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1H-Pyrazole,3-ethoxy-5-(trifluoromethyl)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

676487-70-0

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676487-70-0 Usage

Compound type

1H-Pyrazole derivative

Contains

Trifluoromethyl group, Ethoxy group

Potential properties

Pharmacological and biological activities

Possible applications

Medicinal chemistry, Drug discovery research

Note

Further studies needed to understand properties and potential applications in the pharmaceutical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 676487-70-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,6,4,8 and 7 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 676487-70:
(8*6)+(7*7)+(6*6)+(5*4)+(4*8)+(3*7)+(2*7)+(1*0)=220
220 % 10 = 0
So 676487-70-0 is a valid CAS Registry Number.

676487-70-0Relevant academic research and scientific papers

Alkoxypyrazoles and the process for their preparation

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Page/Page column 11; 15, (2010/03/02)

The present invention relates to a alkoxypyrazoles preparation process, and new alkoxypyrazole compounds.

An improved preparation of 3-alkoxypyrazoles

Guillou, Sandrine,Bonhomme, Frederic J.,Janin, Yves L.

experimental part, p. 3504 - 3508 (2009/05/09)

The condensation between alkyl acetoacetates and hydrazines constitutes the very well-known Knorr synthetic method leading to pyrazol-3/5-ones. However, contemporary reports describe an alternate reaction pathway leading to low yields of 3/5-alkoxypyrazoles using hydrazine salts. No general method for the selective synthesis of 3-alkoxypyrazoles has been reported to date, hence we focused on this side reaction in an attempt to turn it into the main transformation. Depending on the starting material, various 3-alkoxypyrazoles (methoxy, ethoxy, benzyloxy, isopropoxy, allyloxy) were obtained in up to 56% yield. Georg Thieme Verlag Stuttgart.

Synthesis of novel 3-amino-5-trifluoromethylazoles: A convenient method of obtaining N-(azol-3-yl)amines

Martins, Marcos A. P.,Cunico, Wilson,Brondani, Sergio,Peres, Rodrigo L.,Zimmermann, Nilo,Rosa, Fernanda A.,Fiss, Gabriela F.,Zanatta, Nilo,Bonacorso, Helio G.

, p. 1485 - 1493 (2007/10/03)

A convenient method to obtain 10 3-amino-5-trifluoromethyl-5-hydroxy-4,5- dihydroisoxazoles and 18 3-amino-5-trifluoromethyl-1H-pyrazoles by cyclocondensation reaction of 4-amino-4-ethoxy-1,1,1,-trifluorobut-3-en-2-ones [CF3COCH=C(OEt)NHR, wher

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