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(Z)-2-Methyl-3-(3-trifluoromethyl-phenyl)-but-2-enoic acid ethyl ester is a complex organic compound with the molecular formula C13H13F3O2. It is a derivative of but-2-enoic acid, featuring a methyl group at the 2nd carbon, a 3-trifluoromethyl-phenyl group at the 3rd carbon, and an ethyl ester group attached to the carboxylic acid. (Z)-2-Methyl-3-(3-trifluoromethyl-phenyl)-but-2-enoic acid ethyl ester is characterized by its (Z)-configuration, indicating the geometric arrangement of the double bond, with the highest priority substituents on the same side of the double bond. It is a colorless liquid with a fruity odor and is used in the fragrance industry to impart floral and fruity notes to perfumes and other scented products.

52094-30-1

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52094-30-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52094-30-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,0,9 and 4 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 52094-30:
(7*5)+(6*2)+(5*0)+(4*9)+(3*4)+(2*3)+(1*0)=101
101 % 10 = 1
So 52094-30-1 is a valid CAS Registry Number.

52094-30-1Relevant academic research and scientific papers

Structure-activity relationship in cinnamamides. 3. Synthesis and anticonvulsant activity evaluation of some derivatives of (E)- and (Z)-m-(trifluoromethyl)cinnamamide

Balsamo,Crotti,Lapucci,Macchia,Macchia,Cuttica,Passerini

, p. 525 - 532 (2007/10/02)

The (E)- and (Z)-m-(trifluoromethyl)-α,β-dimethylcinnamamides and some of their N-alkyl derivatives were prepared and pharmacologically tested as anticonvulsant agents in order to verify if a ring substituent, like the m-CF3 group, different from a halogen but possessing the same electronic effect could lead to equally active compounds. Some (E)-m-(trifluoromethyl)-α-methyl- and -non-methyl-substituted-cinnamamides were also prepared and tested. In the α,β-dimethyl series, the results show that the m-CF3 group leads to products more active than the ones unsubstituted on the phenyl ring but still less active than the p-halogen-substituted compounds previously studied. In the α-methyl and non-methyl-substituted series, the trend shows the m-CF3 group being able to produce less toxic and, in some cases, more active products than the previously studied amides.

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