327-76-4 Usage
Uses
Used in Pharmaceutical Industry:
2,4-BIS(TRIFLUOROMETHYL)CHLOROBENZENE is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its unique structure and properties contribute to the development of new drugs with specific therapeutic effects.
Used in Agrochemical Industry:
In the agrochemical sector, 2,4-BIS(TRIFLUOROMETHYL)CHLOROBENZENE serves as a precursor in the production of agrochemicals. Its role in creating effective compounds for pest control and crop protection is significant.
Used in Specialty Chemicals Industry:
2,4-BIS(TRIFLUOROMETHYL)CHLOROBENZENE is utilized as a starting material for the synthesis of specialty chemicals. Its versatility in chemical reactions allows for the creation of tailored products for specific applications.
Used as a Precursor for Fluorinated Compounds:
2,4-BIS(TRIFLUOROMETHYL)CHLOROBENZENE is also used as a precursor for the production of other fluorinated compounds. The introduction of fluorine atoms can significantly alter the chemical and physical properties of molecules, leading to a wide range of applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 327-76-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,2 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 327-76:
(5*3)+(4*2)+(3*7)+(2*7)+(1*6)=64
64 % 10 = 4
So 327-76-4 is a valid CAS Registry Number.
327-76-4Relevant academic research and scientific papers
Efficient copper-catalyzed trifluoromethylation of aromatic and heteroaromatic iodides: The beneficial anchoring effect of borates
Gonda, Zsombor,Kovacs, Szabolcs,Weber, Csaba,Gati, Tamas,Meszaros, Attila,Kotschy, Andras,Novak, Zoltan
supporting information, p. 4268 - 4271 (2014/09/30)
Efficient copper-catalyzed trifluoromethylation of aromatic iodides was achieved with TMSCF3 in the presence of trimethylborate. The Lewis acid was used to anchor the in situ generated trifluoromethyl anion and suppress its rapid decomposition. Broad applicability of the new trifluoromethylating reaction was demonstrated in the functionalization of different aromatic and heteroaromatic iodides.