4-Aminophenyl 2,3,6-tri-O-acetyl-4-O-(2,3,4,6-tetra-O-acetyl-b-D-glucopyranosyl)-b-D-thioglucopyranoside

Base Information

• Chemical Name: 4-Aminophenyl 2,3,6-tri-O-acetyl-4-O-(2,3,4,6-tetra-O-acetyl-b-D-glucopyranosyl)-b-D-thioglucopyranoside
• CAS No.: 68636-50-0
• Molecular Formula: C32H41NO17S
• Molecular Weight: 727.66384
• DSSTox Substance ID: DTXSID801109388
• Mol file: 68636-50-0.mol

Synonyms:68636-50-0;4-Aminophenyl 2,3,6-tri-O-acetyl-4-O-(2,3,4,6-tetra-O-acetyl-b-D-glucopyranosyl)-b-D-thioglucopyranoside;SCHEMBL11050567;MZPWTWYHBZEZSN-CBUXPLGESA-N;DTXSID801109388;W-203262;4-aminophenyl 2,3,6-tri-O-acetyl-4-O-(2,3,4,6-tetra-O-acetyl-beta-D-glucopyranosyl)-1-thio-beta-D-glucopyranoside;beta-D-Glucopyranoside, 4-aminophenyl 4-O-(2,3,4,6-tetra-O-acetyl-beta-D-glucopyranosyl)-1-thio-, 2,3,6-triacetate

Chemical Property of 4-Aminophenyl 2,3,6-tri-O-acetyl-4-O-(2,3,4,6-tetra-O-acetyl-b-D-glucopyranosyl)-b-D-thioglucopyranoside

Chemical Property:

• Vapor Pressure: 0mmHg at 25°C
• Melting Point: 174-176°C
• Boiling Point: 770.568°C at 760 mmHg
• Flash Point: 419.825°C
• PSA: 263.11000
• Density: 1.39g/cm³
• LogP: 1.56180
• Solubility.: Chloroform, Ethyl Acetate
• XLogP3: 0.9
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 19
• Rotatable Bond Count: 20
• Exact Mass: 743.20952001
• Heavy Atom Count: 51
• Complexity: 1270

Purity/Quality:

97% ^*data from raw suppliers

4-Aminophenyl2,3,6-Tri-O-acetyl-4-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-β-D-glucopyranoside ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(=O)OCC1C(C(C(C(O1)OC2C(OC(C(C2OC(=O)C)OC(=O)C)SC3=CC=C(C=C3)N)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C
• Isomeric SMILES: CC(=O)OC[C@@H]1[C@H]([C@@H]([C@H]([C@@H](O1)O[C@@H]2[C@H](O[C@H]([C@@H]([C@H]2OC(=O)C)OC(=O)C)SC3=CC=C(C=C3)N)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C
• Uses: Shown to be a functional affinity ligand for the separation of exo-(cellobiohydrolasees) and endo-(endoglucanases) acting cellulases

Technology Process of 4-Aminophenyl 2,3,6-tri-O-acetyl-4-O-(2,3,4,6-tetra-O-acetyl-b-D-glucopyranosyl)-b-D-thioglucopyranoside

There total 1 articles about 4-Aminophenyl 2,3,6-tri-O-acetyl-4-O-(2,3,4,6-tetra-O-acetyl-b-D-glucopyranosyl)-b-D-thioglucopyranoside 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:

→ 4-Aminophenyl 2,3,6-tri-O-acetyl-4-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-1-thio-β-D-glucopyranoside (68636-50-0)

Guidance literature:

entspr. Glycosylbromid, p-Aminothiophenol;

DOI:10.1016/S0008-6215(00)84136-1

Refernces

• 1、 -. "Poly-cation salt of 4-O-polyhexaose-thio-arylene sulfates". . . Retrieved 2008/06/13.