18979-65-2 Usage
Uses
Used in Organic Chemistry Research:
4-heptylbenzene-1,3-diol is used as a research compound for investigating its chemical properties and potential reactions due to its unique structure, which includes a benzene ring and two hydroxyl groups.
Used in Industrial Manufacturing:
4-heptylbenzene-1,3-diol is used as an intermediate or raw material in the synthesis of various industrial products, leveraging its aromatic and hydroxyl functional groups for specific chemical transformations.
Used in Pharmaceutical Development:
4-heptylbenzene-1,3-diol is used as a potential lead compound in drug discovery, with its structure offering opportunities for modification and optimization to target specific biological pathways or receptors.
Used in Material Science:
4-heptylbenzene-1,3-diol is used as a component in the development of new materials, such as polymers or coatings, where its aromatic and hydroxyl groups could contribute to desired properties like adhesion, stability, or reactivity.
Note: Since 4-heptylbenzene-1,3-diol is not a well-known compound, it is essential to take necessary precautions when handling or using it in any application. Further research and development are required to fully understand its potential uses and benefits.
Check Digit Verification of cas no
The CAS Registry Mumber 18979-65-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,9,7 and 9 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 18979-65:
(7*1)+(6*8)+(5*9)+(4*7)+(3*9)+(2*6)+(1*5)=172
172 % 10 = 2
So 18979-65-2 is a valid CAS Registry Number.
18979-65-2Relevant academic research and scientific papers
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.
