90734-72-8 Usage
Uses
Used in Medicinal Chemistry:
(6-CHLOROIMIDAZO[1,2-B]PYRIDAZIN-3-YL)(PHENYL)METHANONE is used as a building block for the synthesis of pharmaceuticals due to its unique molecular structure and potential to interact with biological targets, contributing to the development of new therapeutic agents.
Used in Biologically Active Compounds Synthesis:
In the field of biologically active compounds, (6-CHLOROIMIDAZO[1,2-B]PYRIDAZIN-3-YL)(PHENYL)METHANONE serves as an intermediate, leveraging its structural components to create molecules with specific biological activities, which may be beneficial in various therapeutic areas.
Used in Targeted Drug Design:
(6-CHLOROIMIDAZO[1,2-B]PYRIDAZIN-3-YL)(PHENYL)METHANONE is used as a component in targeted drug design, where its chloro and phenyl groups may facilitate specific interactions with molecular targets, enhancing the compound's efficacy and selectivity in treating diseases.
Used in Chemical Synthesis and Modification:
The methanone functional group in (6-CHLOROIMIDAZO[1,2-B]PYRIDAZIN-3-YL)(PHENYL)METHANONE allows it to be used in chemical synthesis and modification processes, where its reactivity can be exploited to create new compounds or modify existing ones for improved performance or novel applications.
Check Digit Verification of cas no
The CAS Registry Mumber 90734-72-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,7,3 and 4 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 90734-72:
(7*9)+(6*0)+(5*7)+(4*3)+(3*4)+(2*7)+(1*2)=138
138 % 10 = 8
So 90734-72-8 is a valid CAS Registry Number.
90734-72-8Relevant articles and documents
Convenient two-step one-pot synthesis of 3-substituted imidazo[1,2-a]pyridines and imidazo[1,2-b]pyridazines
Fan, Hongli,Li, Fenghai
, (2018/05/23)
Abstract: A convenient and novel two-step one-pot method for the synthesis of 3-substituted imidazo[1,2-a]pyridines and 3-substituted imidazo[1,2-b]pyridazines was developed through the reaction of heterocyclic amines and N,?N-dimethylformamide dimethyl a
Imidazopyridazines. XVI. Synthesis and Central Nervous System Activities of Some 6-(Chloro, Alkylthio, Phenylthio, Benzylthio or Pyridinylmethylthio)-3-(unsubstituted, benzamidomethyl or methoxy)-2-(styryl or benzoyl)imidazopyridazines
Barlin, Gordon B.,Davies, Les P.,Harrison, Peter W.,Jacobsen, Noel W.,Willis, Anthony C.
, p. 1989 - 2000 (2007/10/02)
Some 6-(chloro, alkylthio, phenylthio, benzylthio or pyridinylmethylthio)-3-(unsubstituted, benzamidomethyl or methoxy)-2-styrylimidazopyridazines and 6-chloro-3-(unsubstituted and benzamidomethyl)-2-benzoylamidazopyridazines have been prepa
