1060802-11-0 Usage
Description
1-(5-chloropyridin-3-yl)-2,2,2-trifluoroethanone is a chemical compound characterized by the presence of a 5-chloropyridin-3-yl group attached to a 2,2,2-trifluoroethanone moiety. It is recognized for its strong electron-withdrawing properties due to the trifluoromethyl group, which contributes to its unique structure and reactivity. 1-(5-chloropyridin-3-yl)-2,2,2-trifluoroethanone serves as a valuable building block in organic synthesis and pharmaceutical research, playing a crucial role in the development of biologically active molecules.
Uses
Used in Organic Synthesis:
1-(5-chloropyridin-3-yl)-2,2,2-trifluoroethanone is used as a building block in organic synthesis for the creation of various organic compounds. Its strong electron-withdrawing properties make it a versatile component in the synthesis of complex organic molecules.
Used in Pharmaceutical Research:
In Pharmaceutical Research, 1-(5-chloropyridin-3-yl)-2,2,2-trifluoroethanone is used as an intermediate for the development of biologically active molecules. Its unique structure and reactivity are instrumental in the production of pharmaceuticals, contributing to the discovery and synthesis of new drugs.
Used in Agrochemicals:
1-(5-chloropyridin-3-yl)-2,2,2-trifluoroethanone is utilized as a key intermediate in the agrochemical industry for the synthesis of active ingredients in pesticides and other agricultural chemicals, enhancing the effectiveness of these products.
Used in Materials Science:
In Materials Science, 1-(5-chloropyridin-3-yl)-2,2,2-trifluoroethanone is employed in the development of new materials with specific properties, such as high thermal stability or unique electronic characteristics, due to its strong electron-withdrawing nature.
Used in Chemical Industry:
1-(5-chloropyridin-3-yl)-2,2,2-trifluoroethanone is broadly applied across the chemical industry as an important intermediate for the production of a wide range of chemical products, leveraging its electron-withdrawing properties and reactivity in various chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 1060802-11-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,6,0,8,0 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1060802-11:
(9*1)+(8*0)+(7*6)+(6*0)+(5*8)+(4*0)+(3*2)+(2*1)+(1*1)=100
100 % 10 = 0
So 1060802-11-0 is a valid CAS Registry Number.
1060802-11-0Relevant articles and documents
Preparation method of 3H bis-aziridinyl disubstituted pyridine derivative
-
Paragraph 0020; 0021; 0026; 0027; 0032; 0033; 0038; 0039, (2019/01/16)
A preparation method of a 3H bis-aziridinyl disubstituted pyridine derivative includes utilizing 3-chloro-5-bromopyridine, anhydrous diethyl ether, n-butyl lithium and ethyl trifluoroacetate as raw materials to have reaction to obtain 1-(5-chloropyridine-
