6956-41-8 Usage
Description
(6Z)-6-(1,5-diphenylpyrazolidin-3-ylidene)cyclohexa-2,4-dien-1-one is a synthetic organic compound belonging to the pyrazolidin-3-ylidene class, featuring a complex molecular structure with a cyclohexa-2,4-dien-1-one moiety. (6Z)-6-(1,5-diphenylpyrazolidin-3-ylidene)cyclohexa-2,4-dien-1-one holds promise in medicinal chemistry and drug development due to its diverse biological activities, such as anti-inflammatory and analgesic properties. Its unique structural features make it an intriguing candidate for further research and potential drug design, although its precise biological and pharmacological properties and mechanisms of action are still under investigation.
Uses
Used in Pharmaceutical Industry:
(6Z)-6-(1,5-diphenylpyrazolidin-3-ylidene)cyclohexa-2,4-dien-1-one is used as a potential therapeutic agent for its anti-inflammatory and analgesic properties, which can be beneficial in the development of new medications to treat various conditions associated with pain and inflammation.
Used in Medicinal Chemistry Research:
(6Z)-6-(1,5-diphenylpyrazolidin-3-ylidene)cyclohexa-2,4-dien-1-one serves as a subject of interest in medicinal chemistry research, where its structural features and biological activities are being studied to understand its potential applications in drug design and the development of novel therapeutics.
Used in Drug Development:
(6Z)-6-(1,5-diphenylpyrazolidin-3-ylidene)cyclohexa-2,4-dien-1-one is utilized in drug development as a starting point or a lead compound for the creation of new drugs, particularly those targeting inflammation and pain management. Its unique structure and biological activities make it a valuable candidate for further optimization and development into effective pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 6956-41-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,5 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6956-41:
(6*6)+(5*9)+(4*5)+(3*6)+(2*4)+(1*1)=128
128 % 10 = 8
So 6956-41-8 is a valid CAS Registry Number.
6956-41-8Relevant articles and documents
Microwave enhanced green synthesis of 2-pyrazolines, isoxazolines and cyclohexenones
Al-Bogami, Abdullah S.,Alkhathlan, Hamad Z.,Saleh, Tamer S.
, p. 6427 - 6433 (2013)
Hydroxy chalcones undergo simple cyclizations with phenylhydrazine to afford 2-pyrazolines under microwave irradiation in the presence of glacial AcOH as cyclizing agent, also undergo simple cyclizations with hydroxylamine to afford 2-isoxazolines under m
TfOH mediated intermolecular electrocyclization for the synthesis of pyrazolines and its application in alkaloid synthesis
Annes, Sesuraj Babiola,Vairaprakash, Pothiappan,Ramesh, Subburethinam
, p. 30071 - 30075 (2018/09/11)
TfOH mediated easy access to interesting pyrazolines starting from an aldehyde, phenylhydrazine and styrene has been developed. The scope of this synthetic methodology has been explored by synthesizing various 1,3,5-trisubstituted pyrazolines in very good yields with very high regioselectivity. The origin of regioselectivity has been explained by comparing the stability of possible intermediate carbocations. The synthetic utility of a green solvent has been explored by synthesizing some of pyrazolines in a DES medium. The synthetic application of the present methodology is employed in the synthesis of a pyrazoline alkaloid.
A novel methodology for synthesis of dihydropyrazole derivatives as potential anticancer agents
Wang, Xu,Pan, Ying-Ming,Huang, Xiao-Chao,Mao, Zhong-Yuan,Wang, Heng-Shan
supporting information, p. 2028 - 2032 (2014/03/21)
A novel, simple, and efficient method for the synthesis of 4,5-dihydropyrazole derivatives has been developed. The reaction proceeded through the base-induced isomerization of easily accessible propargyl alcohols followed by cyclization of α,β-unsaturated hydrazones. Furthermore, selected compounds 3ab and 3ac exhibited good activities against Bel-7404 (human hepatoma cancer), HepG2 (human liver cancer), NCI-H460 (human lung cancer) and SKOV3 (human ovarian cancer) cell lines with IC50 in the range of 22-46 μmol L-1.
