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1-(Trifluoromethyl)-9H-carbazole is a chemical compound with the molecular formula C13H8F3N and a molecular weight of 233.21 g/mol. It is a derivative of carbazole, a tricyclic aromatic compound, with a trifluoromethyl group (-CF3) attached to the 1-position of the carbazole ring. 1-(trifluoromethyl)-9H-carbazole is known for its potential applications in the synthesis of various pharmaceuticals, agrochemicals, and materials science due to its unique electronic and steric properties. The trifluoromethyl group imparts increased lipophilicity and metabolic stability to the molecule, which can be beneficial in drug design. Additionally, 1-(trifluoromethyl)-9H-carbazole may be used as an intermediate in the preparation of more complex molecules, showcasing its versatility in organic synthesis.

3904-47-0

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3904-47-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3904-47-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,0 and 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3904-47:
(6*3)+(5*9)+(4*0)+(3*4)+(2*4)+(1*7)=90
90 % 10 = 0
So 3904-47-0 is a valid CAS Registry Number.

3904-47-0Downstream Products

3904-47-0Relevant academic research and scientific papers

A direct palladium-catalyzed route to selectively substituted carbazoles through sequential C-C and C-N bond formation: Synthesis of carbazomycin A

Della Ca', Nicola,Sassi, Giovanni,Catellani, Marta

supporting information; experimental part, p. 2179 - 2182 (2009/10/02)

The present paper offers a synthetically simple one-pot procedure for the catalytic preparation of the biologically interesting class of carbazoles. The new procedure is based on the combined catalysis of palladium and norbornene starting from o-substituted iodoarenes and N-sulfonylated or N-acetylated o-bromoanilines. A well-known member of this class, carbazomycin A, has been successfully prepared.

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