10300-76-2

Basic information

• Product Name: Methyl2-acetamido-4,6-O-benzylidene-2-deoxy-b-D-glucopyranoside
• Synonyms: Methyl2-acetamido-4,6-O-benzylidene-2-deoxy-b-D-glucopyranoside;Methyl 2-(AcetylaMino)-2-deoxy-4,6-O-(phenylMethylene)-β-D-glucopyranoside
• CAS NO: 10300-76-2
• Molecular Formula: C₁₆H₂₁NO₆
• Molecular Weight: 323.34
• Product Categories: Carbohydrates & Derivatives
• Mol File: 10300-76-2.mol
• Article Data: 18

Chemical Properties

• Melting Point: 296-298 °C
• Boiling Point: 579.4±50.0 °C(Predicted)
• Appearance: /
• Density: 1.30±0.1 g/cm3(Predicted)
• PKA: 12.70±0.70(Predicted)
• CAS DataBase Reference: Methyl2-acetamido-4,6-O-benzylidene-2-deoxy-b-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: Methyl2-acetamido-4,6-O-benzylidene-2-deoxy-b-D-glucopyranoside(10300-76-2)
• EPA Substance Registry System: Methyl2-acetamido-4,6-O-benzylidene-2-deoxy-b-D-glucopyranoside(10300-76-2)

Safety Data

• Hazardous Substances Data: 10300-76-2(Hazardous Substances Data)

Usage

Description

Methyl2-acetamido-4,6-O-benzylidene-2-deoxy-b-D-glucopyranoside, with the CAS number 10300-76-2, is a complex organic compound that plays a significant role in the field of organic synthesis. It is a derivative of a sugar molecule, specifically a glucopyranoside, with a benzylidene group and an acetamido group attached to it. This unique structure endows it with potential applications in various industries.

Uses

Used in Organic Synthesis:
Methyl2-acetamido-4,6-O-benzylidene-2-deoxy-b-D-glucopyranoside is used as a key intermediate in the synthesis of various complex organic molecules. Its unique structure allows for the creation of a wide range of compounds with diverse properties and applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Methyl2-acetamido-4,6-O-benzylidene-2-deoxy-b-D-glucopyranoside is used as a building block for the development of new drugs. Its structural versatility enables the design of molecules with specific biological activities, making it a valuable asset in drug discovery and development.
Used in Chemical Research:
Methyl2-acetamido-4,6-O-benzylidene-2-deoxy-b-D-glucopyranoside is also utilized in chemical research to study the properties and reactivity of complex organic molecules. Its unique structure provides insights into the behavior of similar compounds and contributes to the advancement of organic chemistry.
Used in Material Science:
In the field of material science, Methyl2-acetamido-4,6-O-benzylidene-2-deoxy-b-D-glucopyranoside can be used to develop novel materials with specific properties. Its incorporation into polymers or other materials can lead to the creation of materials with enhanced characteristics, such as improved stability or biocompatibility.

Upstream product

• 22536-08-9 2-acetylamino-O⁴,O⁶-((Ξ)-benzylidene)-2-deoxy-D-glucose 
• 77-78-1 dimethyl sulfate 
• 7512-17-6 N-Acetyl-D-glucosamine 
• 1125-88-8 benzaldehyde dimethyl acetal 
• 76899-76-8 1-O-Methyl-2-amino-2-deoxy-4,6-O-benzyliden-β-D-glucopyranosid 
• 108-24-7 acetic anhydride 
• 3055-46-7 methyl N-acetyl-D-glucosamine 
• 100-52-7 benzaldehyde 
• 3946-01-8 methyl N-acetyl-β-D-glucosaminide 
• 6082-04-8 methyl 2-acetylamido-2-deoxy-D-glucoside 
• 14131-63-6 D-glucosamine hydrochloride 
• 14131-68-1 N-acetyl-D-glucosamine 
• 22854-00-8 2-methyl-(1,2-dideoxy-α-D-glucopyranoso)-[2,1-d]-2-oxazoline 
• 66537-92-6 methyl 2,3-anhydro-4,6-benzylidene-α-D-allopyranoside 

Downstream Products

• 139894-30-7 methyl-[O³-acetyl-2-acetylamino-O⁴,O⁶-((Ξ)-benzylidene)-2-deoxy-β-D-glucopyranoside] 
• 17327-09-2 Methyl-2-acetamido-2-deoxy-α-D-altropyranosid 
• 162427-96-5 methyl O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-(1<*>3)-2-acetamido-4,6-O-benzylidene-2-deoxy-β-D-glucopyranoside 
• 142756-66-9 methyl 2-acetamido-3-O-(2-O-acetyl-3,4-di-O-benzyl-6-O-methyl-β-D-galactopyranosyl)-4,6-O-benzylidene-2-deoxy-β-D-glucopyranoside 
• 100638-83-3 methyl 2-acetamido-4,6-O-benzylidene-2-deoxy-3-O--α-D-glucopyranoside 
• 260970-14-7 methyl 2,3-di-O-benzoyl-4,6-dideoxy-α-L-lyxo-hexopyranosyl-(1->3)-2-acetamido-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside 
• 260970-15-8 methyl 2-O-benzoyl-3-O-benzyl-4-deoxy-4-fluoro-α-L-rhamnopyranosyl-(1->3)-2-acetamido-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside 
• 311778-92-4 methyl (2,3,4-tri-O-benzoyl-α-L-rhamnopyranosyl)-(1->3)-2-acetamido-2-deoxy-4,6-O-benzylidene-β-D-glucopyranoside 
• 354986-48-4 methyl 2-acetamido-4,6-O-benzylidene-2-deoxy-3-O-(2-picolinyl)-α-D-glucopyranoside 
• 144789-65-1 methyl 2-acetamido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside 
• 354986-45-1 methyl N-acetyl-N-benzyl-2-amino-2-deoxy-3-O-benzyl-4,6-O-benzylidene-α-D-glucopyranoside 
• 651736-01-5 methyl 2-amino-4,6-O-benzylidene-2-deoxy-α-D-allopyranoside 
• 78216-83-8 methyl 2-acetylamido-4,6-O-benzylidene-2-deoxy-α-D-allopyranoside 
• 85193-92-6 methyl 2-acetamido-3,6-di-O-benzyl-2-deoxy-α-D-glucopyranoside 

Relevant articles and documents

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D-Glucosamine as a novel chiral auxiliary for the stereoselective synthesis of P-stereogenic phosphine oxides

D-Glucosamine was successfully employed as a chiral auxiliary for the enantioselective synthesis of phosphine oxides. The influence of the anomeric position was also investigated and revealed the excellent ability of the α-anomer to perform this transform

3- and 4-uloses derived from N-acetyl- D -glucosamine: A unique pair of complementary organocatalysts for asymmetric epoxidation of alkenes

The 4-ulose and the 3-ulose, both derived in two steps from the α-methyl glycoside of N-acetyl-D-glucosamine (GlcNAc), act as organocatalysts in the asymmetric epoxidation of alkenes, with unprecedented complementary enantioselectivity. The best results are found with α,β-unsaturated esters as substrates, with enantiomeric ratios up to 90:10 and 11:89, respectively. Copyright