1-Azido-1-deoxy-β-D-glucopyranoside tetraacetate

• Catalog No.: 513997
• CAS Number: 13992-25-1
• M. F.: C14H19N3O9
• M. W.: 373.31536

SYNONYMS

• Title: 1-叠氮-1-脱氧-β-D-吡喃葡萄糖苷四乙酸酯
• IUPAC name: [(2R,3S,4S,5R,6R)-3,4,5-tris(acetyloxy)-6-azidooxan-2-yl]methyl acetate
• IUPAC Traditional name: [(2R,3S,4S,5R,6R)-3,4,5-tris(acetyloxy)-6-azidooxan-2-yl]methyl acetate
• Synonyms: NSC 272456

DATABASE IDS

• MDL Number: MFCD00181721
• CAS Number: 13992-25-1
• PubChem SID: 24873728

PROPERTIES

• Empirical Formula (Hill Notation): C14H19N3O9
• Melting Point: 127-131 °C(lit.)
• Optical Rotation: [α]/D -29°, c = 1% in H2O
• Optical Rotation: [α]/D -30°, c = 1% in chloroform
• Personal Protective Equipment: Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
• German water hazard class: 3

DETAILS

Description (简体中文)

包装
1 g in glass bottle
Application
Reactant for:
• Synthesis of Protein Tyrosine Phosphatase 1B inhibitor1
• Synthesis of glycoconjugate carbonic anhydrase inhibitors by ruthenium-catalyzed azide-alkyne 1,3-dipolar cycloaddition2
• Synthesis of variously coupled conjugates of D-glucose via click chemistry for inhibition of glycogen phosphorylase3
• Hydrogenation reactions4
• Preparation of posttranslationally modified peptides efficiently mimicking neoantigens in relation to autoimmune disease5

Description (English)

Packaging
1 g in glass bottle
Application
Reactant for:
• Synthesis of Protein Tyrosine Phosphatase 1B inhibitor1
• Synthesis of glycoconjugate carbonic anhydrase inhibitors by ruthenium-catalyzed azide-alkyne 1,3-dipolar cycloaddition2
• Synthesis of variously coupled conjugates of D-glucose via click chemistry for inhibition of glycogen phosphorylase3
• Hydrogenation reactions4
• Preparation of posttranslationally modified peptides efficiently mimicking neoantigens in relation to autoimmune disease5