15601-09-9 Usage
Uses
Used in Fragrance and Flavor Industry:
2-Heptanone, 1-(3,5-dihydroxyphenyl)is used as a key ingredient in the fragrance and flavor industry for its distinct floral scent that resembles violets. It is incorporated into a variety of products such as perfumes, soaps, and cosmetics to enhance their olfactory appeal.
Used in Antioxidant Applications:
2-Heptanone, 1-(3,5-dihydroxyphenyl)is studied for its potential antioxidant properties, which can help protect cells from damage caused by free radicals. This makes it a valuable compound in the development of products that promote health and wellness.
Used in Anti-Inflammatory Applications:
2-Heptanone, 1-(3,5-dihydroxyphenyl)is also being researched for its possible anti-inflammatory effects, which could be beneficial in the creation of treatments for various inflammatory conditions. This application further broadens the scope of its use in the pharmaceutical and healthcare sectors.
Used in Cosmetics Industry:
In the cosmetics industry, 2-Heptanone, 1-(3,5-dihydroxyphenyl)is used as a fragrance ingredient to provide a pleasant scent to products. Its floral aroma adds a desirable quality to cosmetics, enhancing the sensory experience for consumers.
Used in Perfumery:
As a significant component in perfumes, 2-Heptanone, 1-(3,5-dihydroxyphenyl)contributes to the complex and long-lasting scents that are characteristic of high-quality perfumes. Its ability to evoke the scent of violets makes it a sought-after ingredient in the art of perfume making.
Check Digit Verification of cas no
The CAS Registry Mumber 15601-09-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,6,0 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 15601-09:
(7*1)+(6*5)+(5*6)+(4*0)+(3*1)+(2*0)+(1*9)=79
79 % 10 = 9
So 15601-09-9 is a valid CAS Registry Number.
15601-09-9Relevant academic research and scientific papers
Synthesis of further β-ketoalkyl lichen depsides
Elix, John A.,Wardlaw, Judith H.
, p. 479 - 486 (2007/10/03)
The unambiguous total synthesis of the lichen depsides 2-O-methylglomelliferic acid (39), 4-O-methylhyperolivetoric acid (40), hyperconfluentic acid (41), microphyllinic acid (42), arthoniaic acid (43), 2′-O-methylmicrophyllinic acid (44), 2′-O-methylhype
