135130-97-1 Usage
Description
2,4,6-Tris(trifluoromethyl)benzoyl Chloride is an organic compound characterized by its trifluoromethyl groups and benzoyl chloride structure. It serves as a crucial intermediate in the synthesis of various fluorinated compounds, which have significant applications in the medical and chemical industries.
Uses
Used in Pharmaceutical Industry:
2,4,6-Tris(trifluoromethyl)benzoyl Chloride is used as an intermediate for the synthesis of 2,4,6-Tris(trifluoromethyl)aniline (T876695), which is a fluorinated compound with valuable applications in medical chemistry. The presence of fluorinated substituents in this compound enhances its properties, making it a promising candidate for the development of new drugs and therapeutic agents.
Used in Chemical Industry:
In the chemical industry, 2,4,6-Tris(trifluoromethyl)benzoyl Chloride is utilized for the preparation of azo dyes containing fluorine. These dyes are important for various applications, including the production of pigments, inks, and coatings. The incorporation of fluorine into these dyes improves their stability, color intensity, and resistance to environmental factors, making them more suitable for a wide range of uses.
Check Digit Verification of cas no
The CAS Registry Mumber 135130-97-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,1,3 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 135130-97:
(8*1)+(7*3)+(6*5)+(5*1)+(4*3)+(3*0)+(2*9)+(1*7)=101
101 % 10 = 1
So 135130-97-1 is a valid CAS Registry Number.
135130-97-1Relevant articles and documents
Preparation and reactions of 2,4,6-tris(trifluoromethyl)phenylamine
Ahlemann, Jens-T,Roesky, Herbert W.,Noltemeyer, Mathias,Schmidt, Hans-G.,Markovsky, Leonid N.,Shermolovich, Yuri G.
, p. 87 - 90 (2007/10/03)
Starting from RfH (1) [Rf = 1,3,5-tris(trifluoromethyl)phenyl] RfNH2 (6) is obtained in a four-step synthesis. The amine 6 reacts with chlorotrimethylsilane in the presence of DBU (1,8-diazabicyclo(5,4,0)undec-7
