Salicylic acid beta-glucoside

Base Information

Chemical Name:Salicylic acid beta-glucoside
CAS No.:10366-91-3
Molecular Formula:C13H16 O8
Molecular Weight:300.265
Hs Code.:
DSSTox Substance ID:DTXSID50902207
Wikidata:Q105268304
Mol file:10366-91-3.mol

Synonyms:salicylic acid beta-glucoside;salicylic acid glucoside

Suppliers and Price of Salicylic acid beta-glucoside

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

TRC
SalicylicAcid2-O-β-D-Glucoside
500mg
$ 1455.00

TRC
SalicylicAcid2-O-β-D-Glucoside
50mg
$ 185.00

Medical Isotopes, Inc.
SalicylicAcid2-O-β-D-Glucoside
1 g
$ 2200.00

Total 11 raw suppliers

Chemical Property of Salicylic acid beta-glucoside

Chemical Property:

Vapor Pressure:7.64E-15mmHg at 25°C
Boiling Point:591.6°Cat760mmHg
PKA:3.34±0.36(Predicted)
Flash Point:226.9°C
PSA：136.68000
Density:1.588g/cm³
LogP:-1.43650
XLogP3:-1.5
Hydrogen Bond Donor Count:5
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:4
Exact Mass:300.08451746
Heavy Atom Count:21
Complexity:362

Purity/Quality:

98%,99%, ^*data from raw suppliers

SalicylicAcid2-O-β-D-Glucoside ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C(=C1)C(=O)O)OC2C(C(C(C(O2)CO)O)O)O
Uses Salicylic Acid 2-O-β-D-Glucoside (SAG) is the predominant glycosylated metabolite of Salicylic Acid (S088125); a compound that plays an important role in plants, mostly in the induction of systemic acquired resistance (SAR) against pathogens.

Technology Process of Salicylic acid beta-glucoside

There total 6 articles about Salicylic acid beta-glucoside 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: 94.0%

: 10019-60-0
o-methoxycarbonylphenyl β-D-glucopyranoside

: 10366-91-3
2-hydroxy-3-O-β-D-glucopyranosylbenzoic acid

Guidance literature:: With sodium hydroxide; In methanol; for 3h; Ambient temperature;

Reference yield:

: 7791-66-4
2-methoxycarbonylphenyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside

: 10366-91-3
2-hydroxy-3-O-β-D-glucopyranosylbenzoic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 98.2 percent / sodium methanolate / methanol / Ambient temperature

2: 94 percent / sodium hydroxide / methanol / 3 h / Ambient temperature

With sodium hydroxide; sodium methylate; In methanol;

Reference yield:

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

: 10366-91-3
2-hydroxy-3-O-β-D-glucopyranosylbenzoic acid

Guidance literature:: Multi-step reaction with 3 steps

1: 51.2 percent / silver oxide, quinoline / 20 h / Ambient temperature

2: 98.2 percent / sodium methanolate / methanol / Ambient temperature

3: 94 percent / sodium hydroxide / methanol / 3 h / Ambient temperature

With quinoline; sodium hydroxide; sodium methylate; silver(l) oxide; In methanol;