3459-29-8

Basic information

• Product Name: 4-aminophenyl-2-acetamido-2-deoxyglucoside
• Synonyms: 4-aminophenyl-2-acetamido-2-deoxyglucoside
• CAS NO: 3459-29-8
• Molecular Formula: C14H20N2O6
• Molecular Weight: 312.3184
• Mol File: 3459-29-8.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 670.7°Cat760mmHg
• Flash Point: 359.4°C
• Appearance: /
• Density: 1.43g/cm³
• Vapor Pressure: 6.63E-19mmHg at 25°C
• Refractive Index: 1.624
• CAS DataBase Reference: 4-aminophenyl-2-acetamido-2-deoxyglucoside(CAS DataBase Reference)
• NIST Chemistry Reference: 4-aminophenyl-2-acetamido-2-deoxyglucoside(3459-29-8)
• EPA Substance Registry System: 4-aminophenyl-2-acetamido-2-deoxyglucoside(3459-29-8)

Safety Data

• Hazardous Substances Data: 3459-29-8(Hazardous Substances Data)

Usage

InChI:InChI=1/C14H20N2O6/c1-7(18)16-11-13(20)12(19)10(6-17)22-14(11)21-9-4-2-8(15)3-5-9/h2-5,10-14,17,19-20H,6,15H2,1H3,(H,16,18)/t10-,11-,12-,13-,14?/m1/s1

Upstream product

• 65907-85-9 p-aminophenyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-1-O-β-D-glucopyranoside 
• 3459-18-5 4-nitrophenyl N-acetyl-β-D-glucosaminide 
• 13089-27-5 p-nitrophenyl 2-acetamido-2-deoxy-3,4,6-tri-O-acetyl-β-D-glucopyranoside 
• 100-02-7 4-nitro-phenol 
• 3068-34-6 Acetic acid (2R,3S,4R,5R,6R)-3-acetoxy-2-acetoxymethyl-5-acetylamino-6-chloro-tetrahydro-pyran-4-yl ester 
• 3006-60-8 2-acetamido-1,3,4,6-tetra-O-acetyl-2-deoxy-β-D-glucopyranose 

Downstream Products

• 135253-87-1 p-Acryloylaminophenyl 2-acetamido-2-deoxy-β-D-glucopyranoside 

Relevant articles and documents

Synthesis and biodistribution studies of carbohydrate derivatives radiolabeled with technetium-99m

Three carbohydrate derivatives, MAG3-Gl, MAG3-Ga, MAG3-NG, were synthesized and radiolabeled in high yields. These substances were injected in health Swiss mice and their biodistribution were evaluated. Among them, 99

Synthesis of 4-aminophenyl N-acetyl-β-D-glucosaminide derivatives and their application to the rate-assay of N-acetyl-β-D-glucosaminidase

Four N-acetyl-β-D-glucosaminides, 4-amino-2,6-dibromophenyl (1a), 4-amino-2,6-dichlorophenyl (1b), 4-amino-2-chlorophenyl (1c) and 4-aminophenyl N-acetyl-β-D-glucosaminides (1d) were synthesized. Substrates lac were hydrolyzed by N-acetyl-β-D-glucosaminid

Syntheses and Transformations of Glycohydrolase Substrates into Protein Conjugates Based on Michael Additions

The glycosyl chloride 1 and bromides 2 and 3 were stereospecifically transformed into p-nitrophenyl glycosides by phase transfer catalysis; these glycohydrolase substrates were reduced and N-acryloylated to afford Michael acceptors which reacted with amine functions of proteins.