94022-94-3 Usage
Uses
Used in Pharmaceutical Industry:
1-(2-chloroethyl)-2-(trifluoromethyl)benzene is used as an intermediate for the synthesis of various pharmaceuticals. Its unique structure allows for the creation of a wide range of medicinal compounds, contributing to the development of new drugs and therapies.
Used in Agrochemical Industry:
In the agrochemical sector, 1-(2-chloroethyl)-2-(trifluoromethyl)benzene serves as a crucial intermediate in the production of pesticides and other agricultural chemicals. Its incorporation into these products can enhance their effectiveness in protecting crops and controlling pests.
Used in Specialty Chemicals:
1-(2-chloroethyl)-2-(trifluoromethyl)benzene is also utilized as a building block for the synthesis of specialty chemicals. These chemicals have specific applications in various industries, such as plastics, coatings, and textiles, where their unique properties are highly valued.
Used as a Solvent:
Due to its chemical properties, 1-(2-chloroethyl)-2-(trifluoromethyl)benzene can be employed as a solvent in certain chemical processes. Its ability to dissolve a range of substances makes it a valuable asset in the chemical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 94022-94-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,0,2 and 2 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 94022-94:
(7*9)+(6*4)+(5*0)+(4*2)+(3*2)+(2*9)+(1*4)=123
123 % 10 = 3
So 94022-94-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H8ClF3/c10-6-5-7-3-1-2-4-8(7)9(11,12)13/h1-4H,5-6H2
94022-94-3Relevant academic research and scientific papers
Organocatalytic Chlorination of Alcohols by P(III)/P(V) Redox Cycling
Longwitz, Lars,Jopp, Stefan,Werner, Thomas
, p. 7863 - 7870 (2019/06/27)
A catalytic system for the chlorination of alcohols under Appel conditions was developed. Benzotrichloride is used as a cheap and readily available chlorinating agent in combination with trioctylphosphane as the catalyst and phenylsilane as the terminal reductant. The reaction has several advantages over other variants of the Appel reaction, e.g., no additional solvent is required and the phosphane reagent is used only in catalytic amounts. In total, 27 different primary, secondary, and tertiary alkyl chlorides were synthesized in yields up to 95%. Under optimized conditions, it was also possible to convert epoxides and an oxetane to the dichlorinated products.
