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5-Hydroxy-1-phenyl-1H-pyrazole-3-acetic acid is a chemical compound with the molecular formula C11H10N2O3. It is a derivative of pyrazole, a heterocyclic organic compound consisting of a five-membered aromatic ring with two nitrogen atoms and three carbon atoms. The presence of a hydroxyl group (-OH) at the 5-position and a phenyl group (C6H5) at the 1-position, along with an acetic acid moiety (-CH2COOH) at the 3-position, gives 5-hydroxy-1-phenyl-1H-Pyrazole-3-acetic acid unique properties and potential applications in various fields, such as pharmaceuticals and agrochemicals. Its structure and functional groups contribute to its reactivity and interactions with other molecules, making it a subject of interest for researchers in organic chemistry and related disciplines.

52546-46-0

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52546-46-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52546-46-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,5,4 and 6 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 52546-46:
(7*5)+(6*2)+(5*5)+(4*4)+(3*6)+(2*4)+(1*6)=120
120 % 10 = 0
So 52546-46-0 is a valid CAS Registry Number.

52546-46-0Relevant academic research and scientific papers

Synthesis of 3-(2-aminoethyl)-5-hydroxy-1H-pyrazole derivatives

Groselj, Uros,Kralj, David,Wagger, Jernej,Dahmann, Georg,Stanovnik, Branko,Svete, Jurij

experimental part, p. 49 - 65 (2012/03/11)

Treatment of β-keto ester 8 with hydrazines 9a-g gave 1'-substituted tert-butyl 2-(5-hydroxy-1Hpyrazol- 3-yl)ethylcarbamates 10a-e and 2-(5-oxo-2,5-dihydro-1H-pyrazol-3-yl)ethylcarbamates 11f,g. Acidolytic deprotection of 10b,c afforded the corresponding 3-(2-aminoethyl)-5-hydroxy- 1H-pyrazoles 6b,c in good yields. Acylation of 6 gave either the N-acyl compounds 12b,c and 13c, or the N,O-diacyl derivative 14. Next, three N,N-dialkyl analogues 15a,b and 26c were prepared from dimethyl acetone-1,3-dicarboxylate 21 via condensation with hydrazines 9a and 9h followed by hydrolysis of the esters 22a,b, amidation of the carboxylic acids 23a,b, and reduction of the tertiary carboxamides 24a and 25b,c. ARKAT-USA, Inc.

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