152697-19-3

Basic information

• Product Name: phenyl 2-O-acetyl-3,4,6-tri-O-Benzyl-1-seleno-α-D-mannopyranoside
• Synonyms: phenyl 2-O-acetyl-3,4,6-tri-O-Benzyl-1-seleno-α-D-mannopyranoside
• CAS NO: 152697-19-3
• Molecular Weight: 631.627
• Mol File: 152697-19-3.mol

Chemical Properties

• CAS DataBase Reference: phenyl 2-O-acetyl-3,4,6-tri-O-Benzyl-1-seleno-α-D-mannopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: phenyl 2-O-acetyl-3,4,6-tri-O-Benzyl-1-seleno-α-D-mannopyranoside(152697-19-3)
• EPA Substance Registry System: phenyl 2-O-acetyl-3,4,6-tri-O-Benzyl-1-seleno-α-D-mannopyranoside(152697-19-3)

Safety Data

• Hazardous Substances Data: 152697-19-3(Hazardous Substances Data)

Upstream product

• 645-96-5 Benzeneselenol 
• 146864-77-9 3,4,6-tri-O-benzyl-1,2-O-(exo-methoxyethylidene)-β-D-mannopyranose 
• 16697-49-7 3,4,6-tri-O-benzyl-1,2-O-(methoxyethylidene)-β-D-mannopyranose 
• 68681-00-5 3,4,6-tri-O-benzyl-1,2-O-<1-(R)-methoxyethylidene>-β-D-mannopyranose 

Downstream Products

• 221678-96-2 ethyl 2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl-(1->2)-3,4,6-tri-O-benzyl-thio-α-D-mannopyranoside 
• 254444-67-2 Methyl 2,4-di-O-benzyl-3-O-[3,4,6-tri-O-benzyl-2-O-(2',2',2'-trichloroethoxycarbonyl)-α-D-mannopyranosyl]-6-O-tert-butyldiphenylsilyl-α-D-mannopyranoside 
• 254444-13-8 Methyl 2,4-di-O-benzyl-3-O-[3,4,6-tri-O-benzyl-2-O-(2',2',2'-trichloroethoxycarbonyl)-α-D-mannopyranosyl]-α-D-mannopyranoside 
• 254444-10-5 Phenyl 3,4,6-tri-O-benzyl-1-seleno-2-O-(2',2',2'-trichloroethoxycarbonyl)-α-D-mannopyranoside 
• 254444-15-0 Phenyl 3,4,6-tri-O-benzyl-1-seleno-2-O-allyloxycarbonyl-α-D-mannopyranoside 
• 206195-70-2 phenyl 3,4,6-tri-O-Benzyl-1-seleno-α-D-mannopyranoside 

Relevant articles and documents

1,2,5-Ortho esters of D-arabinose as versatile arabinofuranosidic building blocks. Concise synthesis of the tetrasaccharidic cap of the lipoarabinomannan of Mycobacterium tuberculosis

1,2,5-ortho esters of D-arabinose were found to be ideally suited building blocks for the stereoselective formation of and β arabinofuranosidic linkages after nucleophilic opening of the orthoester with oxygen and sulfur nucleophiles; the tetrasaccharidic cap of the lipoarabinomannan of Mycobacterium tuberculosis was then synthesized in a highly convergent manner.

Synthesis of high-mannose type neoglycolipids: Active targeting of liposomes to macrophages in gene therapy

The concise synthesis of five biantennary oligomannose neoglycolipids is presented. Employing a strategy based on the principles of reactivity tuning and orthogonal activation, the oligomannose moieties, isolated from the glycoprotein 63 of the parasite L

Synthesis of glycans from the glycodelins: Two undeca-, two deca-, three nona-, an octa- and a heptasaccharide

The concise synthesis of nine diantennary oligosaccharides by chemical and chemoenzymatic protocols is presented. The compounds display Lewis X, Lewis Y, sialyl Lewis X and T-antigen epitopes supported on a 3,6-branched trimannose core. A chemical approach was adopted for the synthesis of the unsymmetrically decorated structures and those that could not be accessed by enzymatic decoration of a core heptasaccharide.

Chemical synthesis of the W-glycans of gp63, the major surface glycoprotein from Leishmania mexicana amazonemis

The chemical synthesis of the conjugated heptasaccharide Man(α1-3)Man(α1-6)[GIc(α1-3)Man(α1-2)Man(α1-2) Man(α1-3)]Manβl-O[CH2]8CO2Me 1 and four closely related biantennary oligomannose type structures derived from the glyc