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1H-Pyrrole-2-carboxaldehyde, phenylhydrazone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81280-72-0

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81280-72-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81280-72-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,2,8 and 0 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 81280-72:
(7*8)+(6*1)+(5*2)+(4*8)+(3*0)+(2*7)+(1*2)=120
120 % 10 = 0
So 81280-72-0 is a valid CAS Registry Number.

81280-72-0Downstream Products

81280-72-0Relevant academic research and scientific papers

Determination of the apparent molar refraction and partial molar volume at infinite dilution of thiophene-, pyrrole- and furan-2-carboxaldehyde phenylhydrazone derivatives in acetonitrile at 293.15 K

Alvarado, Ysaias J.,Caldera-Luzardo, Jose,Ferrer-Amado, Gladys,Mancilla-Labarca, Victoria,Michelena, Elba

, p. 1 - 11 (2007)

High-precision densitometry and high-accuracy refractometry measurements of extremely dilute solutions of the thiophene-2- (TCPH), pyrrole-2- (PCPH) and furan-2-carboxaldehyde-phenylhydrazone (FCPH) compounds in acetonitrile have been obtained at 293.15 K

A class of highly effective broad-spectrum plant antimicrobial agentS

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Paragraph 0036; 0043-0045; 0072, (2022/03/27)

The present invention relates to a class of benzohydrazone compounds and synthetic methods thereof and drugs containing the compound thereof and applications thereof. The hydrate compounds involved in the present invention have the advantages of simple structure, easy synthesis, strong antibacterial activity, wide antibacterial spectrum, small toxicity to animals and plants and low composition, and can be used as active ingredients or synergistic ingredients for the development of new high-efficiency broad-spectrum plant antibacterial agents.

Open vessel and cooling while heating microwave-assisted synthesis of pyridinyl N-Aryl hydrazones

La Regina, Giuseppe,Gatti, Valerio,Piscitelli, Francesco,Silvestri, Romano

experimental part, p. 2 - 6 (2011/04/15)

We reported the first example of open vessel and cooling while heating microwave-assisted synthesis of pyridinyl N-aryl hydrazones. Compounds were prepared in excellent isolated yields (88-98%) in only 5 min, by reacting 4- and 2,4-(di)substituted phenylhydrazines, bearing both electron-donating (4-CH 3, 4-OCH3) and -withdrawing (4-Cl, 4-Br, 4-CF3, 4-NO2, 2,4-Cl2) groups with 2-, 3-, and 4-acetylpyridine. The method was successfully extended to other carbonyl compounds.

Solubility of thiophene-, furan- and pyrrole-2-carboxaldehyde phenylhydrazone derivatives in 2.82 mol?L-1 aqueous DMSO at 298.15 K, inhibition of lymphoproliferation and tubulin polymerization: A study based on the scaled particle theory

Alvarado, Ysaías J.,álvarez-Mon, Melchor,Baricelli, Joanna,Caldera-Luzardo, José,Cubillán, Néstor,Ferrer-Amado, Gladys,Hassanhi, Manzur,Marrero-Ponce, Yovani,Mancilla, Victoria,Rocafull, Miguel A.,San?Antonio-Sánchez, Mari?a Esther,Ojeda-Andara, José,Thomas, Luz E.

body text, p. 1099 - 1112 (2011/05/30)

In this work, the solubilities of nine phenylhydrazone derivatives in water and in 2.82 mol ? L-1 aqueous DMSO at 298.15 K, expressed on the molar fraction scale, are reported. The estimated value of the standard Gibbs energy for transferring t

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