98420-99-6 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
4-Bromo-2-propylpyridine is utilized as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals, contributing to the development of new drugs and pesticides due to its unique structural properties.
Used in Neurological Disorder Treatment:
In the medical field, 4-bromo-2-propylpyridine is studied for its potential therapeutic applications in treating neurological disorders such as Alzheimer's disease and Parkinson's disease, highlighting its role in improving patient care and quality of life.
Used as Insecticide and Fungicide:
4-Bromo-2-propylpyridine has been investigated for its insecticidal and fungicidal properties, making it a candidate for use in agricultural and environmental protection sectors to control pests and diseases, thereby enhancing crop yields and ecosystem health.
Check Digit Verification of cas no
The CAS Registry Mumber 98420-99-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,4,2 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 98420-99:
(7*9)+(6*8)+(5*4)+(4*2)+(3*0)+(2*9)+(1*9)=166
166 % 10 = 6
So 98420-99-6 is a valid CAS Registry Number.
98420-99-6Relevant academic research and scientific papers
INHIBITORS OF VIRAL REPLICATION, THEIR PROCESS OF PREPARATION AND THEIR THERAPEUTICAL USES
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Page/Page column 143, (2014/05/07)
Inhibitors of viral replication of formula (I), their process of preparation and their therapeutical uses. The present invention relates to compounds, their use in the treatment or the prevention of viral disorders, including HIV.
Modification of the pyridine moiety of non-peptidyl indole GnRH receptor antagonists.
Simeone, Joseph P,Bugianesi, Robert L,Ponpipom, Mitree M,Yang, Yi Tien,Lo, Jane-Ling,Yudkovitz, Joel B,Cui, Jisong,Mount, George R,Ren, Rena Ning,Creighton, Mellissa,Mao, An-Hua,Vincent, Stella H,Cheng, Kang,Goulet, Mark T
, p. 3329 - 3332 (2007/10/03)
The synthesis of a number of indole GnRH antagonists is described. Oxidation of the pyridine ring nitrogen, combined with alkylation at the two position, led to a compound with an excellent in vitro activity profile as well as oral bioavailability in both rats and dogs.
