91591-72-9 Usage
General Description
2,4-Dichloro-6-methylnicotinaldehyde is a chemical compound that belongs to the family of organic compounds known as pyridinecarboxaldehydes. It is a yellowish liquid with a strong odor, and it is primarily used in the manufacturing of agrochemicals and pharmaceuticals. 2,4-DICHLORO-6-METHYLNICOTINALDEHYDE is also known for its strong antimicrobial and pesticidal properties, making it an effective ingredient in various agricultural and industrial products. Additionally, it is used in the synthesis of other organic compounds and as a research tool in the field of chemical biology. The compound is also known for its moderate level of toxicity and should be handled with care.
Check Digit Verification of cas no
The CAS Registry Mumber 91591-72-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,5,9 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 91591-72:
(7*9)+(6*1)+(5*5)+(4*9)+(3*1)+(2*7)+(1*2)=149
149 % 10 = 9
So 91591-72-9 is a valid CAS Registry Number.
91591-72-9Relevant articles and documents
TOSYLACETATE BASED COMPOUNDS AND DERIVATIVES THEREOF AS PHGDH INHIBITORS
-
, (2018/10/19)
The present invention encompasses compounds of formula (I), wherein the groups R1 to R, A1 to A4 and n have the meanings given in the claims and specification, their use as inhibitors of PHGDH, pharmaceutical compositions
Potent, orally active corticotropin-releasing factor receptor-1 antagonists containing a tricyclic pyrrolopyridine or pyrazolopyridine core
Dyck, Brian,Grigoriadis, Dimitri E.,Gross, Raymond S.,Guo, Zhiqiang,Haddach, Mustapha,Marinkovic, Dragan,McCarthy, James R.,Moorjani, Manisha,Regan, Collin F.,Saunders, John,Schwaebe, Michael K.,Szabo, Tomas,Williams, John P.,Zhang, Xiaohu,Bozigian, Haig,Chen, Ta Rung
, p. 4100 - 4110 (2007/10/03)
Two new classes of tricyclic-based corticotropin-releasing factor (CRF 1) receptor-1 antagonists were designed by constraining known 1H-pyrrolo[2,3-b]pyridine and 1H-pyrazolo[3,4-b]pyridine ligands. Pyrrole- and pyrazole-based molecules 19g and
