beta-D-Glucopyranoside, 5-methyl-3-isoxazolyl

Base Information

Chemical Name:beta-D-Glucopyranoside, 5-methyl-3-isoxazolyl
CAS No.:51937-62-3
Molecular Formula:C10H15NO7
Molecular Weight:261.2286
Hs Code.:
DSSTox Substance ID:DTXSID90199896
Wikidata:Q83072909

Synonyms:beta-D-Glucopyranoside, 5-methyl-3-isoxazolyl;51937-62-3;C10H15NO7;DTXSID90199896

Suppliers and Price of beta-D-Glucopyranoside, 5-methyl-3-isoxazolyl

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of beta-D-Glucopyranoside, 5-methyl-3-isoxazolyl

Chemical Property:

Vapor Pressure:2.64E-12mmHg at 25°C
Boiling Point:535.7°Cat760mmHg
Flash Point:277.8°C
Density:1.547g/cm³
XLogP3:-1.1
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:3
Exact Mass:261.08485182
Heavy Atom Count:18
Complexity:279

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC(=NO1)OC2C(C(C(C(O2)CO)O)O)O
Isomeric SMILES:CC1=CC(=NO1)O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O

Technology Process of beta-D-Glucopyranoside, 5-methyl-3-isoxazolyl

There total 4 articles about beta-D-Glucopyranoside, 5-methyl-3-isoxazolyl 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:

: 52621-68-8
3-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-5-methylisoxazole

: 51937-62-3
3-(β-D-glucopyranosyl)-5-methylisoxazole

Guidance literature:: With methanol; sodium methylate; at 20 ℃; for 1h;

Reference yield:

: 83-87-4,604-68-2,604-69-3,2152-77-4,4026-35-1,4163-59-1,4163-60-4,4163-61-5,4163-65-9,4257-94-7,4257-96-9,16299-15-3,19186-39-1,19189-55-0,25878-60-8,25941-03-1,32445-48-0,32445-49-1,32445-53-7,32445-54-8,34685-58-0,34685-59-1,43168-42-9,43168-44-1,43169-22-8,43169-25-1,66966-07-2,70749-17-6,80184-01-6,93221-01-3,93221-02-4,99630-88-3,109215-53-4,115792-70-6,115792-73-9,139894-92-1,139973-25-4,144071-49-8,147648-81-5
D-glucose pentaacetate

: 51937-62-3
3-(β-D-glucopyranosyl)-5-methylisoxazole

Guidance literature:: Multi-step reaction with 3 steps

1: hydrogen bromide; acetic acid / 1.08 h / 0 - 20 °C

2: potassium carbonate / acetonitrile / 20 h / 20 °C

3: sodium methylate; methanol / 1 h / 20 °C

With methanol; hydrogen bromide; sodium methylate; potassium carbonate; acetic acid; In acetonitrile;

Reference yield:

: 572-09-8
2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide

: 51937-62-3
3-(β-D-glucopyranosyl)-5-methylisoxazole

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / acetonitrile / 20 h / 20 °C

2: sodium methylate; methanol / 1 h / 20 °C

With methanol; sodium methylate; potassium carbonate; In acetonitrile;