1192256-26-0

Basic information

• Product Name: benzyl 4-O-(hex-5-enoyl)-6-O-propargyl-2,3-dideoxy-α-D-erythro-hex-2-enpyranoside
• Synonyms: benzyl 4-O-(hex-5-enoyl)-6-O-propargyl-2,3-dideoxy-α-D-erythro-hex-2-enpyranoside
• CAS NO: 1192256-26-0
• Molecular Weight: 370.445
• Mol File: 1192256-26-0.mol

Chemical Properties

• CAS DataBase Reference: benzyl 4-O-(hex-5-enoyl)-6-O-propargyl-2,3-dideoxy-α-D-erythro-hex-2-enpyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl 4-O-(hex-5-enoyl)-6-O-propargyl-2,3-dideoxy-α-D-erythro-hex-2-enpyranoside(1192256-26-0)
• EPA Substance Registry System: benzyl 4-O-(hex-5-enoyl)-6-O-propargyl-2,3-dideoxy-α-D-erythro-hex-2-enpyranoside(1192256-26-0)

Safety Data

• Hazardous Substances Data: 1192256-26-0(Hazardous Substances Data)

Upstream product

• 1577-22-6 5-hexenoic acid 
• 1192256-23-7 benzyl 6-O-propargyl-2,3-dideoxy-α-D-erythro-hex-2-enpyranoside 

Relevant articles and documents

Synthesis of macrocyclic scaffolds suitable for diversity-oriented synthesis of macrolides

Synthesis of macrocyclic glycal-based scaffolds for diversity-oriented synthesis was studied and demonstrated using macrocyclic enyne ring-closing metathesis. The roles of ring size, alkyne substitution, and orientation relative to the glycal were studied. In all cases, the cyclization showed preference for the thermodynamically favored endo-mode of closure and a trans-double bond at the ring-closure site, leaving macrocyclic scaffolds all containing multiple orthogonal functional groups available for further diversification.