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1H-Pyrazole-3-carbonitrile, 4-benzoyl-1-methyl-5-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

851083-46-0

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851083-46-0 Usage

Chemical structure

1H-Pyrazole-3-carbonitrile, 4-benzoyl-1-methyl-5-phenyl-

Type of compound

Pyrazole derivative

Functional groups

Carbonitrile, benzoyl, methyl substituent

Usage

Organic synthesis, pharmaceutical research, as an intermediate in the preparation of pharmaceutical drugs and related compounds

Unique features

Useful for a variety of chemical reactions and applications in the field of medicinal chemistry and drug development due to its unique structure and chemical properties.

Check Digit Verification of cas no

The CAS Registry Mumber 851083-46-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,1,0,8 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 851083-46:
(8*8)+(7*5)+(6*1)+(5*0)+(4*8)+(3*3)+(2*4)+(1*6)=160
160 % 10 = 0
So 851083-46-0 is a valid CAS Registry Number.

851083-46-0Downstream Products

851083-46-0Relevant academic research and scientific papers

Synthesis and antibacterial activity of 4-benzoyl-1-methyl-5-phenyl-1H- pyrazole-3-carboxylic acid and derivatives

Akbas, Esvet,Berber, Ismet,Sener, Ahmet,Hasanov, Beybala

, p. 23 - 26 (2007/10/03)

Some new 1H-pyrazole-3-carboxylic acid and pyridazinone derivatives were synthesized and evaluated for their antibacterial activities against Bacillus cereus ATCC 7064, Staphylococcus aureus ATCC 6538, Escherichia coli ATCC 4230 and Pseudomonas putida usi

Antibacterial and antifungal activities of new pyrazolo[3,4-d]pyridazin derivatives

Akbas, Esvet,Berber, Ismet

, p. 401 - 405 (2007/10/03)

Several new pyrazolo[3,4-d]pyridazin derivatives were prepared by the reaction of two new 1H-pyrazole-3-carboxylic acids and various hydrazines. The compounds were tested for antimicrobial activities against Gram-negative, Gram-positive bacteria and fungi

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