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3-(5-Methyl-[1,3,4]oxadiazol-2-yl)-phenol is a heterocyclic chemical compound that features a phenol ring with a 5-methyl-[1,3,4]oxadiazol-2-yl group attached to it. 3-(5-Methyl-[1,3,4]oxadiazol-2-yl)-phenol is known for its potential pharmacological applications due to the bioactivity of the oxadiazole ring, which is commonly found in pharmaceuticals and agrochemicals. The presence of the phenolic group also indicates that it may possess antioxidant and antibacterial properties.

79463-11-9

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79463-11-9 Usage

Uses

Used in Pharmaceutical Industry:
3-(5-Methyl-[1,3,4]oxadiazol-2-yl)-phenol is used as a pharmaceutical compound for its potential bioactivity, which can be harnessed for the development of new drugs. The oxadiazole ring contributes to its potential therapeutic applications, and further research is needed to explore its full medicinal potential.
Used in Agrochemical Industry:
In the agrochemical industry, 3-(5-Methyl-[1,3,4]oxadiazol-2-yl)-phenol is used for its potential as an active ingredient in pesticides or other agrochemical products. The bioactivity of the oxadiazole ring makes it a candidate for further exploration in this field.
Used in Antioxidant Applications:
3-(5-Methyl-[1,3,4]oxadiazol-2-yl)-phenol is used as an antioxidant due to the presence of the phenolic group, which may provide protection against oxidative stress and free radicals.
Used in Antibacterial Applications:
3-(5-Methyl-[1,3,4]oxadiazol-2-yl)-phenol is also used as an antibacterial agent, leveraging the phenolic group's ability to inhibit bacterial growth, which can be beneficial in various medical and industrial settings.
Further research and testing are necessary to determine the full range of potential uses and properties of 3-(5-Methyl-[1,3,4]oxadiazol-2-yl)-phenol, as its current applications are based on its chemical structure and known properties of similar compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 79463-11-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,4,6 and 3 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 79463-11:
(7*7)+(6*9)+(5*4)+(4*6)+(3*3)+(2*1)+(1*1)=159
159 % 10 = 9
So 79463-11-9 is a valid CAS Registry Number.

79463-11-9SDS

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 3-(5-methyl-1,3,4-oxadiazol-2-yl)phenol

1.2 Other means of identification

Product number -
Other names Phenol,3-(5-methyl-1,3,4-oxadiazol-2-yl)

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:79463-11-9 SDS

79463-11-9Relevant articles and documents

SUBSTITUTED CYCLOPROPYL COMPOUNDS, COMPOSITIONS CONTAINING SUCH COMPOUNDS AND METHODS OF TREATMENT

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, (2009/12/02)

Substituted cyclopropyl compounds of formula (I) are disclosed as useful for treating or preventing type 2 diabetes and similar conditions. Pharmaceutically acceptable salts and solvates are included as well. The compounds are useful as agonists of the g-protein coupled receptor GPR-119.

Substituted thieno[3,2-C]pyridine carboxylic acid derivatives

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Page/Page column 9, (2008/06/13)

There are provided compounds of the formula wherein R1, R2, R3, X, ring A and ring B are as described. The compounds exhibit anticancer properties.

Compounds enhancing antitumor activity of other cytotoxic agents

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, (2008/06/13)

This invention relates to certain heterocyclic compounds and their pharmaceutically acceptable salts, which are useful for sensitizing multidrug-resistant tumor cells to anticancer agents and multidrug resistant forms of malaria, tuberculosis, leishmania and amoebic dysentery to chemotherapeutants. The compounds and their pharmaceutically acceptable salts are also inhibitors of the active drug transport capability of P-glycoprotein which is encoded by the human MDR1 gene, as well as of certain other related ATP-binding-cassette transporters from eukaryotic and prokaryotic organisms (e.g., pfmdr from Plasmodium falciprum, and murine mdr1 and mdr3 gene products).

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