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4-chlorobenzophenone (diphenylacetyl)hydrazone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

92806-48-9

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92806-48-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92806-48-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,8,0 and 6 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 92806-48:
(7*9)+(6*2)+(5*8)+(4*0)+(3*6)+(2*4)+(1*8)=149
149 % 10 = 9
So 92806-48-9 is a valid CAS Registry Number.

92806-48-9Downstream Products

92806-48-9Relevant academic research and scientific papers

Reactions of 2-Diazo-1,2-Diphenylethanone and Diphenyldiazomethane with Ketohydrazones

Singh, Giria Shankar,Singh, Surendra Bahadur,Mehrotra, Kailash Nath

, p. 1667 - 1670 (1984)

The reactions of 2-diazo-1,2-diphenylethanone (1) with ketohydrazones (3a-c) in equimolecular ratio yield (diphenylacetyl)hydrazones (4a-c) of the corresponding benzophenones which on further treatment with 1 in equimolecular ratio leads to 1-diphenylacetylazo-1,1,3,3-tetraaryl-2-propanones (5a-c).The product 5a is also obtained in the reaction of 1 with benzophenone hydrazone (3a) in 2:1 molecular ratio.The bis(acetylacetonato)copper(II)-catalyzed reaction of 1 and also of diphenyldiazomethane (2) with ketohydrazones (3) affords ketazines (6).The mechanistic route for the formation of products is discussed.

Evaluation of some classical hydrazones of ketones and 1,2-diketones as antileishmanial, antibacterial and antifungal agents

Al-Kahraman, Yasser M.S.A.,Yasinzai, Masoom,Singh, Girija S.

experimental part, p. 1009 - 1013 (2012/10/08)

The paper describes the synthesis and antimicrobial (antileishmanial, antibacterial and antifungal) activity of some classical hydrazones of benzophenones and of 1,2-diketones. N-(Diaryl) acyl derivatives of these hydrazones have also been synthesized and evaluated. 4,4,- Demthoxybenzil monohydrazone and 4,4'-dimethoxybenzophenone hydrazone showed significant antileishmanial activity. The effect of substituents on the bioactivity is discussed.

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