511274-73-0

Basic information

• Product Name: Pent-4-enoic acid (2R,3R,4R,5S,6S)-4,5-dimethoxy-2-pent-4-enoyloxymethyl-6-phenyl-tetrahydro-pyran-3-yl ester
• Synonyms: Pent-4-enoic acid (2R,3R,4R,5S,6S)-4,5-dimethoxy-2-pent-4-enoyloxymethyl-6-phenyl-tetrahydro-pyran-3-yl ester
• CAS NO: 511274-73-0
• Molecular Weight: 432.514
• Mol File: 511274-73-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Pent-4-enoic acid (2R,3R,4R,5S,6S)-4,5-dimethoxy-2-pent-4-enoyloxymethyl-6-phenyl-tetrahydro-pyran-3-yl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Pent-4-enoic acid (2R,3R,4R,5S,6S)-4,5-dimethoxy-2-pent-4-enoyloxymethyl-6-phenyl-tetrahydro-pyran-3-yl ester(511274-73-0)
• EPA Substance Registry System: Pent-4-enoic acid (2R,3R,4R,5S,6S)-4,5-dimethoxy-2-pent-4-enoyloxymethyl-6-phenyl-tetrahydro-pyran-3-yl ester(511274-73-0)

Safety Data

• Hazardous Substances Data: 511274-73-0(Hazardous Substances Data)

Upstream product

• 13231-13-5 (2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)benzene 
• 604-69-3 β-D-glucose pentaacetate 
• 572-09-8 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide 
• 5627-22-5 (2R,3S,4R,5R,6S)-2-(hydroxymethyl)-6-phenyltetrahydro-2H-pyran-3,4,5-triol 
• 511274-47-8 (2R,4aR,6S,7R,8R,8aS)-2,6-Diphenyl-hexahydro-pyrano[3,2-d][1,3]dioxine-7,8-diol 
• 511274-41-2 (2R,4aR,6S,7S,8R,8aR)-7,8-Dimethoxy-2,6-diphenyl-hexahydro-pyrano[3,2-d][1,3]dioxine 
• 511274-72-9 (2R,3R,4S,5S,6S)-2-Hydroxymethyl-4,5-dimethoxy-6-phenyl-tetrahydro-pyran-3-ol 
• 39716-58-0 pent-4-enoyl chloride 

Downstream Products

• 511274-33-2 (E)-(2S,3S,4R,4aR,15aR)-3,4-Dimethoxy-2-phenyl-2,3,4,4a,7,8,11,12,15,15a-decahydro-1,5,14-trioxa-benzocyclotridecene-6,13-dione 

Relevant articles and documents

A convergent ring-closing metathesis approach to carbohydrate-based macrolides with potential antibiotic activity

An efficient convergent approach has been developed for the construction of novel, non-natural, carbohydrate-based macrolides. The key step in the synthesis is the formation of the macrocyclic ring via a ring-closing metathesis reaction. The obtained macrolide analogues have been screened for biological activity against Gram-positive and Gram-negative bacteria, including resistant strains, yeasts, and molds.