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3-(4-HYDROXY-PHENYL)-1H-PYRAZOLE-4-CARBALDEHYDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

879996-57-3

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879996-57-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 879996-57-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,9,9,9 and 6 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 879996-57:
(8*8)+(7*7)+(6*9)+(5*9)+(4*9)+(3*6)+(2*5)+(1*7)=283
283 % 10 = 3
So 879996-57-3 is a valid CAS Registry Number.

879996-57-3Downstream Products

879996-57-3Relevant academic research and scientific papers

Synthesis and biological evaluation of some pyrazole derivatives, containing (Thio) semicarbazide, as dual anti-inflammatory antimicrobial agents

Liang, Zhaochang,Huang, Yuping,Wang, Shiben,Deng, Xianqing

, p. 1020 - 1030 (2019/10/28)

Background: Several series of pyrazole derivatives containing (thio) semicarbazide (4a-4h, 5a-5l, 6a-6f, 7a-7c) were designed and synthesized to screen dual inflammatory and antimicrobial activities. Methods: The products were characterized by1

Structure-activity relationship study of a novel necroptosis inhibitor, necrostatin-7

Zheng, Weihong,Degterev, Alexei,Hsu, Emily,Yuan, Junying,Yuan, Chengye

scheme or table, p. 4932 - 4935 (2009/05/26)

Necroptosis is a regulated caspase-independent cell death mechanism characterized by morphological features resembling non-regulated necrosis. Necrotatin-7 (Nec-7), a novel potent small-molecule inhibitor of necroptosis, is structurally distinct from previously described necrostatins (Nec-1, Nec-3, Nec-4 and Nec-5). Here, we describe a series of structural modifications and the structure-activity relationship (SAR) of the Nec-7 series for inhibiting necroptosis.

Synthesis of 3-substituted arylpyrazole-4-carboxylic acids

Lebedev,Lebedeva,Sheludyakov,Kovaleva,Ustinova,Kozhevnikov

, p. 782 - 789 (2007/10/03)

A method was suggested for preparing previously unknown 3-aryl-substituted pyrazole-4-carboxylic acids, involving Vilsmeier formylation of semicarbazones of 26 available mono- and disubstituted acetophenones and 2-acetylthiophene followed by oxidation of

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