1197190-18-3

Basic information

• Product Name: (E)-3-((S)-2-((R)-3-(4-methoxybenzyloxy)-1-(methoxymethoxy)propyl)oxiran-2-yl)prop-2-en-1-ol
• Synonyms: (E)-3-((S)-2-((R)-3-(4-methoxybenzyloxy)-1-(methoxymethoxy)propyl)oxiran-2-yl)prop-2-en-1-ol
• CAS NO: 1197190-18-3
• Molecular Weight: 338.401
• Mol File: 1197190-18-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (E)-3-((S)-2-((R)-3-(4-methoxybenzyloxy)-1-(methoxymethoxy)propyl)oxiran-2-yl)prop-2-en-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-3-((S)-2-((R)-3-(4-methoxybenzyloxy)-1-(methoxymethoxy)propyl)oxiran-2-yl)prop-2-en-1-ol(1197190-18-3)
• EPA Substance Registry System: (E)-3-((S)-2-((R)-3-(4-methoxybenzyloxy)-1-(methoxymethoxy)propyl)oxiran-2-yl)prop-2-en-1-ol(1197190-18-3)

Safety Data

• Hazardous Substances Data: 1197190-18-3(Hazardous Substances Data)

Upstream product

• 1197190-08-1 (E)-ethyl 3-((S)-2-((R)-3-(4-methoxybenzyloxy)-1-(methoxymethoxy)propyl)oxiran-2-yl)acrylate 
• 147-79-5 rochelle salt 

Downstream Products

• 1197190-19-4 (E)-3-((S)-2-((R)-3-(4-methoxybenzyloxy)-1-(methoxymethoxy)propyl)oxiran-2-yl)acrylaldehyde 

Relevant articles and documents

Enantio- and stereoselective route to the phoslactomycin family of antibiotics: Formal synthesis of (+)-fostriecin and (+)-phoslactomycin B

A general methodology applicable for the synthesis of the phoslactomycin family of antibiotics, potent and selective protein phosphatase inhibitors, has been developed starting from a β-isocupreidine-catalyzed asymmetric Baylis-Hillman reaction of 3-(4-me