104023-30-5

Basic information

• Product Name: Cyclohexene, 4-(azidomethyl)-
• CAS NO: 104023-30-5
• Molecular Formula: C7H11N3
• Molecular Weight: 137.184
• Mol File: 104023-30-5.mol

Chemical Properties

• CAS DataBase Reference: Cyclohexene, 4-(azidomethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexene, 4-(azidomethyl)-(104023-30-5)
• EPA Substance Registry System: Cyclohexene, 4-(azidomethyl)-(104023-30-5)

Safety Data

• Hazardous Substances Data: 104023-30-5(Hazardous Substances Data)

Upstream product

• 92864-78-3 cyclohex-3-en-1-ylmethyl 4-methylbenzenesulfonate 
• 72581-32-9 cyclohex-3-enylmethanol 
• 108541-48-6 [(cyclohex-3-en-1-yl)methyl]methanesulfonate 

Downstream Products

• 1224697-33-9 1-[(cyclohex-3-en-1-yl)methyl]-4-(trifluoroacetamidomethyl)-1,2,3-triazole 
• 142991-91-1 acetoxyacetic acid 
• 158213-00-4 (hydroxy)acetic acid 
• 32591-23-4 methyl N-<(3-cyclohexen-1-yl)methyl>carbamate 
• 128892-12-6 (phenylthio)acetic acid methyl ester 
• 128911-32-0 N-(2-(1-cyclohexen-1-yl)ethyl)-N-(methoxycarbonyl)glycine methyl ester 
• 32591-32-5 (3-cyclohexen-1-yl)methylamine hydrochloride 
• 2555-10-4 (3-cyclohexen-1-yl)methylamine 

Relevant articles and documents

Reductive Cyclization of Carbon-Centered Glycine Radicals; A Novel Synthetic Route to Cyclic α-Amino Acids

Reductive cyclizations (tributyltin hydride, AIBN) of several α-(phenylthio)glycine derivatives with a 3-alkenyl substituent at nitrogen are reported.These reactions proceed via 2-aza-5-alken-1-yl radicals as intermediates which bear electron-withdrawing

Reduction d'azides par la triphenylphosphine en presence d'eau : une methode generale et chimioselective d'acces aux amines primaires

The reaction of azides with one equivalent of triphenylphosphine in the presence of a slight excess of water in THF leads quantitatively to the corresponding primary amines.This transformation is chemoselective.