3055-46-7

Basic information

• Product Name: METHYL 2-ACETAMIDO-2-DEOXY-A-D-GALACTOPYRANOSIDE
• Synonyms: METHYL 2-ACETAMIDO-2-DEOXY-A-D-GALACTOPYRANOSIDE;Methyl 2-Acetamido-2-deoxy-b-D-galactopyranoside;Methyl 2-Acetamido-2-deoxy-α-D-galactopyranoside;D-Glucopyranoside, Methyl 2-(acetylaMino)-2-deoxy-
• CAS NO: 3055-46-7
• Molecular Formula: C₉H₁₇NO₆
• Molecular Weight: 235.23438
• Product Categories: 13C & 2H Sugars;Carbohydrates & Derivatives
• Mol File: 3055-46-7.mol
• Article Data: 20

Chemical Properties

• Melting Point: 175-181℃
• Boiling Point: 525.5±50.0 °C(Predicted)
• Appearance: /
• Density: 1.36
• PKA: 12.98±0.70(Predicted)
• CAS DataBase Reference: METHYL 2-ACETAMIDO-2-DEOXY-A-D-GALACTOPYRANOSIDE(CAS DataBase Reference)
• NIST Chemistry Reference: METHYL 2-ACETAMIDO-2-DEOXY-A-D-GALACTOPYRANOSIDE(3055-46-7)
• EPA Substance Registry System: METHYL 2-ACETAMIDO-2-DEOXY-A-D-GALACTOPYRANOSIDE(3055-46-7)

Safety Data

• Hazardous Substances Data: 3055-46-7(Hazardous Substances Data)

Usage

Chemical Properties

White Crystalline Solid

Upstream product

• 67-56-1 methanol 
• 7512-17-6 N-Acetyl-D-glucosamine 
• 10036-64-3 N-acetyl-D-glucosamine 
• 75-36-5 acetyl chloride 
• 1078691-95-8 (+)-D-glucosamine hydrochloride 
• 72-87-7 N-acetyl-D-glucosamine 

Downstream Products

• 88295-36-7 1-O-Methyl-2-N-acetylamino-2-deoxy-4,6-O-benzyliden-α,β-D-glucopyranosid 
• 2771-48-4 methyl 2-acetamido-3,4,6-O-triacetyl-2-deoxy-β-D-glucopyranoside 
• 2595-39-3 methyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-α-D-glucopyranoside 
• 3006-60-8 Acetic acid (2R,3R,4R,5S,6R)-2,5-diacetoxy-6-acetoxymethyl-3-acetylamino-tetrahydro-pyran-4-yl ester 
• 42756-57-0 methyl 2-acetamido-2-deoxy-6-O-trityl-D-glucopyranoside 
• 6619-04-1 N-((4aR,6S,7R,8R,8aS)-8-Hydroxy-6-methoxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl)-acetamide 
• 10300-76-2 methyl 2-acetamido-4,6-O-benzylidene-2-deoxy-β-D-glucopyranoside 
• 87038-18-4 methyl 2-acetylamido-4,6-O-benzylidene-2-deoxy-β-D-glucopyranoside 
• 6619-02-9 methyl N-acetyl-2-amino-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside 
• 154125-86-7 methyl 2-deoxy-3,4,6-tri-O-benzyl-2-(N-acetylamino)-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 
• 4288-74-8 methyl 2-N-acetylamido-4,6-O-benzylidene-2-deoxy-3-ulose-α-D-ribo-hexapyranoside 
• 69892-44-0 methyl 2-acetylamino-3-O-benzyl-2-deoxy-α-D-glucopyranoside 

Relevant articles and documents

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

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Sugar derived alkamine catalytic imine reduction method

The invention discloses a method used for catalytic reduction of imine with saccharide-derivatized amino alcohol. According to the method, imine is taken as a substrate. The method comprises following steps: 1) imine and saccharide-derivatized amino alcohol are dissolved in an organic solvent I, wherein molar ratio of imine to saccharide-derivatized amino alcohol ranges from 100:1-20; 2) trichlorosilane with 1.5 to 5 times equivalent weights is added into a solution obtained via step 1) dropwise, an obtained mixture is stirred and reacted for 12 to 36h at a temperature of -20 to 40 DEG C, and a saturated sodium bicarbonate solution is used for quenching; 3) a material obtained via step 2) is extracted with an organic solvent II, and is subjected to column chromatography isolation so as to obtain amine compounds.