76155-50-5

Basic information

• Product Name: ETHYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE
• Synonyms: ETHYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE;Ethyl2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-b-D-glucopyranoside;ETHYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-SS-D-GLUCOPYRANOSIDE;Ethyl-2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranoside;Ethyl 2-(acetylamino)-2-deoxy-beta-D-glucopyranoside-3,4,6-triacetate;Ethyl 2-acetamido-2-deoxy-beta-D-glucopyranoside triacetate;(2R,3S,4R,5R,6R)-5-AcetaMido-2-(acetoxyMethyl)-6-ethoxytetrahydro-2H-pyran-3,4-diyl diacetate;b-D-Glucopyranoside, ethyl2-(acetylamino)-2-deoxy-, 3,4,6-triacetate
• CAS NO: 76155-50-5
• Molecular Formula: C16H25NO9
• Molecular Weight: 375.371
• EINECS: 1533716-785-6
• Mol File: 76155-50-5.mol
• Article Data: 4

Chemical Properties

• Melting Point: 191℃
• Boiling Point: 525℃
• Flash Point: 265℃
• Appearance: /
• Density: 1.24
• Storage Temp.: 2-8°C
• CAS DataBase Reference: ETHYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE(CAS DataBase Reference)
• NIST Chemistry Reference: ETHYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE(76155-50-5)
• EPA Substance Registry System: ETHYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE(76155-50-5)

Safety Data

• Hazardous Substances Data: 76155-50-5(Hazardous Substances Data)

Usage

General Description

ETHYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE is a chemical compound that belongs to the class of carbohydrates, specifically glycosides. It is a derivative of 2-deoxy-beta-D-glucopyranoside, which is a type of sugar molecule. The compound is composed of an ethyl group attached to a sugar molecule, along with acetyl and acetamido groups. This chemical is often used in organic synthesis and as a building block for the creation of more complex molecules. Additionally, it has potential applications in pharmaceutical research and the development of new drugs due to its carbohydrate-based structure.

Upstream product

• 4710-88-7 3,4,6-tri-O-acetyl-2-amino-2-deoxy-α-D-glucopyranosyl bromide hydrobromide 
• 3006-60-8 2-acetamido-1,3,4,6-tetra-O-acetyl-2-deoxy-β-D-glucopyranose 
• 3006-60-8 Acetic acid (2R,3R,4R,5S,6R)-2,5-diacetoxy-6-acetoxymethyl-3-acetylamino-tetrahydro-pyran-4-yl ester 
• 172847-90-4 p-methylphenyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside 
• 10022-13-6 1,3,4,6-tetra-O-acetyl-2-deoxy-2-phthalimido-D-glucopyranose 
• 1276031-05-0 p-methylphenyl 2-deoxy-2-[acetyl(naphthalen-2ylmethyl)amino]-1-thio-β-D-glucopyranoside 
• 1276031-25-4 ethyl 3,4,6-tri-O-acetyl-2-deoxy-2-[acetyl(2,4,6-trimethoxybenzyl)amino]-β-D-glucopyranoside 
• 108-24-7 acetic anhydride 
• 1276031-24-3 p-methylphenyl 3,4,6-tri-O-acetyl-2-deoxy-2-[acetyl(2,4,6-trimethoxybenzyl)amino]-1-thio-β-D-glucopyranoside 
• 1276031-23-2 p-methylphenyl 2-deoxy-2-(2,4,6-trimethoxybenzylamino)-1-thio-β-D-glucopyranoside 
• 1276031-22-1 ethyl 3,4,6-tri-O-acetyl-2-deoxy-2-[acetyl(3,4-dimethoxybenzyl)amino]-β-D-glucopyranoside 
• 1276031-20-9 p-methylphenyl 3,4,6-tri-O-acetyl-2-deoxy-2-[acetyl(3,4-dimethoxybenzyl)amino]-1-thio-β-D-glucopyranoside 
• 1276031-19-6 p-methylphenyl 2-deoxy-2-(3,4-dimethoxybenzylamino)-1-thio-β-D-glucopyranoside 
• 1276031-17-4 ethyl 3,4,6-tri-O-acetyl-2-deoxy-2-[acetyl(4-methoxybenzyl)amino]-β-D-glucopyranoside 

Downstream Products

• 2495-96-7 ethyl N-acetyl-β-glucosaminide 

Relevant articles and documents

Comparing the use of 2-methylenenapthyl, 4-methoxybenzyl, 3,4-dimethoxybenzyl and 2,4,6-trimethoxybenzyl as N-H protecting groups for p-tolyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-1-thio-β-d-glucosides

A hurdle in glycosylation reactions of 2-acetamido glycosyl donors is the formation of a stable and unreactive oxazoline that decreases the yield of these reactions significantly. As an effort to prevent oxazoline formation during glycosylation reactions,

Discovery of the chemical function of glycosidases: Design, synthesis, and evaluation of mass-differentiated carbohydrate libraries

Equation presented. Discovery of the catalytic chemical function of the many putative glycosidases coded in genomes currently relies on individual testing of possible substrates, usually as their p-nitrophenol conjugate. Herein, we present an alternative chemical proteomics approach using a synthetic mass-differentiated heat-stable substrate library with mass spectrometry readout. Library components do not serve as reaction inhibitors and both primary and secondary enzyme substrates can be delineated.