GlcNPhth[36Bn,4Ac]-beta-MP

Base Information

• Chemical Name: GlcNPhth[36Bn,4Ac]-beta-MP
• CAS No.: 140615-77-6
• Molecular Formula: C37H35NO9
• Molecular Weight: 637.682
• DSSTox Substance ID: DTXSID60693674
• Mol file: 140615-77-6.mol

Synonyms:GlcNPhth[36Bn,4Ac]-beta-MP;DTXSID60693674;M1834;4-Methoxyphenyl 4-O-acetyl-3,6-di-O-benzyl-2-deoxy-2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-alpha-L-erythro-hexopyranoside

Chemical Property of GlcNPhth[36Bn,4Ac]-beta-MP

Chemical Property:

• Vapor Pressure: 0mmHg at 25°C
• Boiling Point: 752.944°C at 760 mmHg
• Flash Point: 409.166°C
• PSA: 109.83000
• Density: 1.34g/cm³
• LogP: 5.13550
• Storage Temp.: 0-10°C
• Solubility.: soluble in Chloroform
• XLogP3: 5.2
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 9
• Rotatable Bond Count: 13
• Exact Mass: 637.23118169
• Heavy Atom Count: 47
• Complexity: 1010

Purity/Quality:

97% ^*data from raw suppliers

4-Methoxyphenyl4-O-Acetyl-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(=O)OC1C(OC(C(C1OCC2=CC=CC=C2)N3C(=O)C4=CC=CC=C4C3=O)OC5=CC=C(C=C5)OC)COCC6=CC=CC=C6
• Isomeric SMILES: CC(=O)OC1[C@@H](O[C@H](C([C@H]1OCC2=CC=CC=C2)N3C(=O)C4=CC=CC=C4C3=O)OC5=CC=C(C=C5)OC)COCC6=CC=CC=C6
• Uses: 4-Methoxyphenyl 4-O-Acetyl-3,6-di-O-benzyl-2-deoxy-2-phthalimido-beta-D-glucopyranoside (CAS# 140615-77-6) is a useful building block used in the preparation of chitooligosaccharides as plant growth inhibitors, antimicrobials, and antineoplastics.

Technology Process of GlcNPhth[36Bn,4Ac]-beta-MP

There total 1 articles about GlcNPhth[36Bn,4Ac]-beta-MP 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: 75.0%

p-Methoxyphenyl 3-O-benzyl-4,6-O-benzylidene-2-deoxy-2-phthalimido-β-D-glucopyranoside (129575-88-8) + acetic anhydride (108-24-7) → 4-methoxyphenyl 4-O-acetyl-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside (140615-77-6)

Guidance literature:

p-Methoxyphenyl 3-O-benzyl-4,6-O-benzylidene-2-deoxy-2-phthalimido-β-D-glucopyranoside; With molecular sieve; methanesulfonic acid; sodium cyanoborohydride; In tetrahydrofuran; at 20 ℃; for 2h; pH=2.5 - 3;

acetic anhydride; With pyridine; at 20 ℃; for 18h; Further stages.;

DOI:10.1016/j.carres.2006.10.009

Reference yield:

4-methoxyphenyl 4-O-acetyl-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside (140615-77-6) → p-methoxyphenyl 3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside (129575-89-9)

Guidance literature:

With magnesium methanolate; In tetrahydrofuran; methanol; at 20 ℃; for 2.5h;

DOI:10.1016/j.carres.2006.10.009

upstream raw materials:

p-Methoxyphenyl 3-O-benzyl-4,6-O-benzylidene-2-deoxy-2-phthalimido-β-D-glucopyranoside

acetic anhydride

Downstream raw materials:

p-methoxyphenyl 3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside

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