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ethyl 5-methyl-1-phenyl-3-(thiophen-2-yl)-1H-pyrazole-4-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

116709-43-4

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116709-43-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 116709-43-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,7,0 and 9 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 116709-43:
(8*1)+(7*1)+(6*6)+(5*7)+(4*0)+(3*9)+(2*4)+(1*3)=124
124 % 10 = 4
So 116709-43-4 is a valid CAS Registry Number.

116709-43-4Downstream Products

116709-43-4Relevant academic research and scientific papers

Sc(OTf)3-catalyzed, solvent-free domino synthesis of functionalized pyrazoles under controlled microwave irradiation

Kumari, Kumkum,Raghuvanshi, Dushyant Singh,Jouikov, Viatcheslav,Singh, Krishna Nand

experimental part, p. 1130 - 1133 (2012/03/26)

An efficient, rapid, and green synthesis of functionalized pyrazoles has been accomplished under solvent-free conditions by the reaction of phenyl hydrazine, aldehydes and ethyl acetoacetate. This approach exploits the synthetic potential of microwave irr

Regioselective multicomponent synthesis of fully substituted pyrazoles and bispyrazoles catalyzed by zinc triflate

Safaei, Shirin,Mohammadpoor-Baltork, Iraj,Khosropour, Ahmad Reza,Moghadam, Majid,Tangestaninejad, Shahram,Mirkhani, Valiollah

experimental part, p. 2214 - 2222 (2011/10/18)

A variety of fully substituted pyrazoles were easily prepared through a three-component condensation of aldehydes, arylhydrazines, and ethyl acetoacetate in the presence of catalytic amounts of zinc triflate [Zn(OTf) under solvent-free conditions. Selecti

Chemistry of C-Heteroarylnitrilimines. Synthesis and Cycloaddition Reactions of N-Phenyl-C-(2-thienyl)nitrilimine

Hassaneen, Hamdi M.,Mousa, Hiyam A. H.,Shawali, Ahmad S.

, p. 1665 - 1668 (2007/10/02)

The nitrilimine 7, generated in situ from N-phenyl-C-(2-thienyl)formohydrazidoyl chloride 5 in chloroform in the presence of triethylamine, reacts with acrylonitrile, acrylamide and arylidene acetophenones to give exclusively the 5-substituted 2-pyrazolin

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