929613-64-9 Usage
1-chloro-4-(phenylthioMethyl)phthalazine
A chemical compound consisting of 14 carbon atoms, 9 hydrogen atoms, 1 chlorine atom, 2 nitrogen atoms, and 1 sulfur atom.
Phthalazine derivative
A compound based on the phthalazine structure, which is a fused system of two benzene rings and a diazine ring (two nitrogen atoms).
Chlorine atom
A halogen element present in the compound, which may influence its reactivity and biological activity.
Phenylthiomethyl group
A functional group consisting of a benzene ring attached to a methylene group (-CH2-) and a sulfur atom (-S-), which may also affect the compound's reactivity and biological activity.
Potential applications in medicinal chemistry
The compound may have pharmacological properties that could be useful in the development of new drugs or therapies.
Influence of chlorine and phenylthiomethyl group on reactivity and biological activity
The presence of these groups may alter the compound's chemical and biological properties, making it a subject of interest for further research.
Need for further studies
Additional research is necessary to explore the potential uses and effects of 1-chloro-4-(phenylthioMethyl)phthalazine in medicinal and pharmaceutical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 929613-64-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,9,6,1 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 929613-64:
(8*9)+(7*2)+(6*9)+(5*6)+(4*1)+(3*3)+(2*6)+(1*4)=199
199 % 10 = 9
So 929613-64-9 is a valid CAS Registry Number.
929613-64-9Relevant articles and documents
Synthesis and anticancer activities of novel 1,4-disubstituted phthalazines
Li, Juan,Zhao, Yan-Fang,Yuan, Xiao-Ye,Xu, Jing-Xiong,Gong, Ping
, p. 574 - 582 (2007/10/03)
A series of novel 1-anilino-4-(arylsulfanylmethyl)phthalazines were designed and synthesized. The structures of all the compounds were confirmed by IR, 1H-NMR, elemental analysis and MS. The analogues 1-(3-chloro-4-fluoroanilino)-4-(3,4-difluorophenylthio-methyl)phthalazine (12) and 1-(4-fluoro-3-trifluoromethylanilino)-4-(3,4-difluorophenyl-thiomethyl) phthalazine (13) showed higher activity than a cisplatin control when tested in vitro against two different cancer cell lines using the microculture tetrazolium method (MTT) method.
