789-96-8 Usage
Uses
Used in Polymer Production:
2-Chloro-5-(Trifluoromethyl)Benzophenone is used as a chemical intermediate for the synthesis of specific types of polymers. Its unique structure contributes to the properties of the resulting polymers, making it a valuable component in this industry.
Used in Dye Production:
In the dye industry, 2-Chloro-5-(Trifluoromethyl)Benzophenone is used as a key component in the formulation of certain dyes. Its chemical structure allows for the creation of dyes with specific color characteristics and properties.
Used in Pharmaceutical Industry:
2-Chloro-5-(Trifluoromethyl)Benzophenone is used as a building block in the development of pharmaceuticals. Its chemical properties make it a suitable candidate for the synthesis of various drug molecules, potentially leading to new treatments and therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 789-96-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,8 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 789-96:
(5*7)+(4*8)+(3*9)+(2*9)+(1*6)=118
118 % 10 = 8
So 789-96-8 is a valid CAS Registry Number.
InChI:InChI=1/C14H8ClF3O/c15-12-7-6-10(14(16,17)18)8-11(12)13(19)9-4-2-1-3-5-9/h1-8H
789-96-8Relevant academic research and scientific papers
Asymmetric Transfer Hydrogenation of Diaryl Ketones with Ethanol Catalyzed by Chiral NCP Pincer Iridium Complexes
Huang, Zheng,Liu, Guixia,Qian, Lu,Tang, Xixia,Wang, Yulei
supporting information, (2022/02/23)
The use of a chiral (NCP)Ir complex as the precatalyst allowed for the discovery of asymmetric transfer hydrogenation of diaryl ketones with ethanol as the hydrogen source and solvent. This reaction was applicable to various ortho-substituted diaryl keontes, affording benzhydrols in good yields and enantioselectivities. This protocol could be carried out in a gram scale under mild reaction conditions. The utility of the catalytic system was highlighted by the synthesis of the key precursor of (S)-neobenodine.
