1221966-90-0

Basic information

• Product Name: N-((4S,5R,E)-8-chloro-5-(methoxymethoxy)-2-methyloct-6-en-4-yl)benzamide
• Synonyms: N-((4S,5R,E)-8-chloro-5-(methoxymethoxy)-2-methyloct-6-en-4-yl)benzamide
• CAS NO: 1221966-90-0
• Molecular Weight: 339.862
• Mol File: 1221966-90-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-((4S,5R,E)-8-chloro-5-(methoxymethoxy)-2-methyloct-6-en-4-yl)benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-((4S,5R,E)-8-chloro-5-(methoxymethoxy)-2-methyloct-6-en-4-yl)benzamide(1221966-90-0)
• EPA Substance Registry System: N-((4S,5R,E)-8-chloro-5-(methoxymethoxy)-2-methyloct-6-en-4-yl)benzamide(1221966-90-0)

Safety Data

• Hazardous Substances Data: 1221966-90-0(Hazardous Substances Data)

Upstream product

• 1221966-84-2 N-((4S,5R,E)-8-chloro-5-hydroxy-2-methyloct-6-en-4-yl)benzamide 
• 150587-19-2 methoxymethoxy chloride 

Downstream Products

• 1221967-02-7 (4S,5S,6S)-4-isobutyl-5-(methoxymethoxy)-2-phenyl-6-vinyl-5,6-dihydro-4H-1,3-oxazine 
• 1221967-03-8 (4S,5S,6R)-4-isobutyl-5-(methoxymethoxy)-2-phenyl-6-vinyl-5,6-dihydro-4H-1,3-oxazine 

Relevant articles and documents

Stereoselective intramolecular cyclization of γ-allylbenzamide via π-allylpalladium complex catalyzed by Pd(0)

An efficient procedure for synthesizing oxazines was developed by the palladium(0)-catalyzed intramolecular cyclization of a benzamide through a π-allylpalladium (II) complex. Interestingly, the diastereoselectivity of oxazine ring formation was dominantly controlled by the bulkiness of various protecting groups on the secondary alcohols.