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1-phenyl-4-phenylsulfonyl-5-p-tolyl-1H-pyrazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1043391-50-9

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1043391-50-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1043391-50-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,3,3,9 and 1 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1043391-50:
(9*1)+(8*0)+(7*4)+(6*3)+(5*3)+(4*9)+(3*1)+(2*5)+(1*0)=119
119 % 10 = 9
So 1043391-50-9 is a valid CAS Registry Number.

1043391-50-9Upstream product

1043391-50-9Downstream Products

1043391-50-9Relevant academic research and scientific papers

Synthesis and analgesic/anti-inflammatory evaluation of fused heterocyclic ring systems incorporating phenylsulfonyl moiety

Shaaban, Mohamed R.,Saleh, Tamer S.,Mayhoub, Abdelrahman S.,Mansour, Ahmed,Farag, Ahmad M.

, p. 6344 - 6352 (2008)

A series of pyrazolo[1,5-a]pyrimidine, triazolo[1,5-a]pyrimidine, and pyrimido[1,2-a]benzimidazole ring systems incorporating phenylsulfonyl moiety were synthesized via the reaction of 3-(N,N-dimethylamino)-1-aryl-2-(phenylsulfonyl)prop-2-en-1-one derivatives 2a,b with appropriate nitrogen nucleophiles. The analgesic and anti-inflammatory activities of the newly synthesized compound were investigated in vivo. 3-Bromo-2-phenyl-6-(phenylsulfonyl)-7-(4-methylphenyl)pyrazolo[1,5-a]pyrimidine (5e) was found to have an excellent analgesic activity in comparison with indomethacin as a reference drug, while the highest anti-inflammatory effect was observed in the case of 2-(4-bromophenyl)-6-(phenylsulfonyl)-5-(4-methylphenyl)pyrazolo[1,5-a]pyrimidine (5d). From the structure-activity relationship (SAR) point of view, the analgesic/anti-inflammatory activity of pyrazolo[1,5-a]pyrimidine derivatives was found to be much higher than triazolo[1,5-a]pyrimidine and pyrimido[1,2-a]benzimidazole derivatives.

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