131605-19-1

Basic information

• Product Name: 4H-Cyclopent[d]isoxazole,3a,5,6,6a-tetrahydro-3-(1-propenyl)-(9CI)
• Synonyms: 4H-Cyclopent[d]isoxazole,3a,5,6,6a-tetrahydro-3-(1-propenyl)-(9CI)
• CAS NO: 131605-19-1
• Molecular Formula: C9H13NO
• Molecular Weight: 151.20562
• Product Categories: CYCLOPENTANE
• Mol File: 131605-19-1.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4H-Cyclopent[d]isoxazole,3a,5,6,6a-tetrahydro-3-(1-propenyl)-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 4H-Cyclopent[d]isoxazole,3a,5,6,6a-tetrahydro-3-(1-propenyl)-(9CI)(131605-19-1)
• EPA Substance Registry System: 4H-Cyclopent[d]isoxazole,3a,5,6,6a-tetrahydro-3-(1-propenyl)-(9CI)(131605-19-1)

Safety Data

• Hazardous Substances Data: 131605-19-1(Hazardous Substances Data)

Upstream product

• 5314-34-1 crotonaldoxime 
• 142-29-0 cyclopentene 

Relevant articles and documents

Reactions with α,β-Unsaturated Nitrile Oxides. Synthetic Studies in the Terpene Field. Synthesis of Tagetones, Ocimenones, Deodarone and Atlantone

The generation and 1,3-dipolar cycloaddition of α,β-unsaturated nitrile oxides are described.Selective reductive cleavage of the isoxazoline ring was achived.Subsequent elimination of water leads to the 1,4-dien-3-one system.The formation of tetrahydro-γ-pyrones is observed.The reactions were applied to the synthesis of tagetones, ocimenones, deodarone and atlantone.