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2,6-DIMETHOXYBENZOYLACETONITRILE, a chemical compound with the molecular formula C11H11NO3, is a white crystalline powder. It is a nitrile derivative characterized by the presence of two methoxy groups and a benzoyl group attached to an acetonitrile moiety. 2,6-DIMETHOXYBENZOYLACETONITRILE is widely recognized for its role as an intermediate in the synthesis of pharmaceuticals and agrochemicals, and it also serves as a building block in organic synthesis for creating a variety of other compounds. Moreover, 2,6-DIMETHOXYBENZOYLACETONITRILE has garnered interest due to its potential pharmacological properties, such as antifungal and anticancer activities, highlighting its significance in both industrial and medicinal realms.

847951-47-7

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847951-47-7 Usage

Uses

Used in Pharmaceutical Synthesis:
2,6-DIMETHOXYBENZOYLACETONITRILE is used as an intermediate in the pharmaceutical industry for the synthesis of various drugs. Its unique structure allows it to be a key component in the development of new medicinal compounds, contributing to the advancement of treatments for different health conditions.
Used in Agrochemical Production:
In the agrochemical sector, 2,6-DIMETHOXYBENZOYLACETONITRILE is utilized as an intermediate in the production of pesticides and other agricultural chemicals. Its incorporation aids in enhancing the effectiveness of these products, thereby supporting agricultural productivity and crop protection.
Used in Organic Synthesis:
2,6-DIMETHOXYBENZOYLACETONITRILE is employed as a building block in organic synthesis, enabling the creation of a diverse range of chemical compounds. Its versatility in forming different chemical structures makes it valuable for research and development in the field of organic chemistry.
Used in Antifungal Applications:
2,6-DIMETHOXYBENZOYLACETONITRILE has been studied for its antifungal properties, making it a potential candidate for use in applications aimed at controlling fungal infections. Its effectiveness against fungi could be harnessed in various settings, such as in medical treatments or in preserving materials prone to fungal degradation.
Used in Anticancer Research:
2,6-DIMETHOXYBENZOYLACETONITRILE is also being investigated for its potential anticancer activities. 2,6-DIMETHOXYBENZOYLACETONITRILE is studied as a possible therapeutic agent in oncology, with the aim of developing new strategies to combat cancer and improve patient outcomes.

Check Digit Verification of cas no

The CAS Registry Mumber 847951-47-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,7,9,5 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 847951-47:
(8*8)+(7*4)+(6*7)+(5*9)+(4*5)+(3*1)+(2*4)+(1*7)=217
217 % 10 = 7
So 847951-47-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H11NO3/c1-14-9-4-3-5-10(15-2)11(9)8(13)6-7-12/h3-5H,6H2,1-2H3

847951-47-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2,6-dimethoxyphenyl)-3-oxopropanenitrile

1.2 Other means of identification

Product number -
Other names Benzenepropanenitrile,2,6-dimethoxy-b-oxo

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:847951-47-7 SDS

847951-47-7Downstream Products

847951-47-7Relevant academic research and scientific papers

An improved palladium(II)-catalyzed method for the synthesis of aryl ketones from aryl carboxylic acids and organonitriles

Axelsson, Linda,Veron, Jean-Baptiste,S?vmarker, Jonas,Lindh, Jonas,Odell, Luke R.,Larhed, Mats

supporting information, p. 2376 - 2380 (2014/05/06)

A palladium(II)-catalyzed decarboxylative protocol for the synthesis of aryl ketones has been developed. The addition of TFA was shown to improve the reaction yield and employing THF as solvent enabled the use of solid nitriles and in only a small excess. Using this method, five different benzoic acids reacted with a wide range of nitriles to produce 29 diverse (hetero)aryl ketone derivatives in up to 94% yield.

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