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2,6-Bis(trifluoromethyl)benzonitrile, with the molecular formula C9H3F6N, is a white crystalline solid characterized by a strong, aromatic odor. It is insoluble in water and is known for its high chemical stability and low reactivity, making it a valuable building block in the synthesis of various compounds. However, it requires careful handling due to its potential harmful effects if ingested, inhaled, or comes into contact with the skin.

25753-25-7

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25753-25-7 Usage

Uses

Used in Pharmaceutical Industry:
2,6-Bis(trifluoromethyl)benzonitrile is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with enhanced properties.
Used in Agrochemical Industry:
In the agrochemical sector, 2,6-Bis(trifluoromethyl)benzonitrile serves as an intermediate, playing a crucial role in the creation of effective pesticides and other agricultural chemicals.
Used in Liquid Crystal Production:
2,6-Bis(trifluoromethyl)benzonitrile is utilized in the production of liquid crystals, which are essential components in display technologies.
Used as a Reagent in Organic Synthesis:
2,6-Bis(trifluoromethyl)benzonitrile is employed as a reagent in organic synthesis, facilitating various chemical reactions and contributing to the synthesis of a wide range of organic compounds.
Used in Specialty Chemicals Manufacturing:
2,6-Bis(trifluoromethyl)benzonitrile is used in the manufacturing of specialty chemicals, where its unique properties are leveraged to produce high-value products for specific applications.

Check Digit Verification of cas no

The CAS Registry Mumber 25753-25-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,7,5 and 3 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 25753-25:
(7*2)+(6*5)+(5*7)+(4*5)+(3*3)+(2*2)+(1*5)=117
117 % 10 = 7
So 25753-25-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H3F6N/c10-8(11,12)6-2-1-3-7(5(6)4-16)9(13,14)15/h1-3H

25753-25-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-BIS(TRIFLUOROMETHYL)BENZONITRILE

1.2 Other means of identification

Product number -
Other names 2,6-Bis-trifluormethyl-benzonitril

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:25753-25-7 SDS

25753-25-7Upstream product

25753-25-7Relevant academic research and scientific papers

Process for producing trifluoromethylbenzylamines

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, (2008/06/13)

The invention relates to a process for producing a trifluotomethylbenzylamine represented by the following general formula (1), 1where each R independently represents a halogen selected from the group consisting of fluorine, chlorine, bromine and iodine, an alkyl group having a carbon atom number of 1-4, an alkoxy group having a carbon atom number of 1-4, an amino group, a hydroxyl group or a trifluoromethyl group, and n represents an integer from 0 to 4. The process includes hydrogenating a trifluoromethylbenzonitrile by hydrogen in an organic solvent in the presence of ammonia and a catalyst containing a platinum group element. This trifluoromethylbenzonitrile is represented by the following general formula (2), 2where R and n are defined as above. With this process, it is possible to obtain the trifluoromethylbenzylamine at an extremely high yield.

Process for producing trifluoromethylbenzylamines

-

, (2008/06/13)

The invention relates to a process for producing a trifluoromethylbenzylamine represented by the following general formula (1). This process includes hydrogenating a trifliuoromethylbenzonitrile represented by the following general formula (2) by hydrogen in an organic solvent in the presence of ammonia, using a Raney catalyst, where each R independently represents a halogen selected from the group consisting of fluorine, chlorine, bromine and iodine, an alkyl group having a carbon atom number of 1-4, an alkoxy group having a carbon atom number of 1-4, an amino group, a hydroxyl group or a trifluoromethyl group, and n represents an integer from 0 to 4, where R and n are defined as above. With this process, it is possible to obtain the trifluoromethylbenzylamine easily and inexpensively at an extremely high yield.

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