351457-86-8 Usage
General Description
5-BROMO-3-FORMYL-4-METHYLPYRIDINE is a chemical compound with the molecular formula C7H6BrNO. It is a derivative of pyridine, containing a bromine atom at position 5 and a formyl group at position 3, along with a methyl group at position 4. 5-BROMO-3-FORMYL-4-METHYLPYRIDINE is widely used in organic synthesis as a building block for various pharmaceuticals, agrochemicals, and other fine chemicals. It is known for its ability to undergo various chemical reactions, such as nucleophilic substitution and condensation, making it a versatile intermediate in the production of complex organic molecules. Additionally, it has potential applications in the field of medicinal chemistry, particularly in the development of new drugs and drug delivery systems. Overall, 5-BROMO-3-FORMYL-4-METHYLPYRIDINE plays a crucial role in the synthesis of diverse compounds with biological and pharmaceutical significance.
Check Digit Verification of cas no
The CAS Registry Mumber 351457-86-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,1,4,5 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 351457-86:
(8*3)+(7*5)+(6*1)+(5*4)+(4*5)+(3*7)+(2*8)+(1*6)=148
148 % 10 = 8
So 351457-86-8 is a valid CAS Registry Number.
351457-86-8Relevant articles and documents
INDAZOLES AS WNT/B-CATENIN SIGNALING PATHWAY INHIBITORS AND THERAPEUTIC USES THEREOF
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, (2011/02/26)
Described herein are methods of treating a disorder or disease in which aberrant Wnt signaling is implicated, with a variety of compounds, including Wnt inhibitor compounds. More particularly, it concerns the use of an indazole compound or analogs thereof
Synthesis and evaluation of pyrazolo[3,4-b]pyridine CDK1 inhibitors as anti-tumor agents
Lin, Ronghui,Connolly, Peter J.,Lu, Yanhua,Chiu, George,Li, Shengjian,Yu, Yang,Huang, Shenlin,Li, Xun,Emanuel, Stuart L.,Middleton, Steven A.,Gruninger, Robert H.,Adams, Mary,Fuentes-Pesquera, Angel R.,Greenberger, Lee M.
, p. 4297 - 4302 (2008/02/11)
A series of 3,5-disubstituted pyrazolo[3,4-b]pyridine cyclin-dependent kinase (CDK) inhibitors was synthesized. These compounds showed potent and selective CDK inhibitory activities and inhibited in vitro cellular proliferation in cultured human tumor cel
SYNTHESIS OF 5-BROMO-4-METHYL-PYRIDIN-3-YLMETHYL)-ETHYL-CARBAMIC ACID TERT-BUTYL ESTER
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Page/Page column 8, (2010/11/08)
The present invention relates to novel synthetic methods for the preparation of intermediates of 3{5-[3-(4,6-Difluoro-1H-benzoimidazol-2-yl)-1H-indazol-5-yl]-4-methyl-pyridin-3-ylmethyl}-ethyl-amine.