85289-89-0 Usage
Uses
Used in Pharmaceutical Industry:
1-(2-chloroethyl)-4-(trifluoromethyl)benzene is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its unique molecular structure contributes to the development of new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical industry, 1-(2-chloroethyl)-4-(trifluoromethyl)benzene serves as a chemical intermediate, playing a crucial role in the production of agrochemicals that are essential for enhancing crop protection and yield.
Used in Pesticide Production:
1-(2-chloroethyl)-4-(trifluoromethyl)benzene is also utilized in the manufacturing process of pesticides, which are vital for controlling pests and diseases in agriculture, thereby ensuring food security and crop productivity.
Used in Industrial Chemical Production:
1-(2-chloroethyl)-4-(trifluoromethyl)benzene finds application in the production of other industrial chemicals, highlighting its versatility and importance in the chemical industry. Its unique properties allow for the creation of a wide range of products used across various sectors.
Check Digit Verification of cas no
The CAS Registry Mumber 85289-89-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,2,8 and 9 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 85289-89:
(7*8)+(6*5)+(5*2)+(4*8)+(3*9)+(2*8)+(1*9)=180
180 % 10 = 0
So 85289-89-0 is a valid CAS Registry Number.
85289-89-0Relevant academic research and scientific papers
Longwitz, Lars,Jopp, Stefan,Werner, Thomas
, p. 7863 - 7870 (2019)
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.
