103655-68-1

Basic information

• Product Name: 3-hydroxy-2-methylene-N-phenyl-4-<(trimethylsilyl)oxy>dodecanamide
• Synonyms: 3-hydroxy-2-methylene-N-phenyl-4-<(trimethylsilyl)oxy>dodecanamide
• CAS NO: 103655-68-1
• Molecular Weight: 391.626
• Mol File: 103655-68-1.mol

Chemical Properties

• CAS DataBase Reference: 3-hydroxy-2-methylene-N-phenyl-4-<(trimethylsilyl)oxy>dodecanamide(CAS DataBase Reference)
• NIST Chemistry Reference: 3-hydroxy-2-methylene-N-phenyl-4-<(trimethylsilyl)oxy>dodecanamide(103655-68-1)
• EPA Substance Registry System: 3-hydroxy-2-methylene-N-phenyl-4-<(trimethylsilyl)oxy>dodecanamide(103655-68-1)

Safety Data

• Hazardous Substances Data: 103655-68-1(Hazardous Substances Data)

Upstream product

• 103633-65-4 N-phenyl-2-<(phenylseleno)methyl>-4-<(trimethylsilyl)oxy>-2-dodecenamide 
• 124-19-6 nonan-1-al 
• 87504-85-6 N-phenyl-2-<(phenylsulfonyl)methyl>propenamide 
• 103633-59-6 4-hydroxy-2-methylene-N-phenyl-3-(phenylsulfonyl)dodecanamide 
• 103633-62-1 2-methylene-N-phenyl-3-(phenylsulfonyl)-4-<(trimethylsilyl)oxy>dodecanamide 

Downstream Products

• 103633-72-3 trans-3,4-epoxy-2-methylene-N-phenyldodecanamide 
• 103633-72-3 cis-3,4-epoxy-2-methylene-N-phenyldodecanamide 
• 103633-70-1 Methanesulfonic acid (1R,2S)-1-(1-phenylcarbamoyl-vinyl)-2-trimethylsilanyloxy-decyl ester 
• 103633-70-1 Methanesulfonic acid (1R,2R)-1-(1-phenylcarbamoyl-vinyl)-2-trimethylsilanyloxy-decyl ester 

Relevant articles and documents

Dianion of N-Phenyl-2-propenamide as a Versatile Reagent for the Preparation of α-Methylene Carbonyl Compounds

A general synthetic route to α-methylene β-lactams is described that involves the regioselective electrophilic substitution of the dianion 2 generated from N-phenyl-2-propenamide (1).A convergent synthesis of conocandin N-phenylami

A GENERAL METHOD FOR THE SYNTHESIS OF 3,4-EPOXY-2-METHYLENEALKANOIC ACID DERIVATIVES USING DIANION OF N-PHENYL-2-(PHENYLSULFONYLMETHYL)-PROPENAMIDE

A general procedure has been developed for the synthesis of 3,4-epoxy-2-methylenealkanoic acid derivatives using dianion of N-phenyl-2-(phenylsulfonylmethyl)propenamide and aldehydes.