6619-04-1

Basic information

• Product Name: α-D-Glucopyranoside, Methyl 2-(acetylaMino)-2-deoxy-4,6-O-(phenylMethylene)-
• Synonyms: α-D-Glucopyranoside, Methyl 2-(acetylaMino)-2-deoxy-4,6-O-(phenylMethylene)-;Methyl 2-acetamido-2-deoxy-4,6-O-benzylidene-alpha-D-glucopyranoside;Methyl 2-acetamido-4,6-O-benzylidene-2-deoxy-alpha-D-glucopyranoside;NSC 75588;1-[4-hydroxy-3-trityloxy-5-(trityloxymethyl)oxolan-2-yl]pyrimidine-2,4-dione
• CAS NO: 6619-04-1
• Molecular Formula: C₁₆H₂₁NO₆
• Molecular Weight: 323.34104
• Mol File: 6619-04-1.mol
• Article Data: 22

Chemical Properties

• Boiling Point: 579.4°Cat760mmHg
• Flash Point: 304.2°C
• Appearance: /
• Density: 1.3g/cm³
• Vapor Pressure: 2.9E-14mmHg at 25°C
• Refractive Index: 1.57
• CAS DataBase Reference: α-D-Glucopyranoside, Methyl 2-(acetylaMino)-2-deoxy-4,6-O-(phenylMethylene)-(CAS DataBase Reference)
• NIST Chemistry Reference: α-D-Glucopyranoside, Methyl 2-(acetylaMino)-2-deoxy-4,6-O-(phenylMethylene)-(6619-04-1)
• EPA Substance Registry System: α-D-Glucopyranoside, Methyl 2-(acetylaMino)-2-deoxy-4,6-O-(phenylMethylene)-(6619-04-1)

Safety Data

• Hazardous Substances Data: 6619-04-1(Hazardous Substances Data)

Usage

General Description

α-D-Glucopyranoside, Methyl 2-(acetylaMino)-2-deoxy-4,6-O-(phenylMethylene)- is a chemical compound composed of a sugar molecule, specifically glucopyranoside, with attached methyl, acetylaMino, and phenylMethylene groups. The presence of the acetylaMino and phenylMethylene groups suggests that this compound may have potential applications in the field of medicinal chemistry, particularly in the development of pharmaceuticals or bioactive compounds. Its unique molecular structure and potential biological activity make it an interesting compound for further study and potential applications in drug development or other areas of chemical research.

InChI:InChI=1/C16H21NO6/c1-9(18)17-12-13(19)14-11(22-16(12)20-2)8-21-15(23-14)10-6-4-3-5-7-10/h3-7,11-16,19H,8H2,1-2H3,(H,17,18)

Upstream product

• 22536-08-9 2-acetylamino-O⁴,O⁶-((Ξ)-benzylidene)-2-deoxy-D-glucose 
• 77-78-1 dimethyl sulfate 
• 100-52-7 benzaldehyde 
• 3946-01-8 methyl N-acetyl-β-D-glucosaminide 
• 6082-04-8 methyl 2-acetylamido-2-deoxy-D-glucoside 
• 7512-17-6 N-Acetyl-D-glucosamine 
• 1125-88-8 benzaldehyde dimethyl acetal 
• 3055-46-7 methyl N-acetyl-D-glucosamine 
• 6748-94-3 methyl 2-acetamido-3-O-acetyl-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside 
• 1078691-95-8 (+)-D-glucosamine hydrochloride 
• 10036-64-3 N-acetyl-D-glucosamine 
• 66537-92-6 methyl 2,3-anhydro-4,6-benzylidene-α-D-allopyranoside 
• 67-56-1 methanol 
• 6748-94-3 methyl-[O³-acetyl-2-acetylamino-O⁴,O⁶-((R)-benzylidene)-2-deoxy-α-D-altropyranoside] 

Downstream Products

• 6748-94-3 methyl 2-acetamido-3-O-acetyl-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside 
• 6619-03-0 methyl 2-acetamido-4,6-O-benzylidene-3-O-mesyl-2-deoxy-α-D-glucopyranoside 
• 6619-06-3 methyl-[2-acetylamino-O⁴,O⁶-((Ξ)-benzylidene)-O³-(toluene-4-sulfonyl)-2-deoxy-α-D-glucopyranoside] 
• 10368-82-8 methyl-[2-acetylamino-O⁴,O⁶-((Ξ)-benzylidene)-O³-methyl-2-deoxy-α-D-glucopyranoside] 
• 17327-09-2 Methyl-2-acetamido-2-deoxy-α-D-altropyranosid 
• 139760-27-3 Methyl O-(2,3,4,6-tetra-O-benzyl-β-D-galactopyranosyl)-(1->3)-2-acetamido-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside 
• 139760-23-9 Methyl O-(2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl)-(1->3)-2-acetamido-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside 
• 120489-36-3 methyl 2-acetamido-4,6-O-benzylidene-2-deoxy-3-O-pivaloyl-α-D-glucopyranoside 
• 139894-28-3 methyl 2-acetamido-4,6-O-benzylidene-2-deoxy-3-O-(p-methoxybenzyl)-α-D-glucopyranoside 
• 69892-42-8 methyl 2-acetamido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside 
• 139760-36-4 Methyl O-(2,3,4-tri-O-benzoyl-α-L-rhamnopyranosyl)-(1->2)-O-(3,4,6-tri-O-acetyl-β-D-galactopyranosyl)-(1->3)-2-acetamido-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside 
• 139760-31-9 Methyl O-(2,3,4-tri-O-benzoyl-α-L-rhamnopyranosyl)-(1->2)-O-(3,4,6-tri-O-acetyl-α-D-galactopyranosyl)-(1->3)-2-acetamido-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside 
• 100638-83-3 methyl 2-acetamido-4,6-O-benzylidene-2-deoxy-3-O--α-D-glucopyranoside 
• 40642-89-5 2-((4aR,6S,7R,8R,8aS)-7-Acetylamino-6-methoxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yloxy)-propionic acid 

Relevant articles and documents

Ultrasonication-Assisted Synthesis of a d-Glucosamine-Based β-CD Inclusion Complex and Its Application as an Aqueous Heterogeneous Organocatalytic System

For the first time, an inclusion complex has been crafted between a carbohydrate-based molecule and a β-cyclodextrin (CD) hydrophobic cavity for asymmetric catalytic applications. This novel d-glucosamine-based inclusion compound has been synthesized in h

Ring-Opening Reactions of the N-4-Nosyl Hough-Richardson Aziridine with Nitrogen Nucleophiles

Dinosylated α-d-glucopyranoside was directly transformed into α-d-altropyranosides via in situ formed N-4-nosyl Hough-Richardson aziridine with nitrogen nucleophiles under mild conditions in fair to excellent yields. The scope of the aziridine ring-opening reaction was substantially broadened contrary to the conventional methods introducing solely the azide anion at high temperatures. If necessary, the N-4-nosyl Hough-Richardson aziridine can be isolated by filtration in a very good yield and high purity.

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