84573-22-8

Basic information

• Product Name: (E)-3-((2S,3R)-3-Benzyloxymethyl-oxiranyl)-acrylic acid methyl ester
• CAS NO: 84573-22-8
• Molecular Weight: 248.279
• Mol File: 84573-22-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (E)-3-((2S,3R)-3-Benzyloxymethyl-oxiranyl)-acrylic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-3-((2S,3R)-3-Benzyloxymethyl-oxiranyl)-acrylic acid methyl ester(84573-22-8)
• EPA Substance Registry System: (E)-3-((2S,3R)-3-Benzyloxymethyl-oxiranyl)-acrylic acid methyl ester(84573-22-8)

Safety Data

• Hazardous Substances Data: 84573-22-8(Hazardous Substances Data)

Upstream product

• 78469-86-0 4-nitro-benzoic acid (2R,3S)-3-benzyloxymethyl-oxiranylmethyl ester 
• 78513-07-2 (-)-(2S,3R)-2,3-epoxy-4-(benzyloxy)-1-butanol 
• 133321-78-5 (2R,3R)-3-[(benzyloxy)methyl]oxirane-2-carbaldehyde 
• 21204-67-1 methyl (triphenylphosphoranylidene)acetate 

Downstream Products

• 138876-64-9 3-((2S,3S)-3-Formyl-oxiranyl)-propionic acid methyl ester 

Relevant articles and documents

ENANTIOSELECTIVE SYNTHESIS OF FOUR ISOMERIC BUILDING BLOCKS USEFUL IN THE SYNTHESIS OF 2-NOR-LEUKOTRIENE ANALOGUES

We report, in this letter, the enantioselective synthesis of four isomeric functionalized epoxides (3a, 3b, 3c and 3d) which are useful building blocks for the synthesis of 2-nor-leukotriene analogues.All four epoxides are formally derived from a single n