Methyl 4-(beta-D-glucopyranosyloxy)benzoate

Base Information

Chemical Name:Methyl 4-(beta-D-glucopyranosyloxy)benzoate
CAS No.:75705-24-7
Molecular Formula:C₁₄H₁₈O₈
Molecular Weight:314.292
Hs Code.:
ChEMBL ID:CHEMBL4860775
DSSTox Substance ID:DTXSID901277431
Nikkaji Number:J3.358.446F

Synonyms:CHEMBL4860775;DTXSID901277431;75705-24-7

Suppliers and Price of Methyl 4-(beta-D-glucopyranosyloxy)benzoate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of Methyl 4-(beta-D-glucopyranosyloxy)benzoate

Chemical Property:

XLogP3:-0.5
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:5
Exact Mass:314.10016753
Heavy Atom Count:22
Complexity:368

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COC(=O)C1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O
Isomeric SMILES:COC(=O)C1=CC=C(C=C1)O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O

Technology Process of Methyl 4-(beta-D-glucopyranosyloxy)benzoate

There total 6 articles about Methyl 4-(beta-D-glucopyranosyloxy)benzoate 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: 98.0%

: 74950-95-1
4-(Methoxycarbonyl)phenyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside

: 75705-24-7
benzoic acid p-(β-D-glucopyranosyloxy)-methyl ester

Guidance literature:: With sodium methylate; In methanol; for 2h; Reflux;
DOI:10.1016/j.bmcl.2014.09.042

Reference yield: 34.0%

: 75705-24-7
benzoic acid p-(β-D-glucopyranosyloxy)-methyl ester

Guidance literature:: With methanol; In dichloromethane; for 0.333333h;

With sodium methylate; In dichloromethane;

Reference yield:

: 604-69-3
β-D-glucose pentaacetate

: 75705-24-7
benzoic acid p-(β-D-glucopyranosyloxy)-methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: phosphorus tribromide / acetic acid / 8 h / 40 °C

2: potassium iodide; potassium carbonate / acetonitrile / 6 h / 50 °C

3: sodium methylate / methanol / 2 h / Reflux

With sodium methylate; phosphorus tribromide; potassium carbonate; potassium iodide; In methanol; acetic acid; acetonitrile;
DOI:10.1016/j.bmcl.2014.09.042