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3-(TRIFLUOROMETHYL)PHENOXYACETONITRILE, with the molecular formula C9H6F3NO, is a nitrile derivative featuring a trifluoromethyl group and a phenoxy group. It is recognized for its high reactivity and versatility in organic synthesis, serving as a valuable building block in the creation of a wide range of chemical products. Due to its potentially hazardous nature, it requires careful handling and storage.

2145-31-5

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2145-31-5 Usage

Uses

Used in Pharmaceutical Industry:
3-(TRIFLUOROMETHYL)PHENOXYACETONITRILE is used as a synthetic intermediate for the development of various pharmaceuticals. Its unique structure and reactivity contribute to the synthesis of new drug molecules, enhancing the therapeutic potential of medications.
Used in Agrochemical Industry:
In the agrochemical sector, 3-(TRIFLUOROMETHYL)PHENOXYACETONITRILE is utilized as a precursor in the production of agrochemicals. Its incorporation into these compounds can improve the effectiveness of pesticides and other agricultural products, contributing to more efficient crop protection.
Used in Organic Synthesis:
3-(TRIFLUOROMETHYL)PHENOXYACETONITRILE is employed as a versatile building block in organic synthesis. Its high reactivity allows for the creation of diverse organic compounds, expanding the scope of chemical research and product development.

Check Digit Verification of cas no

The CAS Registry Mumber 2145-31-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,4 and 5 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2145-31:
(6*2)+(5*1)+(4*4)+(3*5)+(2*3)+(1*1)=55
55 % 10 = 5
So 2145-31-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H7FO3/c1-12-8(11)5-2-3-6(9)7(10)4-5/h2-4,10H,1H3

2145-31-5 Well-known Company Product Price

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  • Alfa Aesar

  • (L10794)  3-(Trifluoromethyl)phenoxyacetonitrile, 98%   

  • 2145-31-5

  • 1g

  • 452.0CNY

  • Detail
  • Alfa Aesar

  • (L10794)  3-(Trifluoromethyl)phenoxyacetonitrile, 98%   

  • 2145-31-5

  • 5g

  • 1744.0CNY

  • Detail

2145-31-5SDS

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-[3-(trifluoromethyl)phenoxy]acetonitrile

1.2 Other means of identification

Product number -
Other names 3-(trifluoromethyl)phenoxyacetonitrile

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:2145-31-5 SDS

2145-31-5Relevant academic research and scientific papers

Cytosine analogues from substituted acetonitriles via Thorpe condensation

Barkin, Julia L.,Faust Jr., Marcus D.,Trenkle, William C.

, p. 3333 - 3335 (2007/10/03)

(Matrix presented) A Thorpe condensation is the key bond construction in a rapid and efficient synthesis of substituted cytosine derivatives from readily available starting materials.

Aryloxymethyl imidazolines

-

, (2008/06/13)

The compounds 4[(4,5-dihydro-2-1H-imidazolyl)-methoxy]-N,N,2-trimethylbenzeneamine and 2[(3-trifluoromethylphenoxy)methyl]-2-imidazoline and their pharmaceutically-acceptable salts are described. The compounds are useful as alcohol antagonists in animals

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