77327-13-0 Usage
Uses
Used in Fragrance and Flavor Industry:
Octacosan-2-one is utilized as a key component in the preparation of organoleptic compounds, specifically in the fragrance and flavor industry. Its unique properties contribute to the development of various scents and tastes, making it a valuable asset in creating appealing products for consumers.
Used in Organic Chemistry Research:
octacosan-2-one is also frequently found in chemistry laboratories, where it is used in the field of organic chemistry. Researchers leverage octacosan-2-one for various experiments and studies, furthering the understanding of its chemical properties and potential applications in different areas of science.
Used in Health Supplements:
Although primarily known for its applications in fragrances and flavors, octacosan-2-one shares a close relationship with octacosanol, which is used in health supplements. This connection suggests that octacosan-2-one may also have potential uses in the development of health products, particularly those aimed at improving physical performance and endurance. However, further research would be required to explore and validate these potential applications.
Check Digit Verification of cas no
The CAS Registry Mumber 77327-13-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,3,2 and 7 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 77327-13:
(7*7)+(6*7)+(5*3)+(4*2)+(3*7)+(2*1)+(1*3)=140
140 % 10 = 0
So 77327-13-0 is a valid CAS Registry Number.
77327-13-0Relevant academic research and scientific papers
Synthesis of racemic and each enantiomer of 3-methylnonacosanol, a new plant growth regulator from Lowsonia inermis
Kulkarni, Bheemashankar A.,Sankaranarayanan, Sivaraman,Subbaraman, Ayalur S.,Chattopadhyay, Subrata
, p. 1571 - 1577 (2007/10/03)
An efficient synthesis of the title compound I in racemic and enantiomeric forms has been developed starting from 10-undecenoic acid. For the enantiomeric synthesis, a lipase catalyzed acylation strategy was employed to prepare the required methyl branched chiron which was subsequently derivatized to give the enantiomers of I. The plant growth regulatory (PGR) assay of I, carried out with hypocotyl cuttings of French beans (Phaseolus vulgaris L.) in Steinberg's nutrient medium revealed appreciable activity at a concentration of 2.5 ppm. The PGR activities of the compound both in racemic and enantiomeric forms were better than 1- triacontanol, the enantiomer, (S)-I being the best test candidate.
