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b-D-Glucopyranoside,2-[[[(2E)-3-(3,4-dihydroxyphenyl)-1-oxo-2-propen-1-yl]oxy]methyl]phenyl is a complex glucopyranoside compound consisting of a glucose molecule attached to a phenyl group with multiple hydroxyl (OH) groups and a propenoyl group. Its molecular structure suggests potential antioxidant and anti-inflammatory properties due to the presence of phenolic groups. b-D-Glucopyranoside,2-[[[(2E)-3-(3,4-dihydroxyphenyl)-1-oxo-2-propen-1-yl]oxy]methyl]phenyl's complex nature indicates possible biological and pharmaceutical applications, although further research is required to fully explore its properties and uses.

26632-35-9

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26632-35-9 Usage

Uses

Used in Pharmaceutical Industry:
b-D-Glucopyranoside,2-[[[(2E)-3-(3,4-dihydroxyphenyl)-1-oxo-2-propen-1-yl]oxy]methyl]phenyl is used as a potential pharmaceutical agent for its possible antioxidant and anti-inflammatory properties, which can be beneficial in the development of treatments for various diseases and conditions.
Used in Cosmetic Industry:
In the cosmetic industry, b-D-Glucopyranoside,2-[[[(2E)-3-(3,4-dihydroxyphenyl)-1-oxo-2-propen-1-yl]oxy]methyl]phenyl may be utilized for its potential antioxidant properties, which can help protect the skin from environmental damage and promote a healthier appearance.
Used in Food Industry:
b-D-Glucopyranoside,2-[[[(2E)-3-(3,4-dihydroxyphenyl)-1-oxo-2-propen-1-yl]oxy]methyl]phenyl could be employed as a natural antioxidant in the food industry to extend the shelf life of products and maintain their quality.
Used in Research:
b-D-Glucopyranoside,2-[[[(2E)-3-(3,4-dihydroxyphenyl)-1-oxo-2-propen-1-yl]oxy]methyl]phenyl is also used in scientific research for studying its potential biological activities and exploring its applications in various fields, including medicine, pharmacology, and biochemistry. Further research is necessary to understand its full potential and optimize its use in different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 26632-35-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,6,3 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 26632-35:
(7*2)+(6*6)+(5*6)+(4*3)+(3*2)+(2*3)+(1*5)=109
109 % 10 = 9
So 26632-35-9 is a valid CAS Registry Number.

26632-35-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name populoside

1.2 Other means of identification

Product number -
Other names (E)-3-(3,4-Dihydroxy-phenyl)-acrylic acid 2-((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-benzyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:26632-35-9 SDS

26632-35-9Downstream Products

26632-35-9Relevant academic research and scientific papers

Synthesis of acyl derivatives of salicin, salirepin, and arbutin

Stepanova, Elena V.,Belyanin, Maxim L.,Filimonov, Victor D.

, p. 105 - 111 (2014/04/03)

The total synthesis of two natural phenolglycosides of the family Salicaceae, namely: populoside and 2-(β-d-glucopyranosyloxy)-5-hydroxy benzyl (3-methoxy-4-hydroxy) cinnamoate and nine not found yet in plants acyl derivatives of phenoglycosides: 2-(β-d-glucopyranosyloxy)-benzylcinnamoate, 2-(β-d-glucopyranosyloxy)-benzyl (4-hydroxy) benzoate, 2-(β-d-glucopyranosyloxy)-benzyl (3-methoxy-4-hydroxy) benzoate, 2-(β-d-glucopyranosyloxy)-5-hydroxy benzyl (3,4-dihydroxy) cinnamoate, 2-(β-d-glucopyranosyloxy)-5-hydroxy benzylcinnamoate, 2-(β-d- glucopyranosyloxy)-5-hydroxy benzyl (4-hydroxy) benzoate, 2-(β-d- glucopyranosyloxy)-5-hydroxy benzyl (3-methoxy-4-hydroxy) benzoate, 2-(β-d-glucopyranosyloxy)-5-benzoyloxy benzylbenzoate and 4-(β-d-glucopyranosyloxy)-phenylbenzoate, starting from readily available phenols and glucose was developed for the first time.

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