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Benzeneacetamide, N-[2-(trifluoromethyl)phenyl]-, also known as 2-(Trifluoromethyl)benzeneacetamide, is an organic compound with the chemical formula C9H8F3NO. It is a derivative of benzeneacetamide, featuring a trifluoromethyl group attached to the 2-position of the benzene ring. Benzeneacetamide, N-[2-(trifluoromethyl)phenyl]- is characterized by its molecular weight of 203.16 g/mol and a melting point of 90-92°C. It is a white to off-white crystalline solid and is soluble in organic solvents such as ethanol and acetone. The compound is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly those involving the trifluoromethyl group, which can enhance the lipophilicity and metabolic stability of the final product.

3829-42-3

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3829-42-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3829-42-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,2 and 9 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3829-42:
(6*3)+(5*8)+(4*2)+(3*9)+(2*4)+(1*2)=103
103 % 10 = 3
So 3829-42-3 is a valid CAS Registry Number.

3829-42-3Downstream Products

3829-42-3Relevant academic research and scientific papers

Synthesis of polysubstituted 4-fluoroquinolinones

Kiselyov, Alexander S.,Piatnitski, Evgueni L.,Doody, Jacqueline

, p. 4061 - 4063 (2004)

(Chemical Equation Presented) A convenient one-pot synthesis of 4-fluoroquinolinones that are active against KDR kinase is described. The mechanism of the reaction is believed to involve the formation of a quinone methide intermediate.

Quinoline-3-carboxamides

-

, (2008/06/13)

Novel quinoline-3-carboxamides of the formula STR1 wherein R1 is in the 5,6,7 or 8-position and is selected from the group consisting of hydrogen, halogen, --CF3, --OCF3, --SCF3, straight chain alkyl of 1 to 4 carbon atoms, branched alkyl of 3 to 5 carbon atoms and alkoxy of 1 to 4 carbon atoms, R2 is selected from the group consisting of hydrogen and methyl, R3 is selected from the group consisting of thiazolyl, 4,5-dihydrothiazolyl, pyridinyl, oxazolyl and imidazolyl and R4 is selected from the group consisting of hydrogen, hydroxyl, alkyl of 1 to 4 carbon atoms, phenyl and benzyl with the proviso that when R1 is in the 7 or 8-position and is halogen, --CH3, --OCF3 or --SCF3 and R4 is hydrogen, R3 is not thiazolyl, pyridinyl or oxazolyl and the non-toxic, pharmaceutically acceptable acid addition salts when R3 is imidazolyl or 4,5-dihydrothiazolyl having analgesic activity and their preparation and novel intermediates therefore.

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