126972-57-4

Basic information

• Product Name: 1H-Cyclopent[c]isoxazole-1-ethanol,-alpha--ethylhexahydro-,[1(S*),3a-alpha-,6a-alpha-]-(9CI)
• Synonyms: 1H-Cyclopent[c]isoxazole-1-ethanol,-alpha--ethylhexahydro-,[1(S*),3a-alpha-,6a-alpha-]-(9CI)
• CAS NO: 126972-57-4
• Molecular Formula: C10H19NO2
• Molecular Weight: 185.26336
• Product Categories: CYCLOPENTANE
• Mol File: 126972-57-4.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1H-Cyclopent[c]isoxazole-1-ethanol,-alpha--ethylhexahydro-,[1(S*),3a-alpha-,6a-alpha-]-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Cyclopent[c]isoxazole-1-ethanol,-alpha--ethylhexahydro-,[1(S*),3a-alpha-,6a-alpha-]-(9CI)(126972-57-4)
• EPA Substance Registry System: 1H-Cyclopent[c]isoxazole-1-ethanol,-alpha--ethylhexahydro-,[1(S*),3a-alpha-,6a-alpha-]-(9CI)(126972-57-4)

Safety Data

• Hazardous Substances Data: 126972-57-4(Hazardous Substances Data)

Upstream product

• 106-88-7 ethyloxirane 
• 57606-81-2 hex-5-enal oxime 

Relevant articles and documents

TANDEM NUCLEOPHILIC SUBSTITUTION - 1,3 DIPOLAR CYCLOADDITION REACTIONS OF OXIMES WITH EPOXIDES AND DIPOLAROPHILES.

Regiospecific nucleophilic substitution reactions involving attack of the nitrogen atom of oximes on epoxides are used to generate nitrones which are then trapped in 1,3-dipolar cycloaddition reactions.These tandem processes are shown to be flexible and to have wide synthetic scope for the construction of complex molecular frameworks.