2999-14-6 Usage
Uses
Used in Pharmaceutical Industry:
1-Pentanone, 4-methyl-1-(2,4,6-trihydroxyphenyl)is used as an active pharmaceutical ingredient for its potential anti-inflammatory and anti-cancer properties. Its antioxidant nature contributes to the development of medications that can combat oxidative stress-related diseases and conditions.
Used in Food Additive Industry:
In the food additive industry, 1-Pentanone, 4-methyl-1-(2,4,6-trihydroxyphenyl)is utilized as a natural antioxidant to extend the shelf life of food products and protect them from oxidative damage, ensuring freshness and quality.
Used in Cosmetic Products:
1-Pentanone, 4-methyl-1-(2,4,6-trihydroxyphenyl)is employed in cosmetic products for its antioxidant properties, which can help protect the skin from environmental stressors and promote overall skin health. Its potential anti-inflammatory effects may also contribute to soothing and calming formulations for sensitive skin types.
Research and Development:
1-Pentanone, 4-methyl-1-(2,4,6-trihydroxyphenyl)is a subject of ongoing research in the medical and scientific communities due to its potential therapeutic applications. Further studies are being conducted to explore its efficacy in treating various diseases and conditions, particularly in the areas of inflammation and cancer.
Check Digit Verification of cas no
The CAS Registry Mumber 2999-14-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,9 and 9 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2999-14:
(6*2)+(5*9)+(4*9)+(3*9)+(2*1)+(1*4)=126
126 % 10 = 6
So 2999-14-6 is a valid CAS Registry Number.
2999-14-6Relevant academic research and scientific papers
Antifungal Activities of 2,4,6-Trihydroxyacylophenones and Related Compounds
Mizobuchi, Shigeyuki,Sato, Yuko
, p. 719 - 724 (2007/10/02)
The antifungal activities of sixty two 2,4,6-trihydroxyacylophenones and related compounds against Trichophyton spp. and other fungi were investigated to study their structure-activity relationship.It was found that the activities of these compounds were closely related to the length of the acyl and alkyl chains attached to the 1,3,5-trihydroxybenzene moiety.Among the compounds tested, 2,4,6-trihydroxy-3-nonylacetophenone (V-7) showed the highest activity against Trichophyton spp., with MICs being 1.57 μg/ml, and was more active than amphotericin B.
