533-24-4 Usage
Description
4-Pentylresorcinol, also known as 4-pentyl-1,3-benzenediol, is a chemical compound with a unique structure that features a resorcinol core with a pentyl chain attached. It is known for its potential applications in various fields, particularly in biological studies and pharmaceutical research.
Uses
Used in Biological Studies:
4-Pentylresorcinol is used as a research compound for studying the mechanism-based inhibition of recombinant human cytochrome P450 1A1. This application is significant in understanding the enzyme's role in drug metabolism and its potential interactions with other substances.
Used in Pharmaceutical Research:
4-Pentylresorcinol is used as a starting material or intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and properties make it a valuable candidate for the development of new drugs with potential therapeutic applications.
Used in Chemical Synthesis:
4-Pentylresorcinol can be used as a building block in the synthesis of more complex organic molecules. Its versatility in chemical reactions allows it to be a valuable component in the creation of novel compounds with diverse applications.
Check Digit Verification of cas no
The CAS Registry Mumber 533-24-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,3 and 3 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 533-24:
(5*5)+(4*3)+(3*3)+(2*2)+(1*4)=54
54 % 10 = 4
So 533-24-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H16O2/c1-2-3-4-5-9-6-7-10(12)8-11(9)13/h6-8,12-13H,2-5H2,1H3
533-24-4Relevant articles and documents
Antifungal Activity of 2,4-Dihydroxyacylophenones and Related Compounds
Mizobuchi, Shigeyuki,Sato, Yuko
, p. 1327 - 1334 (2007/10/02)
The antifungal activity of 2,4-dihydroxyacylophenones and related compounds against Trichophyton spp. and other fungi were investigated to determine their structure-activity relationships.The activity of these compounds was found to be closely related to the length of the acyl and alkyl substituents attached to the 1,3-dihydroxybenzene moiety.In addition, differences in activity were observed depending on the position of the alkyl substituents and on the number of substituents attached to the 1,3-dihydroxybenzene moiety.Some compounds tested showed potent antifungal activity against Trichophyton spp. and other fungi that was more active than amphotericin B.