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1,2-Benzenediol, 3-(2-pyridinylmethyl)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

756900-93-3

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756900-93-3 Usage

Structure

A benzene ring with two hydroxyl groups and a pyridine ring attached to one of the carbon atoms in the benzene ring.

Pharmaceutical Industry

Used for its antioxidant properties.

Cosmetic Industry

Added to skincare products for protection against free radicals.

Antioxidant Properties

Protects the skin from damage caused by free radicals.

Research

Ongoing research in the field of medicinal chemistry for potential applications in the development of new drugs for various medical conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 756900-93-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,5,6,9,0 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 756900-93:
(8*7)+(7*5)+(6*6)+(5*9)+(4*0)+(3*0)+(2*9)+(1*3)=193
193 % 10 = 3
So 756900-93-3 is a valid CAS Registry Number.

756900-93-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(pyridin-2-ylmethyl)benzene-1,2-diol

1.2 Other means of identification

Product number -
Other names -

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:756900-93-3 SDS

756900-93-3Upstream product

756900-93-3Downstream Products

756900-93-3Relevant academic research and scientific papers

Synthesis of vicinal diols from various arenes with a heterocyclic, amino or carboxyl group by using recombinant Escherichia coli cells expressing evolved biphenyl dioxygenase and dihydrodiol dehydrogenase genes

Misawa, Norihiko,Nakamura, Ryoko,Kagiyama, Yukiko,Ikenaga, Hiroshi,Furukawa, Kensuke,Shindo, Kazutoshi

, p. 195 - 204 (2005)

Various aromatic molecules, in which heterocycles are linked with a phenyl or benzyl group, were converted to their respective 2,3-diols (catechols) in the benzene ring by growing cell reactions using recombinant Escherichia coli, which expressed the evolved biphenyl dioxygenase [bphA (2072)] genes and the subsequent bacterial dihydrodiol dehydrogenase (bphB) gene. These vicinal diol products showed strong in vitro inhibitory activity against the lipid peroxidation induced by free radicals and strong scavenging activity towards DPPH radicals. The vicinal diols were also synthesized from ionized monocyclic aromatics incorporating an amino or carboxyl group. Graphical abstract.

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