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[3-(4-methylphenyl)-1-phenyl-1H-pyrazol-5-yl]acetonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

153391-34-5

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153391-34-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 153391-34-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,3,9 and 1 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 153391-34:
(8*1)+(7*5)+(6*3)+(5*3)+(4*9)+(3*1)+(2*3)+(1*4)=125
125 % 10 = 5
So 153391-34-5 is a valid CAS Registry Number.

153391-34-5Downstream Products

153391-34-5Relevant academic research and scientific papers

5-Cyanomethyl-3-(4-methylphenyl)-1-phenylpyrazole

Singh, Sanjay K.,Kumar, Ajay,Vats, Archana,Bisht, Kirpal S.,Parmar, Virinder S.,Errington, William

, p. 2404 - 2406 (1995)

The title nitrile, 3-(4-methylphenyl)-1-phenylpyrazole-5-acetonitrile, C18H15N3, is one of the products obtained from the reaction of 3-cyano-6-(4-methylphenyl)-4-methylthio-2-oxo-2H-pyran with phenylhydrazine.The asymmetric unit contains two almost identical molecules differing only in the orientations of the phenyl and methylphenyl groups with respect to the planar pyrazole nucleus.

Synthesis of E- and Z-Pyrazolylacrylonitriles and their evaluation as novel antioxidants

Parmar, Virinder S.,Kumar, Ajay,Prasad, Ashok K.,Singh, Sanjay K.,Kumar, Naresh,Mukherjee, Shubhasish,Raj, Hanumantharao G.,Goel, Sanjay,Errington, William,Puar, Mohindar S.

, p. 1425 - 1436 (2007/10/03)

A facile synthesis of (Z)- and (E)-2-(5-arylpyrazol-3-yl)-3-(pyrrol-2-yl)acrylonitriles and (Z)-2-(1,3-diarylpyrazol-5-yl)-3-(pyrrol-2-yl)acrylonitriles, and isomerisation of (Z)-2-(5-arylpyrazolyl)acrylonitriles to (E)-2-(5-arylpyrazolyl)acrylonitriles under basic conditions have been reported. (Z)-2-(1,3-Diarylpyrazolyl)acrylonitriles did not undergo isomerisation under the similar conditions. New compounds were identified on the basis of their spectral data (1H-, 13C-, 1H-1H COSY, NOESY, NOE, HMQC NMR, IR, UV and EI mass). The structures of one acrylonitrile and five of their precursor 6-arylpyran-2-ones and cyanomethylpyrazoles were confirmed by X-ray crystallographic studies. Effects of pyrazolylacrylonitriles and their precursors on rat liver-microsomal lipid peroxidation were evaluated in vitro with a view to establish structure-activity relationship and to identify a lead compound. Copyright (C) 1999 Elsevier Science Ltd.

Ring transformation reaction: Part II - Reaction specificity of hydrazines towards 6-aryl-4-(methylthio)-2-oxo-2H-pyran-3-carbonitriles and corresponding 3-ethyl carboxylate

Ram, Vishnu Ji,Haque, Navedul,Singh, Sanjay Kumar,Hussaini, Falak Anwer,Shoeb, Aboo

, p. 924 - 928 (2007/10/02)

Reaction specificity of hydrazine hydrate, cyclohexyl- and phenyl-hydrazines towards 6- or 5,6-disubstituted-4-(methylthio)-2-oxo-2H-pyran-3-carbonitriles and the corresponding 3-ethyl carboxylate (1,8) has been studied.

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