69872-15-7 Usage
Description
3-Bromo-4-methyl-5-nitropyridine is a chemical compound characterized by the presence of a bromine atom at the 3rd position, a methyl group at the 4th position, and a nitro group at the 5th position on a pyridine ring. It is an organic synthetic intermediate with potential applications in various chemical and pharmaceutical processes.
Uses
Used in Pharmaceutical Industry:
3-Bromo-4-methyl-5-nitropyridine is used as a synthetic intermediate for the production of 4-bromo-6-azaindole and other azaindole derivatives. These azaindole compounds are of significant interest in the pharmaceutical industry due to their diverse biological activities and potential applications as therapeutic agents.
Used in Chemical Synthesis:
3-Bromo-4-methyl-5-nitropyridine serves as a key building block in the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, and other specialty chemicals. Its unique structural features allow for further functionalization and modification, enabling the development of new and innovative chemical entities with potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 69872-15-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,8,7 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 69872-15:
(7*6)+(6*9)+(5*8)+(4*7)+(3*2)+(2*1)+(1*5)=177
177 % 10 = 7
So 69872-15-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H5BrN2O2/c1-4-5(7)2-8-3-6(4)9(10)11/h2-3H,1H3
69872-15-7Relevant articles and documents
Prokopov,Yakhontov
, (1979)
SUBSTITUTED 5-CYANOINDOLE COMPOUNDS AND USES THEREOF
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Paragraph 00156, (2019/01/10)
A compound of Formula (I), or a pharmaceutically acceptable salt thereof, is provided that has been shown to be useful for the treatment of lysine (K)-specific demethylase 1A (LSD1) - mediated diseases or disorders, Formula (I), wherein R1, R2, R3, R4, and R5 are as defined herein.
Azaindolines: Derisking the indoline structural alert
Piatnitski Chekler, Eugene L.,Khan, Taukeer A.,Mamidala, Rajanikanth,Anderson, James T.,Tangirala, Raghuram S.,Verhoest, Patrick R.,Gilbert, Adam M.
, p. 377 - 379 (2012/01/31)
4-Substitued azaindolines, which are isosteres of indolines, are useful synthetic building blocks that reduce the risk of bioactivation induced idiosyncratic toxicity have been prepared. Multigram routes to 2,3-dihydro-1H-pyrrolo[2,3-c]pyridine-4-triflate 16, 2,3-dihydro-1H-pyrrolo[2,3- b]pyridine-4-carbonitrile 20 and 4-chloro-2,3-dihydro-1H-pyrrolo[2,3-d] pyridazine 30 are outlined.