158006-53-2

Basic information

• Product Name: 3,3'-Di-O-hexadecamethylenedi-sn-glycerol 1,1'-bis(3'-nitrobenzenesulfonate)
• Synonyms: 3,3'-Di-O-hexadecamethylenedi-sn-glycerol 1,1'-bis(3'-nitrobenzenesulfonate)
• CAS NO: 158006-53-2
• Molecular Weight: 776.924
• Mol File: 158006-53-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3,3'-Di-O-hexadecamethylenedi-sn-glycerol 1,1'-bis(3'-nitrobenzenesulfonate)(CAS DataBase Reference)
• NIST Chemistry Reference: 3,3'-Di-O-hexadecamethylenedi-sn-glycerol 1,1'-bis(3'-nitrobenzenesulfonate)(158006-53-2)
• EPA Substance Registry System: 3,3'-Di-O-hexadecamethylenedi-sn-glycerol 1,1'-bis(3'-nitrobenzenesulfonate)(158006-53-2)

Safety Data

• Hazardous Substances Data: 158006-53-2(Hazardous Substances Data)

Upstream product

• 7735-42-4 1,16-hexadecanediol 
• 115314-14-2 (R)-glycidyl nosylate 

Downstream Products

• 157999-17-2 2,2'-Di-O-octyl-3,3'-di-O-hexadecamethylenedi-sn-glycerol 1,1'-bis(3'-nitrobenzenesulfonate) 

Relevant articles and documents

Synthesis of Chiral Diether and Tetraether Phospholipids: Regiospecific Ring Opening of Epoxy Alcohol Intermediates Derived from Asymmetric Epoxidation

Diether and tetraether phospholipids have been synthesized using chiral epoxy alcohol starting materials (e.g. glycidol 3-nitrobenzenesulfonate esters or tert-butyldiphenylsilyl ethers).These chiral precursors provide control over the stereochemistry, sub