(R)-(beta-D-Glucopyranosyloxy)(3-hydroxyphenyl)acetonitrile

Base Information

Chemical Name:(R)-(beta-D-Glucopyranosyloxy)(3-hydroxyphenyl)acetonitrile
CAS No.:41753-54-2
Molecular Formula:C14H17 N O7
Molecular Weight:311.291
Hs Code.:
European Community (EC) Number:255-533-3
DSSTox Substance ID:DTXSID10961956
Nikkaji Number:J278.265K
Wikidata:Q82943508
Mol file:41753-54-2.mol

Synonyms:41753-54-2;(R)-(beta-D-Glucopyranosyloxy)(3-hydroxyphenyl)acetonitrile;EINECS 255-533-3;HOLOCALIN;DTXSID10961956;(Hexopyranosyloxy)(3-hydroxyphenyl)acetonitrile

Suppliers and Price of (R)-(beta-D-Glucopyranosyloxy)(3-hydroxyphenyl)acetonitrile

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

American Custom Chemicals Corporation
HOLOCALIN 95.00%
5MG
$ 504.31

Total 4 raw suppliers

Chemical Property of (R)-(beta-D-Glucopyranosyloxy)(3-hydroxyphenyl)acetonitrile

Chemical Property:

Boiling Point:599.6°Cat760mmHg
Flash Point:316.4°C
PSA：143.40000
Density:1.56g/cm³
LogP:-1.22662
XLogP3:-0.9
Hydrogen Bond Donor Count:5
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:4
Exact Mass:311.10050188
Heavy Atom Count:22
Complexity:411

Purity/Quality:

98%Min ^*data from raw suppliers

HOLOCALIN 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of (R)-(beta-D-Glucopyranosyloxy)(3-hydroxyphenyl)acetonitrile

There total 1 articles about (R)-(beta-D-Glucopyranosyloxy)(3-hydroxyphenyl)acetonitrile 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: 68.3%