79623-37-3 Usage
Uses
Used in Pharmaceutical Synthesis:
2(3H)-PYRIDINONE, 3-CHLORO-5-(TRIFLUOROMETHYL)is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows it to be a building block for the creation of new medicinal compounds, potentially leading to the development of novel treatments for a range of diseases and conditions.
Used in Agrochemical Production:
In the agrochemical industry, 2(3H)-PYRIDINONE, 3-CHLORO-5-(TRIFLUOROMETHYL)is employed in the production of pesticides and other crop protection agents. Its chemical properties make it a valuable component in the formulation of effective and targeted agrochemicals that can protect crops from pests and diseases.
Used in Medicinal Chemistry Research:
2(3H)-PYRIDINONE, 3-CHLORO-5-(TRIFLUOROMETHYL)is utilized in medicinal chemistry for research purposes. Scientists and researchers use 2(3H)-PYRIDINONE, 3-CHLORO-5-(TRIFLUOROMETHYL)- to explore its potential interactions with biological targets, which can provide insights into the development of new drugs and therapies.
Safety Considerations:
It is crucial to handle 2(3H)-PYRIDINONE, 3-CHLORO-5-(TRIFLUOROMETHYL)with care due to its potential hazards. Proper safety measures should be implemented to minimize risks associated with its use, ensuring the well-being of individuals involved in its synthesis, application, and research.
Check Digit Verification of cas no
The CAS Registry Mumber 79623-37-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,6,2 and 3 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 79623-37:
(7*7)+(6*9)+(5*6)+(4*2)+(3*3)+(2*3)+(1*7)=163
163 % 10 = 3
So 79623-37-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H3ClF3NO/c7-4-1-3(6(8,9)10)2-11-5(4)12/h1-2,4H
79623-37-3Relevant academic research and scientific papers
Alcoholysis of trifluoromethyl groups attached to the pyridine ring
Qian, Xuhong,Liu, Shuyou
, p. 9 - 12 (2007/10/03)
In dimethylformamide solution, trifluoroethoxylation and methoxylation of 5-chloro-3-trifluoromethylpyridine (2) yield 5-chloro-3-tris(trifluoroethoxyl)methyl pyridine (2a) and a dimethyl ketal of 3-chloronicotinic acid anhydride (2b) with fluorines as leaving groups, respectively. The corresponding reactions of 2,3-dichloro-5-trifluoromethylpyridine (3) only yield the 2-alkoxy-substituted products 3a and 3b with chloro as the leaving group and the 2-dimethylamino product 3c which was formed by the action of solvent dimethylformamide as a nucleophile. Differences in their reaction behaviour and possible mechanisms are also discussed.
Trifluoromethyl-2-pyridinone or pyridinthione compounds and process for the preparation of the same
-
, (2008/06/13)
A trifluoromethyl-2-(thio)pyridone compound having the formula: STR1 wherein X represents a hydrogen atom or a halogen atom, Y1 and Y2 each represents a hydrogen atom, a halogen atom or a trifluoromethyl group, and Z represents an oxygen atom or a sulfur atom, in which either Y1 or Y2 represents a trifluoromethyl group, and when X and Y2, or X and Y1 represent a hydrogen atom at the same time, then Z represents a sulfur atom, and a process for preparing the same.
