210418-04-5

Basic information

• Product Name: p-Nitrophenyl 2-Azido-2-deoxy-a-D-galactopyranoside
• Synonyms: p-Nitrophenyl 2-Azido-2-deoxy-α-D-galactopyranoside;4-Nitrophenyl 2-azido-2-deoxy-α-D-galactopyranoside;4-Nitrophenyl 2-azido-2-deoxy-alpha-D-galactopyranoside;4-nitrophenyl 2-azido-2-deoxyhexopyranoside
• CAS NO: 210418-04-5
• Molecular Formula: C₁₂H₁₄N₄O₇
• Molecular Weight: 0
• EINECS: 1533716-785-6
• Product Categories: 13C & 2H Sugars;Carbohydrates & Derivatives
• Mol File: 210418-04-5.mol

Chemical Properties

• Melting Point: 170-172°C
• Appearance: /
• Storage Temp.: Refrigerator, Under Inert Atmosphere
• Solubility: DMSO (Slightly), Methanol (Slightly)
• CAS DataBase Reference: p-Nitrophenyl 2-Azido-2-deoxy-a-D-galactopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: p-Nitrophenyl 2-Azido-2-deoxy-a-D-galactopyranoside(210418-04-5)
• EPA Substance Registry System: p-Nitrophenyl 2-Azido-2-deoxy-a-D-galactopyranoside(210418-04-5)

Safety Data

• Hazardous Substances Data: 210418-04-5(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
p-Nitrophenyl 2-Azido-2-deoxy-α-D-galactopyranoside is used as a synthetic building block for the creation of complex organic molecules. Its unique structure allows for selective reactions and functional group manipulations, making it a versatile compound in the synthesis of various organic molecules.
Used in Chemical Research:
In the field of chemical research, p-Nitrophenyl 2-Azido-2-deoxy-α-D-galactopyranoside serves as a valuable tool for studying the reactivity and properties of sugar derivatives. Its azido and p-nitrophenyl groups can be used to probe the interactions of these functional groups with other molecules, providing insights into the mechanisms of various chemical reactions.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, p-Nitrophenyl 2-Azido-2-deoxy-α-D-galactopyranoside could potentially be used in the pharmaceutical industry as a starting material for the development of new drugs. Its unique structure and reactivity may allow for the creation of novel compounds with potential therapeutic applications.
Used in Material Science:
In material science, p-Nitrophenyl 2-Azido-2-deoxy-α-D-galactopyranoside could be employed in the development of new materials with specific properties. Its unique structure and reactivity may contribute to the creation of materials with tailored characteristics, such as improved mechanical strength, thermal stability, or chemical resistance.

InChI:InChI=1/C12H14N4O7/c13-15-14-9-11(19)10(18)8(5-17)23-12(9)22-7-3-1-6(2-4-7)16(20)21/h1-4,8-12,17-19H,5H2

Upstream product

• 83025-20-1 3,4,6-tri-O-acetyl-2-azido-2-deoxy-α-D-galactopyranosyltrichloroacetimidate 
• 1147438-51-4 p-nitrophenyl 3,4,6-tri-O-acetyl-2-azido-2-deoxy-α-D-galactopyranoside 
• 100-02-7 4-nitro-phenol 

Downstream Products

• 1316823-00-3 p-nitrophenyl 2-azido-3-O-benzoyl-2-deoxy-4,6-O-p-methoxybenzylidene-α-D-galactopyranoside 
• 1316823-01-4 p-nitrophenyl 2-azido-3-O-benzoyl-2-deoxy-α-D-galactopyranoside 
• 1316823-14-9 p-nitrophenyl 2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl-(1->3)-2-azido-2-deoxy-4,6-O-p-methoxybenzylidene-α-D-galactopyranoside 
• 1316823-18-3 p-nitrophenyl 2-acetamido-4,6-di-O-benzoyl-2,3-N,O-carbonyl-2-deoxy-β-D-glucopyranosyl-(1->3)-2-azido-2-deoxy-4,6-O-p-methoxybenzylidene-α-D-galactopyranoside 
• 1316823-20-7 p-nitrophenyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1->3)-2-azido-2-deoxy-4,6-O-p-methoxybenzylidene-α-D-galactopyranoside 
• 1316823-21-8 p-nitrophenyl 2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl-(1->3)-2-azido-2-deoxy-α-D-galactopyranoside 
• 1316823-22-9 p-nitrophenyl 2-acetamido-4,6-di-O-benzoyl-2,3-N,O-carbonyl-2-deoxy-β-D-glucopyranosyl-(1->3)-2-azido-2-deoxy-α-D-galactopyranoside 
• 1316823-24-1 p-nitrophenyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1->3)-2-azido-2-deoxy-α-D-galactopyranoside 
• 1316823-32-1 p-nitrophenyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1->3)-3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1->6)-2-azido-2-deoxy-α-D-galactopyranoside 
• 1316823-35-4 p-nitrophenyl 2-acetamido-4,6-di-O-benzoyl-2,3-N,O-carbonyl-2-deoxy-β-D-glucopyranosyl-(1->6)-2-azido-3-O-benzoyl-2-deoxy-α-D-galactopyranoside 
• 1316823-36-5 p-nitrophenyl 3,4,6-tri-O-acetyl-2-azido-2-deoxy-α-D-galactopyranosyl-(1->6)-2-azido-3-O-benzoyl-2-deoxy-α-D-galactopyranoside 
• 162792-49-6 p-aminophenyl β-D-galactopyranosyl-(1->3)-2-acetamido-2-deoxy-α-D-galactopyranoside 
• 125455-64-3 p-nitrophenyl 2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->3)-2-acetamido-2-deoxy-α-D-galactopyranoside 
• 1316822-77-1 p-aminophenyl 2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->3)-2-acetamido-2-deoxy-α-D-galactopyranoside 

Relevant articles and documents

Synthesis of mucin O-glycan core structures as their p-nitro- and p-aminophenyl glycosides

For the investigation of glycosidases, and for the construction of glycan arrays the p-nitrophenyl- and p-aminophenyl glycosides of mucin O-glycan core structures 1-7 and the 2,6-ST-antigen have been chemically synthesized using d-galactose as a precursor for GalNAc residues. GlcNAc residues have partly been introduced using a 4,6-di-O-benzoyl-2,3-N,O-oxazolidinone-protected donor, which allowed deprotection of the formed di- and tri-saccharides in one step using sodium methoxide.