243469-59-2

Basic information

• Product Name: 2,5-Anhydro-1-azido-1-deoxy-D-glucitol
• Synonyms: 2,5-Anhydro-1-azido-1-deoxy-D-Glucitol
• CAS NO: 243469-59-2
• Molecular Formula: C₆H₁₁N₃O₄
• Molecular Weight: 189.17
• Product Categories: Sugars
• Mol File: 243469-59-2.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,5-Anhydro-1-azido-1-deoxy-D-glucitol(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-Anhydro-1-azido-1-deoxy-D-glucitol(243469-59-2)
• EPA Substance Registry System: 2,5-Anhydro-1-azido-1-deoxy-D-glucitol(243469-59-2)

Safety Data

• Hazardous Substances Data: 243469-59-2(Hazardous Substances Data)

Usage

General Description

2,5-Anhydro-1-azido-1-deoxy-D-glucitol, also known as 1-azido-1-deoxy-D-sorbitol, is a chemical compound that belongs to the family of azido sugars. It is a synthetic intermediate used in the preparation of nucleotide sugar analogs and has potential applications in drug discovery and glycobiology research. 2,5-Anhydro-1-azido-1-deoxy-D-glucitol has been studied for its antiviral and antifungal properties, as well as its potential use as a prodrug delivery system. Its structure and properties make it a promising candidate for further development in the field of carbohydrate chemistry and bioorganic chemistry.

InChI:InChI=1/C6H11N3O4/c7-9-8-1-3-5(11)6(12)4(2-10)13-3/h3-6,10-12H,1-2H2/t3-,4+,5+,6+/m0/s1

Upstream product

• 157363-84-3 1,2:5,6-dianhydro-3,4-di-O-benzyl-L-iditol 
• 102093-93-6 2,5-anhydro-3,4-di-O-benzyl-1-bromo-1-deoxy-D-glucitol 
• 36199-02-7 3,4-di-O-benzyl-D-mannitol 
• 1309924-06-8 2,5-anhydro-1-bromo-1-deoxy-D-glucitol 
• 27826-73-9 2,5-anhydro-D-glucitol 
• 82064-07-1 2,5-anhydro-4,5-di-O-benzoyl-1-O-p-tolylsulfonyl-D-glucitol 
• 75499-82-0 2,5-anhydro-4,5-di-O-benzoyl-1,3-O-isopropylidene-D-glucitol 
• 75499-83-1 2,5-anhydro-4,5-di-O-benzoyl-D-glucitol 
• 65729-81-9 2,5-anhydro-1,3-O-isopropylidene-D-glucitol 
• 243132-01-6 2,5-anhydro-1-azido-4,5-di-O-benzoyl-1-deoxy-D-glucitol 

Downstream Products

• 1309855-93-3 1-(3,4,6-tri-O-acetyl-2,5-anhydro-1-deoxy-D-glucitolyl)-4-(4-N,N-dimethylaminophenyl)-[1,2,3]-triazole 
• 1309855-95-5 1-(3,4,6-tri-O-acetyl-2,5-anhydro-1-deoxy-D-glucitolyl)-4-(4-methoxyphenyl)-[1,2,3]-triazole 
• 1309855-98-8 1-(3,4,6-tri-O-acetyl-2,5-anhydro-1-deoxy-D-glucitolyl)-4-(1-hydroxy-1-phenylmethyl)-[1,2,3]-triazole 
• 1309855-99-9 1-(3,4,6-tri-O-acetyl-2,5-anhydro-1-deoxy-D-glucitolyl)-4-(1-hydroxycyclohexyl)-[1,2,3]-triazole 
• 1309856-04-9 1-(3,4,6-tri-O-acetyl-2,5-anhydro-1-deoxy-D-glucitolyl)-4-(4-aminophenyl)-[1,2,3]-triazole 
• 1309856-08-3 1-(3,4,6-tri-O-acetyl-2,5-anhydro-1-deoxy-D-glucitolyl)-4-(4-hydroxymethylphenyl)-[1,2,3]-triazole 
• 1309856-11-8 1-(2,5-anhydro-1-deoxy-D-glucitolyl)-4-(4-N,N-dimethylaminophenyl)-[1,2,3]-triazole 
• 1309856-13-0 1-(2,5-anhydro-1-deoxy-D-glucitolyl)-4-(4-methoxyphenyl)-[1,2,3]-triazole 
• 1309856-17-4 1-(2,5-anhydro-1-deoxy-D-glucitolyl)-4-(1-hydroxy-1-phenylmethyl)-[1,2,3]-triazole 
• 1309856-18-5 1-(2,5-anhydro-1-deoxy-D-glucitolyl)-4-(1-hydroxycyclohexyl)-[1,2,3]-triazole 
• 1309856-23-2 1-(2,5-anhydro-1-deoxy-D-glucitolyl)-4-(4-aminophenyl)-[1,2,3]-triazole 
• 1309856-24-3 1-(2,5-anhydro-1-deoxy-6-sulfo-D-glucitolyl)-4-(4-N,N-dimethylaminophenyl)-[1,2,3]-triazole 
• 1309856-26-5 1-(2,5-anhydro-1-deoxy-6-sulfo-D-glucitolyl)-4-(4-methoxyphenyl)-[1,2,3]-triazole 
• 1309856-30-1 1-(2,5-anhydro-1-deoxy-6-sulfo-D-glucitolyl)-4-(1-hydroxycyclohexyl)-[1,2,3]-triazole 

Relevant articles and documents

An efficient approach to 2,5-anhydro-glucitol-based 1′-homo-N- nucleoside mimetics

This Letter describes an efficient synthesis of a range of 1′-homo-N-nucleoside mimetics with a series of 4-substituted 1,2,3-triazoles replacing the natural nucleobase. The synthesis of 6-O-monosulfated 1′-homo-N-nucleoside mimetic derivatives is also discussed.