Sachaliside

Base Information

Chemical Name:Sachaliside
CAS No.:132294-76-9
Molecular Formula:C₁₅H₂₀O₇
Molecular Weight:312.32
Hs Code.:
UNII:7WNF6LR591
ChEMBL ID:CHEMBL3581238
Nikkaji Number:J398.273D,J440.223E
Wikidata:Q27268953

Synonyms:Sachaliside;Sachaliside 1;(E)-Triandrin;132294-76-9;Sachaliside, (-)-;UNII-7WNF6LR591;Triandrin;7WNF6LR591;19764-35-3;beta-D-Glucopyranoside, 3-(4-hydroxyphenyl)-2-propenyl, (E)-;beta-D-Glucopyranoside, (2E)-3-(4-hydroxyphenyl)-2-propen-1-yl;(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(E)-3-(4-hydroxyphenyl)prop-2-enoxy]oxane-3,4,5-triol;beta-D-Glucopyranoside, 3-(4-hydroxyphenyl)-2-propen-1-yl;(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-(((E)-3-(4-hydroxyphenyl)allyl)oxy)tetrahydro-2H-pyran-3,4,5-triol;MEGxp0_001501;CHEMBL3581238;CHEBI:181987;AKOS040753896;AKOS040763037;NCGC00385488-01;Q27268953;.BETA.-D-GLUCOPYRANOSIDE, (2E)-3-(4-HYDROXYPHENYL)-2-PROPEN-1-YL;.BETA.-D-GLUCOPYRANOSIDE, 3-(4-HYDROXYPHENYL)-2-PROPENYL, (E)-;NCGC00385488-01_C15H20O7_beta-D-Glucopyranoside, (2E)-3-(4-hydroxyphenyl)-2-propen-1-yl

Suppliers and Price of Sachaliside

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 Sachaliside

Chemical Property:

XLogP3:-0.4
Hydrogen Bond Donor Count:5
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:5
Exact Mass:312.12090297
Heavy Atom Count:22
Complexity:354

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1C=CCOC2C(C(C(C(O2)CO)O)O)O)O
Isomeric SMILES:C1=CC(=CC=C1/C=C/CO[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O)O

Technology Process of Sachaliside

There total 6 articles about Sachaliside 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: 95.0%

: 857500-51-7
4-hydroxycinnamyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside

: 132294-76-9
p-coumaryl alcohol-γ-O-β-D-glucopyranoside

Guidance literature:: With sodium methylate; In methanol;
DOI:10.1016/j.tetlet.2005.04.023

Reference yield: 68.0%

: 20649-40-5
(E)-4-(3-hydroxyprop-1-enyl)phenol

: 153-18-4
rutin

: 132294-76-9
p-coumaryl alcohol-γ-O-β-D-glucopyranoside

Guidance literature:: With α-L-rhamnosyl-β-D-glucosidase from Aspergillus niger; In aq. phosphate buffer; dimethyl sulfoxide; at 35 ℃; for 8h; pH=5; regioselective reaction; Enzymatic reaction;
DOI:10.1002/cssc.201700136

Reference yield:

: 71597-85-8
(p-hydroxyphenyl)boronic acid

: 132294-76-9
p-coumaryl alcohol-γ-O-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 52 percent / copper(II) acetate; lithium acetate; palladium(II) acetate / dimethylformamide / 0.5 h / 80 °C

2: 95 percent / NaOMe / methanol / 0.5 h

With lithium acetate; sodium methylate; copper diacetate; palladium diacetate; In methanol; N,N-dimethyl-formamide; 1: Mizoroki-Heck reaction;
DOI:10.1016/j.tet.2005.08.043