344948-04-5

Basic information

• Product Name: C₁₈H₂₁N₃O₄
• Synonyms: C₁₈H₂₁N₃O₄
• CAS NO: 344948-04-5
• Molecular Weight: 343.382
• Mol File: 344948-04-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₁₈H₂₁N₃O₄(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₈H₂₁N₃O₄(344948-04-5)
• EPA Substance Registry System: C₁₈H₂₁N₃O₄(344948-04-5)

Safety Data

• Hazardous Substances Data: 344948-04-5(Hazardous Substances Data)

Upstream product

• 344948-00-1 Toluene-4-sulfonic acid (R)-2-((3aR,5S,6S,6aR)-2,2-dimethyl-6-[1,2,3]triazol-1-yl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-2-hydroxy-ethyl ester 
• 344947-95-1 1-[(3aR,5S,6S,6aR)-5-((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl]-4-trimethylsilanyl-1H-[1,2,3]triazole 
• 344947-98-4 (R)-1-[(3aR,5S,6S,6aR)-2,2-Dimethyl-6-(4-trimethylsilanyl-[1,2,3]triazol-1-yl)-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl]-ethane-1,2-diol 
• 344947-75-7 1-(5'-O-acetyl-6'-deoxy-6'-iodo-1',2'-O-isopropylidene-α-D-glucofuranosyl)-1,2,3-triazole 
• 344947-78-0 Acetic acid (S)-2-bromo-1-((3aR,5S,6S,6aR)-2,2-dimethyl-6-[1,2,3]triazol-1-yl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-ethyl ester 
• 344947-97-3 1-[(3aR,5S,6S,6aR)-5-((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl]-1H-[1,2,3]triazole 
• 344948-01-2 5-O-acetyl-3-azido-6-bromo-3,6-dideoxy-1,2-O-isopropylidene-α-D-glucofuranose 
• 344947-99-5 (R)-1-((3aR,5S,6S,6aR)-2,2-Dimethyl-6-[1,2,3]triazol-1-yl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-ethane-1,2-diol 
• 262381-06-6 4-trimethylsilyl-1-(6'-bromo-6'-deoxy-1',2'-O-isopropylidene-α-D-glucofuranosyl)-1,2,3-triazole 
• 262381-09-9 C₁₄H₂₃N₃O₄Si 
• 262381-08-8 1-(6'-deoxy-6'-iodo-1',2'-O-isopropylidene-α-D-glucofuranosyl)-1,2,3-triazole 
• 22169-71-7 (R)-1-((3aR,5S,6S,6aR)-6-azido-2,2-dimethyltetrahydrofuro-[2,3-d][1,3]dioxol-5-yl)ethane-1,2-diol 
• 13964-23-3 3-azido-3-deoxy-1,2:5,6-di-(O-isopropylidene)-α-D-glucofuranose 
• 100-39-0 benzyl bromide 

Relevant articles and documents

Free-radical cyclizations onto differently substituted 1,2,3-triazoles installed in sugar templates

The synthesis and manipulation of differently substituted 1,2,3-triazoles (7-11 and 12-16) installed in sugar templates gave compounds 29-34 and 44-50, after reaction with tributyltin hydride or tris(trimethylsilyl)silane. Following standard procedures compound 44 was transformed into piperidinose derivative 54. These compounds are chiral, useful building blocks for the synthesis of glycosidase inhibitors of the fused-azole piperidinose type.