioselectivity of amidase was observed in the hydrolysis of 5-benzoyloxy-3-cyclohexene-1- carboxamide (E>200), and both enantiomers of methyl 5-hydroxy-3-cyclohexene- 1-carboxylate thus became readily available.