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Benzaldehyde-(2-fluoro-phenylhydrazone) is a chemical compound derived from the condensation of benzaldehyde with 2-fluorophenylhydrazine. This organic molecule features a benzene ring with a formyl group (CHO) attached to one carbon and a 2-fluorophenylhydrazone moiety on the adjacent carbon. The 2-fluorophenylhydrazone group consists of a 2-fluorophenyl ring connected to a hydrazine molecule through an azomethine linkage (-N=N-). benzaldehyde-(2-fluoro-phenylhydrazone) is of interest in organic chemistry and may have potential applications in the synthesis of pharmaceuticals and other organic compounds due to its unique structure and reactivity.

348-15-2

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348-15-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 348-15-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,4 and 8 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 348-15:
(5*3)+(4*4)+(3*8)+(2*1)+(1*5)=62
62 % 10 = 2
So 348-15-2 is a valid CAS Registry Number.

348-15-2Downstream Products

348-15-2Relevant academic research and scientific papers

From Phenylhydrazone to 1H-1,2,4-Triazoles via Nitrification, Reduction and Cyclization

Hao, Liqiang,Wang, Guodong,Sun, Jian,Xu, Jun,Li, Hongshuang,Duan, Guiyun,Xia, Chengcai,Zhang, Pengfei

supporting information, p. 1657 - 1662 (2020/03/19)

Herein we report an annulation of phenylhydrazone via a tandem nitrification, reduction, cyclization protocol employing cobalt nitrate and 1,2-dichloroethane to produce substituted 1H-1,2,4-triazoles. Notably, 1,2-dichloroethane serves both the solvent and a hydrogen source for transfer hydrogenation. This methodology works under mild conditions, providing a direct approach for the synthesis of 1H-1,2,4-triazoles. (Figure presented.).

N-PHENYL-1,1,1-TRIFLUOROMETHANESULFONAMIDE HYDRAZONE DERIVATIVE COMPOUNDS AND THEIR USAGE IN CONTROLLING PARASITES

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Page/Page column 29, (2008/06/13)

Novel N-phenyl-1,1,1-trifluoromethanesulfonamide compounds useful for controlling endo and/or ectoparasites in the environment are provided, together with methods of making the same, and methods of using the inventive compounds to treat parasite infestations in vivo and ex vivo.

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