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2-(2,4-dichlorophenyl)pent-4-enoic acid is a chemical compound with the molecular formula C11H10Cl2O2. It is an organic compound that features a pent-4-enoic acid backbone, which is a five-carbon chain with a double bond between the fourth and fifth carbon atoms, and a 2,4-dichlorophenyl group attached to the second carbon. The presence of two chlorine atoms at the 2nd and 4th positions of the phenyl ring gives 2-(2,4-dichlorophenyl)pent-4-enoic acid unique properties. It is a colorless to pale yellow solid and is used in the synthesis of various pharmaceuticals and agrochemicals due to its potential biological activity. The compound is also known for its role as an intermediate in the production of certain herbicides, highlighting its importance in the chemical industry.

2535-08-2

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2535-08-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2535-08-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,3 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2535-08:
(6*2)+(5*5)+(4*3)+(3*5)+(2*0)+(1*8)=72
72 % 10 = 2
So 2535-08-2 is a valid CAS Registry Number.

2535-08-2Relevant academic research and scientific papers

BICYCLIC COMPOUNDS FOR THE REDUCTION OF BETA-AMYLOID PRODUCTION

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Page/Page column 65, (2010/08/08)

The present disclosure provides a series of compounds of the formula (I) which reduce β-amyloid peptide (β-AP) production and are useful in the treatment of Alzheimer's Disease and other conditions affected by β-amyloid peptide (β-AP) production, wherein

Synthesis and structure-antifungal activity relationships of 3-aryl-5-alkyl-2,5-dihydrofuran-2-ones and their carbanalogues: Further refinement of tentative pharmacophore group

Pour, Milan,Spulak, Marcel,Balsanek, Vojtech,Kunes, Jiri,Kubanova, Petra,Buchta, Vladimir

, p. 2843 - 2866 (2007/10/03)

Two series of 3-(substituted phenyl)-5-alkyl-2,5-dihydrofuran-2-ones related to a natural product, (-)incrustoporine, were synthesized and their in vitro antifungal activity evaluated. The compounds with halogen substituents on the phenyl ring exhibited selective antifungal activity against the filamentous strains of Absidia corymbifera and Aspergillus fumigatus. On the other hand, the influence of the lenghth of the alkyl chain at C(5) was marginal. The antifungal effect of the most active compound against the above strains was higher than that of ketoconazole, and close to that of amphotericin B. In order to verify the hypothesis about a possible relationship between the Michael-accepting ability of the compounds and their antifungal activity, a series of simple carbanalogues, 2-(substituted phenyl)cyclopent-2-enones, was prepared and subjected to antifungal activity assay as well.

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