106877-34-3 Usage
General Description
3-Chloro-2-(trifluoromethyl)phenol is a chemical compound with the molecular formula C7H4ClF3O. It is an aromatic organic compound with a phenolic structure and a chlorine atom substituted at the 3-position of the phenol ring, as well as a trifluoromethyl group at the 2-position. 3-chloro-2-(trifluoromethyl)phenol is commonly used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. It is also utilized as an antimicrobial agent and as a raw material in the production of surfactants, solvents, and catalysts. Additionally, it has potential applications in the field of materials science, such as in the production of polymers and coatings.3-Chloro-2-(trifluoromethyl)phenol is considered to be a hazardous substance and proper safety precautions should be taken 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.
