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(E)-3-phenyl-2-(3-thienyl)acrylonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13781-54-9

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13781-54-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13781-54-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,7,8 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 13781-54:
(7*1)+(6*3)+(5*7)+(4*8)+(3*1)+(2*5)+(1*4)=109
109 % 10 = 9
So 13781-54-9 is a valid CAS Registry Number.

13781-54-9Relevant academic research and scientific papers

Three substituted (E)-3-aryl-2-(thienyl)-acrylonitriles: Isolated molecules, simple hydrogen-bonded chains and hydrogen-bonded sheets

Cobo, Debora,Quiroga, Jairo,De La Torre, Jose M.,Cobo, Justo,Low, John N.,Glidewell, Christopher

, p. o550-o553 (2006)

The structure of (E)-2-(2-thienyl)-3-(3,4,5-trimethoxyphenyl)- acrylonitrile, C16H15NO3S, contains no direction-specific intermolecular interactions. The molecules of (E)-3-(4-bromophenyl)-2-(2-thienyl)acrylonitrile, Csub

Synthesis and evaluation of novel E-2-(2-thienyl)- and Z-2-(3-thienyl)-3- arylacrylonitriles as antifungal and anticancer agents

Quiroga, Jairo,Cobo, Debora,Insuasty, Braulio,Abonia, Rodrigo,Nogueras, Manuel,Cobo, Justo,Vasquez, Yelkaira,Gupta, Mahabir,Derita, Marcos,Zacchino, Susana

, p. 603 - 606 (2008/12/21)

A series of 3-aryl-2-(2-thienyl)acrylonitriles 7 and 3-aryl-2-(3-thienyl) acrylonitriles 8 were synthesized by the reaction of aromatic aldehydes 6 with 2- and 3-thienylacetonitriles 4 and 5, and evaluated for antifungal and cytotoxic activities against a

Benzannelated Analogs of Phenanthro- and thiophene: Synthesis and Structural Characterization by Two-Dimensional NMR and X-Ray Techniques

Stuart, John G.,Quast, Michael J.,Martin, Gary E.,Lynch, Vincent M.,Simonsen, Stanley H.,et al.

, p. 1215 - 1234 (2007/10/02)

Syntheses of benzophenanthrothiophene, benzophenanthrothiophene and their 1-methyl analogs are reported as potential constituents of solvent refined coal liquids and for mutagenicity testing.The attempted synthesis of the 13-methyl

Kinetic Study of the Base-catalysed Reactions of Benzaldahehyde and Thiophene-2-carbaldehyde with Acetonitriles

Alberghina, Gaetano,Amato, Maria Emanuela,Corsaro, Antonio,Fisichella, Salvatore,Scarlata, Giuseppe

, p. 353 - 356 (2007/10/02)

The reaction rates of the sodium methoxide-catalysed condensation of benzaldehyde and thiophene-2-carbaldehyde with heteroaromatic acetonitriles ArCH2CN; Ar = C6H5, C6H4CH3(p), C6H4-OCH3(p), C6H4F(p), C6H4Cl(p), C6H4Br(p), 2-thienyl, 3-thienyl, 3-pyridyl

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