1192256-28-2

Basic information

• Product Name: benzyl 4-O-(non-8-enoyl)-6-O-propargyl-2,3-dideoxy-α-D-erythro-hex-2-enpyranoside
• Synonyms: benzyl 4-O-(non-8-enoyl)-6-O-propargyl-2,3-dideoxy-α-D-erythro-hex-2-enpyranoside
• CAS NO: 1192256-28-2
• Molecular Weight: 412.526
• Mol File: 1192256-28-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: benzyl 4-O-(non-8-enoyl)-6-O-propargyl-2,3-dideoxy-α-D-erythro-hex-2-enpyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl 4-O-(non-8-enoyl)-6-O-propargyl-2,3-dideoxy-α-D-erythro-hex-2-enpyranoside(1192256-28-2)
• EPA Substance Registry System: benzyl 4-O-(non-8-enoyl)-6-O-propargyl-2,3-dideoxy-α-D-erythro-hex-2-enpyranoside(1192256-28-2)

Safety Data

• Hazardous Substances Data: 1192256-28-2(Hazardous Substances Data)

Upstream product

• 31642-67-8 non-8-enoic 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.