Glucopyranoside, alpha-cyanobenzyl, D-

Base Information

Chemical Name:Glucopyranoside, alpha-cyanobenzyl, D-
CAS No.:13093-89-5
Molecular Formula:C₁₄H₁₇NO₆
Molecular Weight:295.292
Hs Code.:
DSSTox Substance ID:DTXSID101297403

Synonyms:Glucopyranoside, alpha-cyanobenzyl, D-;SCHEMBL4925774;DTXSID101297403;13093-89-5

Suppliers and Price of Glucopyranoside, alpha-cyanobenzyl, D-

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of Glucopyranoside, alpha-cyanobenzyl, D-

Chemical Property:

XLogP3:-0.7
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:4
Exact Mass:295.10558726
Heavy Atom Count:21
Complexity:377

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(C#N)OC2C(C(C(C(O2)CO)O)O)O
Isomeric SMILES:C1=CC=C(C=C1)C(C#N)OC2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O

Technology Process of Glucopyranoside, alpha-cyanobenzyl, D-

There total 5 articles about Glucopyranoside, alpha-cyanobenzyl, D- 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: 96.0%

: 60981-44-4,60981-47-7,83509-00-6
2-(2,3,4,6-Tetra-O-acetyl-β-D-glucopyranosyloxy)-2-phenylacetonitril

: 13093-89-5
2-(β-D-Glucopyranosyloxy)-2-phenylacetonitril

Guidance literature:: With sodium methylate; In methanol; for 0.25h;

Reference yield:

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

: 13093-89-5
2-(β-D-Glucopyranosyloxy)-2-phenylacetonitril

Guidance literature:: Multi-step reaction with 2 steps

1: 9 percent / HgBr₂/Hg(CN)2 / acetonitrile / 0.07 h / 70 °C

2: 96 percent / NaOCH₃ / methanol / 0.25 h

With sodium methylate; mercury(II) cyanide; mercury dibromide; In methanol; acetonitrile;

Reference yield:

: 532-28-5,613-88-7
(RS)-mandelonitrile

: 13093-89-5
2-(β-D-Glucopyranosyloxy)-2-phenylacetonitril

Guidance literature:: Multi-step reaction with 2 steps

1: 9 percent / HgBr₂/Hg(CN)2 / acetonitrile / 0.07 h / 70 °C

2: 96 percent / NaOCH₃ / methanol / 0.25 h

With sodium methylate; mercury(II) cyanide; mercury dibromide; In methanol; acetonitrile;