745833-19-6 Usage
Uses
Used in Pharmaceutical Industry:
Ethyl 2-(2,4-difluorophenyl)-6-chloronicotinate is used as an intermediate in the synthesis of various pharmaceutical drugs. Its unique chemical structure and properties contribute to the development of new and effective medications.
Used in Drug Discovery and Development:
Ethyl 2-(2,4-difluorophenyl)-6-chloronicotinate is used as a key component in drug discovery and development due to its potential therapeutic applications and significant biological activities. It aids in the identification and optimization of new drug candidates.
Used in Chemical Research:
Ethyl 2-(2,4-difluorophenyl)-6-chloronicotinate is used in chemical research for its unique chemical and physical properties. It serves as a versatile compound for exploring various research applications and advancing the understanding of fluoro substituted pyridine derivatives.
Check Digit Verification of cas no
The CAS Registry Mumber 745833-19-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,5,8,3 and 3 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 745833-19:
(8*7)+(7*4)+(6*5)+(5*8)+(4*3)+(3*3)+(2*1)+(1*9)=186
186 % 10 = 6
So 745833-19-6 is a valid CAS Registry Number.
InChI:InChI=1/C14H10ClF2NO2/c1-2-20-14(19)10-5-6-12(15)18-13(10)9-4-3-8(16)7-11(9)17/h3-7H,2H2,1H3
745833-19-6Relevant articles and documents
SOLID FORMS OF 2-(2, 4-DIFLUOROPHENYL)-6-(1-(2,6-DIFLUOROPHENYL)UREIDO)NICOTINAMIDE
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Page/Page column 46, (2010/09/03)
This invention relates to solid forms of 2-(2, 4-difluorophenyl)-6-(l- (2,6-difluorophenyl)ureido)nicotinamide and pharmaceutical compositions thereof, and methods and uses therewith.
PROCESSES FOR PRODUCING PHENYL-6-(1-(PHENYL)UREIDO)NICOTINAMIDES)
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Page/Page column 23-24, (2010/09/03)
The present invention relates to processes for the preparation of compounds useful as inhibitors of p38 kinase. The processes of the present invention are amenable for large scale preparation and produce stable phenyl-6-(l-(phenyl)ureido)nicotinamides in