76059-98-8

Basic information

• Product Name: 1-isoxazolidin-2-ylcyclohexene
• Synonyms: 1-isoxazolidin-2-ylcyclohexene
• CAS NO: 76059-98-8
• Molecular Weight: 153.224
• Mol File: 76059-98-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-isoxazolidin-2-ylcyclohexene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-isoxazolidin-2-ylcyclohexene(76059-98-8)
• EPA Substance Registry System: 1-isoxazolidin-2-ylcyclohexene(76059-98-8)

Safety Data

• Hazardous Substances Data: 76059-98-8(Hazardous Substances Data)

Upstream product

• 504-72-3 isoxazolidine 
• 108-94-1 cyclohexanone 

Downstream Products

• 37087-68-6 2-(4-methoxyphenyl)cyclohexanone 
• 4423-94-3 2-ethylcyclohexanone 
• 1268834-04-3 3-(1-allyl-2-ethylcyclohexylamino)propan-1-ol 
• 4668-64-8 2-(2-methylpropyl)cyclohexanone 
• 52776-14-4 2-(4-methylphenyl)cyclohexanone 
• 1444-65-1 (RS)-2-phenylcyclohexanone 
• 4594-78-9 cyclohexanone-2-propionitrile 

Relevant articles and documents

Nucleophilic β-alkenylation of N-alkoxyenamines: An umpolung strategy for the preparation of β,γ-unsaturated ketones

An umpolung strategy has been developed for the synthesis of β,γ-unsaturated ketones utilizing nucleophilic β-alkenylation of N-alkoxyenamines, which are prepared in situ from ketones and isoxazolidine, with alkenyl aluminum reagents. Various β,γ-unsatura

Enamine Chemistry. Part 27. The Effect of Additional α- and β-Heteroatoms on the p?-Conjugation and Reactivity of Enamines. Sub- or Super-Enamines?

Enamines derived from isoxazolidine and 1,3-dioxa-5-azacyclohexane have been prepared.The effect of the addition a α- or β-heteroatoms is to decrease the p?-conjugation between the nitrogen lone pair of electrons and the ?-electrons of the double bond, as reflected in the spectral properties of the enamines and their reactivity with electrophiles.The reasons for this are discussed.