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1,5-diphenyl-3-methoxycarbonal-1,2,4-triazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89060-64-0

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89060-64-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89060-64-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,0,6 and 0 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 89060-64:
(7*8)+(6*9)+(5*0)+(4*6)+(3*0)+(2*6)+(1*4)=150
150 % 10 = 0
So 89060-64-0 is a valid CAS Registry Number.

89060-64-0Relevant academic research and scientific papers

Transmission of substituent effects via 1,2,4-triazole ring residue

Shawali, Ahmad S.,Abbas, Ikhlass M.,Abdallah, Magda A.,Fahmi, Abdelgawad A.,Ahmad, Nada F.

, p. 1012 - 1016 (2007/10/02)

The ionization constants of a series of 5-phenyl-3-substituted phenyl-1,2,4-triazole-3-carboxylic acids (2a-j), prepared by the base catalysed rearrangement of 2-phenyl-4-arylazo-5-oxazolones (1a-j), and the rate of alkaline hydrolysis of the correspondin

An Improved Synthesis of 1H-1,2,4-Triazoles from C-Triphenylphosphinimino-hydrazones

Bruche, Luca,Garanti, Luisa,Zecchi, Gaetano

, p. 772 - 774 (2007/10/02)

1-Phenyl-1H-1,2,4-triazoles 5a-h are prepared in good yields by reaction of the triphenylphosphine imide 1 with acyl chlorides 2a-h and subsequent base treatment of the intermediate phosphonium salts 3a-h.

Ketone Enamines as Dipolarophiles towards C-Azidohydrazones

Bruche, Luca,Garanti, Luisa,Zecchi, Gaetano

, p. 1903 - 1906 (2007/10/02)

The reaction of methyl azido(phenylhydrazono)acetate (1) with the enamines (4)-(7) leads to different kinds of ring-closed products, namely 1,2,4-triazines (8)-(10), 1,2,3-triazoles (12)-(15), and 1,2,4-triazoles (16)-(19).An open-chain azo compound (20) is also formed.In one case, an intermediate 4,5-dihydro-1H-1,2,3-triazole (11) has been isolated.A mechanistic picture is proposed involving preliminary cycloaddition of the azido group to the enamine and subsequent reaction of the 4,5-dihydro-1H-1,2,3-triazoles according to various concurrent pathways.

Reaction of Hydrazonoyl Halides with N-Aryl Substituted Benzamidines

Anzani, Fulvio,Croce, Piero Dalla,Stradi, Riccardo

, p. 311 - 313 (2007/10/02)

The reaction between hydrazonoyl halides and N-arylbenzamidines leads to the simultaneous formation of products derived from a substitution and a cycloaddition reaction via two independent paths.

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