749875-02-3 Usage
Uses
Used in Pharmaceutical Industry:
3-Chloro-2-(trifluoroMethyl)isonicotinic acid is used as a key intermediate in the synthesis of various active pharmaceutical ingredients. Its unique structure and properties make it a valuable component in the development of new drugs.
Used in Agrochemicals:
TFMI acid is utilized in the synthesis of agrochemicals, contributing to the development of effective and innovative products for agricultural applications.
Used in Organic Chemistry:
3-Chloro-2-(trifluoroMethyl)isonicotinic acid is used as a building block for the preparation of potential anti-tuberculosis agents, showcasing its potential in the synthesis of compounds with significant therapeutic applications.
Used in Research and Development:
TFMI acid is employed in research and development for its unique structural and chemical properties, which allow for the exploration of new applications and the advancement of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 749875-02-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,9,8,7 and 5 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 749875-02:
(8*7)+(7*4)+(6*9)+(5*8)+(4*7)+(3*5)+(2*0)+(1*2)=223
223 % 10 = 3
So 749875-02-3 is a valid CAS Registry Number.
749875-02-3Relevant articles and documents
GLYCINE TRANSPORTER INHIBITOR
-
Page/Page column 109, (2010/11/30)
The present invention provides a compound represented by the following formula or a pharmaceutically acceptable salt of the compound or a hydrate of the compound or the salt, which is useful for the prevention or treatment of diseases such as schizophreni
Further metalations and functionalizations of chloro-, bromo- and iodo(trifluoromethyl)pyridines
Cottet, Fabrice,Marull, Marc,Mongin, Florence,Espinosa, David,Schlosser, Manfred
, p. 1619 - 1624 (2007/10/03)
In accordance with the concept of regioexhaustive functionalization, both 3-chloro-2-(trifluoromethyl)pyridine and 2-bromo-6-(trifluoromethyl)pyridine were converted each time into the three possible carboxylic acids (1, 4 and 5 and 6, 9 and 12, respectively). 2-Bromo-4-(trifluoromethyl)pyridine, 2-bromo-5-(trifluoromethyl)pyridine, 2-iodo-4-(trifluoromethyl)pyridine and 4-iodo-2-(trifluoromethyl)pyridine were selectively deprotonated and subsequently carboxylated at the respective 3-positions thus affording the acids 13-16. Finally, the N-pivaloyl-protected 2-amino-3-chloro-5-(trifluoromethyl) pyridine was deprotonated at the 4-position and the intermediate trapped with iodine and benzaldehyde to provide, after amide cleavage, the aminopyridines 17 and 18.