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(E)-1-cyclopropyl-3-(4-(trifluoromethyl)phenyl)prop-2-en-1-one is a complex organic compound characterized by a unique molecular structure. It features a cyclopropyl group attached to the 1st carbon, a trifluoromethylphenyl group at the 3rd position, and a prop-2-en-1-one functional group, which includes a carbonyl group and a double bond. This molecule is known for its potential applications in the synthesis of pharmaceuticals and agrochemicals due to its specific reactivity and structural properties. The presence of the trifluoromethyl group enhances the lipophilicity and metabolic stability of the compound, which can be beneficial in drug design. The cyclopropyl ring introduces a unique three-membered ring structure that can affect the molecule's conformation and interaction with biological targets. Overall, (E)-1-cyclopropyl-3-(4-(trifluoromethyl)phenyl)prop-2-en-1-one is of interest in the field of medicinal chemistry for its potential to be a precursor or a building block for more complex molecules with therapeutic or pesticidal properties.

72881-74-4

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72881-74-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72881-74-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,8,8 and 1 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 72881-74:
(7*7)+(6*2)+(5*8)+(4*8)+(3*1)+(2*7)+(1*4)=154
154 % 10 = 4
So 72881-74-4 is a valid CAS Registry Number.

72881-74-4Relevant academic research and scientific papers

Asymmetric transfer hydrogenation of cycloalkyl vinyl ketones to allylic alcohols catalyzed by ruthenium amido complexes

Liu, Sensheng,Cui, Peng,Wang, Juan,Zhou, Haifeng,Liu, Qixing,Lv, Jinliang

supporting information, p. 264 - 267 (2019/01/10)

A chemoselective 1,2-reduction of cycloalkyl vinyl ketones via asymmetric transfer hydrogenation is described. The reduction proceeded smoothly with a chiral diamine ruthenium complex as a catalyst and a HCOOH-NEt3 azeotrope as both a hydrogen source and solvent under mild conditions. A wide range of 1-cycloalkyl chiral allylic alcohols were obtained in good yields and up to 87% ee. It was found that the alkyl group plays an important role in the enantioselectivity.

PYRIDINE AND PYRIMIDINE DERIVATIVES AS MGIUR2 ANTAGONISTS

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Page/Page column 35, (2010/11/29)

The present invention relates to compounds of formula (I), a process for the manufacture thereof, pharmaceutical compositions containing them, and their use for treating CNS disorders:wherein A, B, X, Y, R1, R2, R3 and R4 are as defined in the description and claims.

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