189218-66-4

Basic information

• Product Name: pent-4-enyl (3,4,6-tri-O-acetyl-2-deoxy-2-tetrachlorophthalimido-β-D-glucopyranosyl)-(1->6)-3-O-benzoyl-4-O-benzyl-2-deoxy-2-(pent-4-enoylamino)-β-D-glucopyranoside
• Synonyms: pent-4-enyl (3,4,6-tri-O-acetyl-2-deoxy-2-tetrachlorophthalimido-β-D-glucopyranosyl)-(1->6)-3-O-benzoyl-4-O-benzyl-2-deoxy-2-(pent-4-enoylamino)-β-D-glucopyranoside
• CAS NO: 189218-66-4
• Molecular Weight: 1078.78
• Mol File: 189218-66-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: pent-4-enyl (3,4,6-tri-O-acetyl-2-deoxy-2-tetrachlorophthalimido-β-D-glucopyranosyl)-(1->6)-3-O-benzoyl-4-O-benzyl-2-deoxy-2-(pent-4-enoylamino)-β-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: pent-4-enyl (3,4,6-tri-O-acetyl-2-deoxy-2-tetrachlorophthalimido-β-D-glucopyranosyl)-(1->6)-3-O-benzoyl-4-O-benzyl-2-deoxy-2-(pent-4-enoylamino)-β-D-glucopyranoside(189218-66-4)
• EPA Substance Registry System: pent-4-enyl (3,4,6-tri-O-acetyl-2-deoxy-2-tetrachlorophthalimido-β-D-glucopyranosyl)-(1->6)-3-O-benzoyl-4-O-benzyl-2-deoxy-2-(pent-4-enoylamino)-β-D-glucopyranoside(189218-66-4)

Safety Data

• Hazardous Substances Data: 189218-66-4(Hazardous Substances Data)

Upstream product

• 189218-60-8 pent-4-enyl 3,6-di-O-benzoyl-4-O-benzyl-2-deoxy-2-(pent-4-enoylamino)-β-D-glucopyranoside 
• 189218-59-5 pent-4-enyl 3,6-di-O-benzoyl-2-deoxy-2-(pent-4-enoylamino)-β-D-glucopyranoside 
• 174356-26-4 1,3,4,6-tetra-O-acetyl-2-deoxy-2-(3,4,5,6-tetra-chlorophthalimido)-D-glucospyranose 
• 163926-96-3 Pent-4-enyl 3,4,6-tri-O-acetyl-2-deoxy-2-(pent-4-enoylamino)-β-D-glucopyranoside 
• 100-39-0 benzyl bromide 
• 189218-64-2 3,4,6-tri-O-acetyl-2-deoxy-2-tetrachlorophthalimido-α,β-D-glucopyranosyl bromide 
• 189218-61-9 pent-4-enyl 3-O-benzoyl-4-O-benzyl-2-deoxy-2-(pent-4-enoylamino)-β-D-glucopyranoside 

Relevant articles and documents

Studies toward lipid A: Synthesis of differentially protected disaccharide fragments

Disaccharides containing two glucosamine units are readily synthesized where the two amine functionalities are orthogonally protected as the tetrachlorophthaloyl and pent-4-enoyl moieties. The 1→6 linked disaccharide has the potential to be developed toward a series of biologically interesting lipid A analogs.