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(1-ethyl-3-methyl-1H-pyrazol-4-yl)(phenyl)methanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1007519-47-2

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1007519-47-2 Usage

General Description

The chemical (1-ethyl-3-methyl-1H-pyrazol-4-yl)(phenyl)methanone, also known as Ethyl 3-methyl-1H-pyrazole-4-carboxylate, is a yellowish liquid with a molecular formula C14H14N2O and a molecular weight of 226.27 g/mol. It is used as a starting material in chemical synthesis and has potential applications in pharmaceuticals and agrochemicals. (1-ethyl-3-methyl-1H-pyrazol-4-yl)(phenyl)methanone has a pyrazole ring, an ethyl group, a methyl group, and a phenyl group, which makes it highly versatile for creating a wide variety of molecules with potentially useful properties. Additionally, it has been reported to have antioxidant and antimicrobial activities, which could make it valuable for various industrial and medical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1007519-47-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,7,5,1 and 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1007519-47:
(9*1)+(8*0)+(7*0)+(6*7)+(5*5)+(4*1)+(3*9)+(2*4)+(1*7)=122
122 % 10 = 2
So 1007519-47-2 is a valid CAS Registry Number.

1007519-47-2Downstream Products

1007519-47-2Relevant academic research and scientific papers

Direct electrophilic acylation of n-substituted pyrazoles by anhydrides of carboxylic acids

Taydakov, Ilya V.,Krasnoselskiy, Sergey S.

, p. 2188 - 2192 (2013)

A simple, convenient and scalable approach to 1-substituted 4-acylpyrazoles through direct acylation of pyrazoles by anhydrides of aliphatic, aromatic and fluorinated carboxylic acids in the presence of concentrated sulfuric acid as a catalyst is described. Target ketones were obtained in 41-86% isolated yields in high purity without laborious purification. The scope and limitations of the method are discussed.

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