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3,5-DIMETHYL-4-HYDROXYBENZONITRILE, also known as 2,4-dihydroxy-3,5-dimethylbenzonitrile, is an organic nitrile compound with the molecular formula C9H9NO2. It features a benzene ring with two methyl groups and a hydroxy group attached, along with a cyano group. 3,5-DIMETHYL-4-HYDROXYBENZONITRILE is recognized for its potential biological activities, including antioxidant and anti-inflammatory properties, and is widely utilized as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds.

876-15-3

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876-15-3 Usage

Uses

Used in Pharmaceutical Industry:
3,5-DIMETHYL-4-HYDROXYBENZONITRILE is used as a chemical intermediate for the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its presence in these compounds aids in enhancing their efficacy and pharmacological properties.
Used in Agrochemical Industry:
In the agrochemical sector, 3,5-DIMETHYL-4-HYDROXYBENZONITRILE serves as an intermediate in the production of agrochemicals, such as pesticides and herbicides. Its role in these products is crucial for improving their performance and selectivity in agricultural applications.
Used in Organic Synthesis:
3,5-DIMETHYL-4-HYDROXYBENZONITRILE is utilized as a key intermediate in the synthesis of a range of organic compounds. Its unique structure allows for various chemical reactions, making it a valuable component in organic chemistry for creating diverse molecules with specific functions.
Used in Research and Development:
3,5-DIMETHYL-4-HYDROXYBENZONITRILE is also employed in research and development settings for studying its biological activities, such as antioxidant and anti-inflammatory properties. Understanding these properties can lead to the discovery of new applications and uses in medicine and other industries.

Check Digit Verification of cas no

The CAS Registry Mumber 876-15-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,7 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 876-15:
(5*8)+(4*7)+(3*6)+(2*1)+(1*5)=93
93 % 10 = 3
So 876-15-3 is a valid CAS Registry Number.

876-15-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-DIMETHYL-4-HYDROXYBENZONITRILE

1.2 Other means of identification

Product number -
Other names 4-hydroxy-3,5-dimethyl-benzenecarbonitrile

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:876-15-3 SDS

876-15-3Relevant academic research and scientific papers

NOVEL THIOPHENE DERIVATIVES AS IMMUNOSUPPRESSIVE AGENTS

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Page/Page column 36, (2010/02/15)

The invention relates to novel thiophene derivatives, their preparation and their use as pharmaceutically active compounds. Said compounds particularly act as immunosuppressive agents.

NOVEL THIOPHENE DERIVATIVES

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Page/Page column 40-41, (2010/02/15)

The invention relates to novel thiophene derivatives, their preparation and their use as pharmaceutically active compounds. Said compounds particularly act as immunosuppressive agents.

Sulfonamide derivatives for the treatment of diseases

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Page/Page column 34, (2008/06/13)

The invention relates to compounds of formula (1) and to processes for the preparation of, intermediates used in the preparation of, compositions containing and the uses of, such derivatives. The compounds according to the present invention are useful in

Selective copper(II)-mediated oxidative coupling of a nucleophilic reagent to the para-methyl group of 2,4,6-trimethylphenol

Boldron, Christophe,Oezalp-Yaman, Seniz,Gamez, Patrick,Tooke, Duncan M.,Spek, Anthony L.,Reedijk, Jan

, p. 3535 - 3541 (2007/10/03)

A copper(II) neocuproine system has been developed for the efficient and very selective 1,6-addition of a nucleophile to the para-methyl group of 2,4,6-trimethylphenol. Crystallographic and spectroscopic data point towards the involvement of a μ-methoxo-μ-phenoxo-bridged copper species which appears to generate a highly reactive quinone methide intermediate that can be attacked by a nucleophilic reagent. The Royal Society of Chemistry 2005.

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