1503-68-0 Usage
Description
1-(5-chloro-6-oxo-1-phenyl-1,6-dihydropyridazin-4-yl)triaza-1,2-dien-2-ium is a chemical compound that belongs to the dihydropyridazine class. It features a triaza-dien-ium group and a chloro-oxo-phenyl substituent, which may contribute to its potential pharmacological activities and suitability as a drug candidate.
Uses
Used in Pharmaceutical Development:
1-(5-chloro-6-oxo-1-phenyl-1,6-dihydropyridazin-4-yl)triaza-1,2-dien-2-ium is used as a potential drug candidate for [application reason] due to its dihydropyridazine structure and the presence of the chloro and phenyl groups, which may enhance its biological activities.
Further research and investigation are required to fully understand the properties and potential applications of this chemical compound in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 1503-68-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,0 and 3 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1503-68:
(6*1)+(5*5)+(4*0)+(3*3)+(2*6)+(1*8)=60
60 % 10 = 0
So 1503-68-0 is a valid CAS Registry Number.
1503-68-0Relevant articles and documents
Targeting the Warburg Effect in cancer; Relationships for 2-arylpyridazinones as inhibitors of the key glycolytic enzyme 6-phosphofructo-2-kinase/2,6-bisphosphatase 3 (PFKFB3)
Brooke, Darby G.,Van Dam, Ellen M.,Watts, Colin K.W.,Khoury, Amanda,Dziadek, Marie A.,Brooks, Hilary,Graham, Lisa-Jane K.,Flanagan, Jack U.,Denny, William A.
, p. 1029 - 1039 (2014/02/14)
High-throughput screening of a small-molecule library identified a 5-triazolo-2-arylpyridazinone as a novel inhibitor of the important glycolytic enzyme 6-phosphofructo-2-kinase/2,6-bisphosphatase 3 (PFKFB3) Such inhibitors are of interest due to PFKFB3's
A "click and activate" Approach in one-pot synthesis of a triazolyl-pyridazinone library
Qian, Wenyuan,Winternheimer, David,Allen, Jennifer
supporting information; experimental part, p. 1682 - 1685 (2011/05/03)
A "click and activate" strategy was designed and executed in a four-component, stepwise condensation that led to a trisubstituted triazolyl-pyridazinone library. This one-pot process included regioselective azide substitution at 2-substituted-4,5-dichloro