Methyl 6-deoxy-6-[(methylcarbamoyl)amino]hexopyranoside

Base Information

• Chemical Name: Methyl 6-deoxy-6-[(methylcarbamoyl)amino]hexopyranoside
• CAS No.: 41110-58-1
• Molecular Formula: C9H18N2O6
• Molecular Weight: 250.249
• NSC Number: 156598
• DSSTox Substance ID: DTXSID90303097

Synonyms:41110-58-1;NSC156598;methyl 6-deoxy-6-[(methylcarbamoyl)amino]hexopyranoside;DTXSID90303097;NSC-156598

Chemical Property of Methyl 6-deoxy-6-[(methylcarbamoyl)amino]hexopyranoside

Chemical Property:

• Vapor Pressure: 3.16E-13mmHg at 25°C
• Boiling Point: 525.2°Cat760mmHg
• Flash Point: 271.5°C
• Density: 1.39g/cm³
• XLogP3: -2.2
• Hydrogen Bond Donor Count: 5
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 3
• Exact Mass: 250.11648630
• Heavy Atom Count: 17
• Complexity: 264

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CNC(=O)NCC1C(C(C(C(O1)OC)O)O)O

Technology Process of Methyl 6-deoxy-6-[(methylcarbamoyl)amino]hexopyranoside

There total 2 articles about Methyl 6-deoxy-6-[(methylcarbamoyl)amino]hexopyranoside which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 96.0%

methyl 2,3,4-tri-O-acetyl-6-deoxy-6-(N'-methylureido)-α-D-glucopyranoside → methyl 6-deoxy-6-(N'-methylureido)-α-D-glucopyranoside (41110-58-1)

Guidance literature:

With sodium methylate; In methanol;

DOI:10.1016/S0008-6215(00)00040-9

Reference yield:

methyl 2,3,4-tri-O-acetyl-6-deoxy-6-(3-methylcarbodiimido)-α-D-glucopyranoside → methyl 6-deoxy-6-(N'-methylureido)-α-D-glucopyranoside (41110-58-1)

Guidance literature:

Multi-step reaction with 2 steps

1: 180 mg / glacial acetic acid; H₂O / toluene / 0.25 h / 20 °C

2: 96 percent / NaOMe / methanol

With water; sodium methylate; acetic acid; In methanol; toluene; 1: Addition / 2: Deacetylation;

DOI:10.1016/S0008-6215(00)00040-9

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