38841-52-0 Usage
Uses
Used in Pharmaceutical Industry:
2,6-diamino-3-cyano-4-methylpyridine is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique chemical structure allows it to be incorporated into the development of new drugs, contributing to the advancement of medicine.
Used in Agrochemical Industry:
In the agrochemical sector, 2,6-diamino-3-cyano-4-methylpyridine serves as an essential intermediate for the production of agrochemicals. Its properties make it suitable for the creation of compounds that can be used in agriculture to protect crops and enhance yields.
Used in Research and Development:
2,6-diamino-3-cyano-4-methylpyridine is utilized in research and development for its potential applications in creating new chemical entities. Its versatility in chemical reactions makes it a valuable tool for scientists exploring novel compounds and their potential uses in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 38841-52-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,8,4 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 38841-52:
(7*3)+(6*8)+(5*8)+(4*4)+(3*1)+(2*5)+(1*2)=140
140 % 10 = 0
So 38841-52-0 is a valid CAS Registry Number.
38841-52-0Relevant academic research and scientific papers
NEW TRPA1 ANTAGONISTS
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Page/Page column 126; 127, (2017/08/01)
The present invention relates to compounds of Formula (I), to the process for preparing such compounds and to their use in the treatment of a pathological condition or disease susceptible to amelioration by TRPA1 channel inhibition or antagonism.
Synthesis and Reactivity of 2,6-Diamino-4-methyl-3-pyridinecarbonitrile
Katritzky, Alan R.,Rachwal, Stanislaw,Smith, Terrance P.,Steel, Peter J.
, p. 979 - 984 (2007/10/02)
2,6-Dihydroxy-4-methyl-3-pyridinecarbonitrile is converted via its 2,6-dichloro analog into the corresponding 2-amino-6-chloro, 2-chloro-6-amino, and 2,6-diamino derivatives.The last reacts with benzenesulfonyl chloride to yield a tris-sulfonyl derivative, the structure of which is demonstrated by X-ray analysis.
