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1H-Pyrazolo[4,3-c]pyridine, 3-methyl-6-(trifluoromethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

340809-54-3

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340809-54-3 Usage

Structure

Pyrazolopyridine derivative with a trifluoromethyl group at the 6th position and a methyl group at the 3rd position

Known for

Potential pharmacological and biological activities

Common use

Building block in the synthesis of pharmaceutical compounds and other organic molecules

Suitability

For use in drug development and medicinal chemistry research

Unique feature

Trifluoromethyl group contributes to its unique chemical reactivity and physical properties, making it a valuable tool in the field of organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 340809-54-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,0,8,0 and 9 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 340809-54:
(8*3)+(7*4)+(6*0)+(5*8)+(4*0)+(3*9)+(2*5)+(1*4)=133
133 % 10 = 3
So 340809-54-3 is a valid CAS Registry Number.

340809-54-3Downstream Products

340809-54-3Relevant academic research and scientific papers

Synthesis of 5-alkyl-4-amino-2-(trifluoromethyl)pyridines and their transformation into trifluoromethylated 1H-pyrazolo[4,3-c]pyridines

Tyvorskii, Vladimir I,Bobrov, Denis N,Kulinkovich, Oleg G,Tehrani, Kourosch Abbaspour,Kimpe, Norbert De

, p. 2051 - 2055 (2001)

5-Alkyl-4-amino-2-(trifluoromethyl)pyridines were prepared in good yields starting from the corresponding pyridinols either using condensation with tosyl isocyanate or by alkylation with 2-chloroacetamide and subsequent Smiles type rearrangement. The cyclisation of diazonium salts, generated from 5-alkyl-4-amino-2-(trifluoromethyl)pyridines, afforded trifluoromethylated 1H-pyrazolo[4,3-c]pyridines.

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