3872-23-9 Usage
Description
Copper Trifluoromethylthiomethanethiol, also known as Copper(I) Trifluoromethanethiolate, is a chemical compound that consists of copper and trifluoromethylthiomethanethiol. It is a significant reagent in the field of organic synthesis due to its unique properties and ability to form various complex structures.
Uses
Used in Pharmaceutical Industry:
Copper Trifluoromethylthiomethanethiol is used as a synthetic reagent for the production of (trifluoromethylthiomethyl/trifluoromethylsulfonylmethyl)dihydropyrazoles. These dihydropyrazoles are important intermediates in the synthesis of various pharmaceutical compounds, including those with potential applications in the treatment of various diseases and disorders.
Used in Chemical Research:
In the field of chemical research, Copper Trifluoromethylthiomethanethiol is utilized as a key building block for the development of novel organic compounds with potential applications in various industries, such as pharmaceuticals, agrochemicals, and materials science. Its unique properties allow for the creation of complex molecular structures that can be further explored for their potential uses and benefits.
Used in Material Science:
Copper Trifluoromethylthiomethanethiol can also be employed in the development of new materials with specific properties, such as improved stability, reactivity, or selectivity. These materials can be used in various applications, including catalysts, sensors, and advanced materials for energy storage and conversion.
Check Digit Verification of cas no
The CAS Registry Mumber 3872-23-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,7 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3872-23:
(6*3)+(5*8)+(4*7)+(3*2)+(2*2)+(1*3)=99
99 % 10 = 9
So 3872-23-9 is a valid CAS Registry Number.
InChI:InChI=1/CHF3S.Cu/c2-1(3,4)5;/h5H;/q;+1/p-1/rCCuF3S/c2-6-1(3,4)5
3872-23-9Relevant articles and documents
Trifluoromethylthiolation of Unsymmetrical λ3-Iodane Derivatives: Additive-Free, Selective and Scalable Introduction of the SCF3 Group
Nikolaienko, Pavlo,Yildiz, Tülay,Rueping, Magnus
supporting information, p. 1091 - 1094 (2016/03/05)
The reaction of copper trifluoromethyl sulfide with diaryliodonium salts provides a straightforward pathway for the synthesis of aryl trifluoromethyl thioethers under mild reaction conditions and within short reaction times. High chemoselectivity was achieved by using mesityl as a leaving group. A large range of novel [(het)aryl](mesityl)iodonium salts underwent this reaction under the optimized conditions to give the desired products in moderate to good yields.
Direct trifluoromethylthiolation of alcohols under mild reaction conditions: Conversion of R-OH into R-SCF3
Nikolaienko, Pavlo,Pluta, Roman,Rueping, Magnus
supporting information, p. 9867 - 9870 (2014/08/18)
A direct process for the trifluoromethylthiolation of allylic and benzylic alcohols under mild conditions has been developed. A wide range of free alcohols underwent nucleophilic substitution in the presence of stable CuSCF3 and BF3·Et2O to give the corresponding products in good to excellent yields.
