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1,3-diphenyl-1H-thieno[3,2-c]pyrazole is a chemical compound with the molecular formula C17H12N2S. It is a heterocyclic compound, specifically a pyrazole fused with a thiophene ring. 1,3-diphenyl-1H-thieno[3,2-c]pyrazole is characterized by two phenyl groups attached to the 1 and 3 positions of the pyrazole ring, and a sulfur atom in the thiophene ring. It is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and properties. The compound is typically synthesized through various chemical reactions and can be used as a building block for more complex molecules. Its stability, reactivity, and potential applications make it an interesting subject for research in the field of organic chemistry.

7716-41-8

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7716-41-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7716-41-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,1 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7716-41:
(6*7)+(5*7)+(4*1)+(3*6)+(2*4)+(1*1)=108
108 % 10 = 8
So 7716-41-8 is a valid CAS Registry Number.

7716-41-8Downstream Products

7716-41-8Relevant academic research and scientific papers

An efficient transition-metal-free synthesis of 1H-indazoles from arylhydrazones with montmorillonite K-10 under O2 atmosphere

Yu, Jin,Lim, Jin Woo,Kim, Su Yeon,Kim, Jimin,Kim, Jae Nyoung

, p. 1432 - 1436 (2015)

An efficient transition-metal-free synthetic method of 1H-indazoles has been developed. The reaction of arylhydrazones in the presence of montmorillonite K-10 in 1,2-dichlorobenzene at 130 °C afforded 1H-indazoles in good yields most likely via a sequenti

[Bis-(trifluoroacetoxy)iodo]benzene-Mediated Oxidative Direct Amination C–N Bond Formation: Synthesis of 1H-Indazoles

Zhang, Zhiguo,Huang, Yuanyuan,Huang, Guoqing,Zhang, Guisheng,Liu, Qingfeng

, p. 2426 - 2433 (2017/07/24)

An efficient [bis-(trifluoroacetoxy)iodo]benzene (PIFA)-mediated oxidative C-N bond formation is developed for the synthesis of 1H-indazoles from readily available arylhydrazones. The reaction tolerates a wide range of functional groups and has broad scope of substrates. Moreover, this method is a relative green and reliable method for rapid preparation of substituted 1H-indazoles under mild conditions.

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