959163-01-0 Usage
General Description
6-chloro-4-(ethylamino)-3-Pyridinecarboxaldehyde is a chemical compound with the molecular formula C8H9ClN2O. It is a yellow to brown powder that is commonly used in pharmaceutical research and development as an intermediate in the synthesis of various pharmaceuticals. 6-chloro-4-(ethylamino)-3-Pyridinecarboxaldehyde is also utilized as a building block in the production of agrochemicals, dyes, and other fine chemicals. It has potential applications in the pharmaceutical industry due to its ability to act as a precursor for the synthesis of various drugs and pharmaceutical compounds. Additionally, it is important to handle this chemical with care, as it may pose certain health and environmental risks if not properly managed.
Check Digit Verification of cas no
The CAS Registry Mumber 959163-01-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,9,1,6 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 959163-01:
(8*9)+(7*5)+(6*9)+(5*1)+(4*6)+(3*3)+(2*0)+(1*1)=200
200 % 10 = 0
So 959163-01-0 is a valid CAS Registry Number.
959163-01-0Relevant articles and documents
GEM-DISUBSTITUTED HETEROCYCLIC COMPOUNDS AND THEIR USE AS IDH INHIBITORS
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Page/Page column 39-40, (2021/05/15)
The present invention relates to certain gem-disubstituted heterocyclic compounds, which modulate the activity of Isocitrate Dehydrogenase (IDH). The compounds of this invention are therefore useful in treating diseases caused by mutated IDH1 and/or mutat
HETEROCONDENSED PYRIDONES COMPOUNDS AND THEIR USE AS IDH INHIBITORS
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Page/Page column 53; 55, (2019/12/15)
The present invention relates to certain substituted heterocondensed pyridone analogues of formula (I) which modulate the activity of Isocitrate Dehydrogenase (IDH). The compounds of this invention are therefore useful in treating diseases caused by mutat
INHIBITORS OF THE FIBROBLAST GROWTH FACTOR RECEPTOR
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Paragraph 0153; 0158; 0159, (2015/07/22)
Described herein are inhibitors of FGFR-4, pharmaceutical compositions including such compounds, and methods of using such compounds and compositions to inhibit the activity of FGFR-4.