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86238-93-9

(Z)-3-(4-carbethoxy-2-fluorophenyl)-2-methylpropenal is a complex organic compound characterized by its unique molecular structure. It is a conjugated aldehyde with a fluorophenyl group, which contributes to its distinct chemical properties. The molecule features a 2-methylpropenal backbone, which is a three-carbon chain with a double bond between the second and third carbon atoms, and a methyl group attached to the second carbon. The 4-carbethoxy-2-fluorophenyl group is attached to the third carbon of the aldehyde, with the carbethoxy group (ester of acetic acid) providing additional functionality. (Z)-3-(4-carbethoxy-2-fluorophenyl)-2-methylpropenal is of interest in the field of organic chemistry, potentially for its reactivity and applications in the synthesis of more complex molecules. Its specific properties and uses would depend on the context in which it is being studied or applied.

86238-93-9

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86238-93-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86238-93-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,2,3 and 8 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 86238-93:
(7*8)+(6*6)+(5*2)+(4*3)+(3*8)+(2*9)+(1*3)=159
159 % 10 = 9
So 86238-93-9 is a valid CAS Registry Number.

86238-93-9Relevant articles and documents

Aromatic retinoic acid analogues

-

, (2008/06/13)

Aromatic retinoic acid analogues of the formula STR1 where X is hydrogen or fluorine, Y is hydrogen, halogen of atomic number 9 or 17, hydroxy, alkyl of 1 to 2 carbon atoms or alkoxy of 1 to 2 carbon atoms and R is hydroxy, alkoxy, aroxy, or NR 1 R 2 where R 1 is hydrogen, alkyl, or aryl and R 2 is alkyl or aryl, with the proviso that when Y is hydrogen, X is fluorine. These retinoids are useful as chemopreventive agents for inhibiting tumor promotion in epithelial cells and for treating nonmalignant skin disorders.

Aromatic Retinoic Acid Analogues. 2. Synthesis and Pharmacological Activity

Dawson, Marcia I.,Chan, Rebecca,Hobbs, Peter D.,Chao, Wan-ru,Schiff, Leonard J.

, p. 1282 - 1293 (2007/10/02)

Aromatic analogues of (E)-1-(4-carboxyphenyl)-2-methyl-4-(2,6,6-trimethyl-1-cyclohexen-1-yl)butadiene (1b) and its ethyl ester (1a) were synthesized as potential chemopreventive agents for the treatment of epithelial cancer and such skin diseases as psoriasis and cystic acne.The phenyl ring of 1 was replaced by 2-fluorophenyl, 2-methoxyphenyl, thienyl, furanyl, and pyridyl groups.The 1-fluorobutadiene analogue of 1 was also synthesized.With exception for the furanyl analogue, these compounds demonstrated good activity in reversing keratinization in hamster tracheal organ culture and in inhibiting the induction of ornithine decarboxylase in mouse epidermis by a tumor promoter.

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