106877-34-3 Usage
Uses
Used in Pharmaceutical Industry:
3-Chloro-2-(trifluoromethyl)phenol is used as an intermediate in the synthesis of various pharmaceuticals, contributing to the development of new medications.
Used in Agrochemical Industry:
3-chloro-2-(trifluoromethyl)phenol serves as an intermediate in the production of agrochemicals, aiding in the creation of substances that protect crops and enhance agricultural productivity.
Used as Antimicrobial Agent:
3-Chloro-2-(trifluoromethyl)phenol is utilized as an antimicrobial agent, helping to control microbial growth in various applications.
Used in Production of Surfactants, Solvents, and Catalysts:
It is employed as a raw material in the manufacturing of surfactants, solvents, and catalysts, which are essential in numerous industrial processes.
Used in Materials Science:
3-Chloro-2-(trifluoromethyl)phenol has potential applications in materials science, such as in the production of polymers and coatings, enhancing the properties of these materials.
Safety Note:
3-Chloro-2-(trifluoromethyl)phenol is considered a hazardous substance, and it is crucial to follow proper safety precautions when handling and using this chemical.
Check Digit Verification of cas no
The CAS Registry Mumber 106877-34-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,8,7 and 7 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 106877-34:
(8*1)+(7*0)+(6*6)+(5*8)+(4*7)+(3*7)+(2*3)+(1*4)=143
143 % 10 = 3
So 106877-34-3 is a valid CAS Registry Number.
106877-34-3Relevant articles and documents
Reactions of Trifluoromethyl Bromide and Related Halides: Part 10. Perfluoroalkylation of Aromatic Compounds induced by Sulphur Dioxide Radical Anion Precursors
Tordeux, Marc,Langlois, Bernard,Wakselman, Claude
, p. 2293 - 2299 (2007/10/02)
Perfluoroalkylation of electron-rich aromatic compounds with trifluoromethyl bromide, or long-chain perfluoroalkyl iodides, was performed in the presence of sodium dithionite or zinc-sulphur dioxide.This alkylation occurred at the ortho and para positions relative to the amino or hydroxy substitutent.Pyrroles were perfluoroalkylated regioselectively at the 2-position.This alkylation was interpreted as a radical aromatic substitution; the formation of the perfluoroalkyl radical can be induced by a single-electron transfer from sulphur dioxide radical anion to the perfluoroalkyl halide.
