23192-82-7 Usage
Description
(E)-9-Tetradecen-1-olacetate, also known as (9E)-Tetradecen-1-yl Acetate, is a bioactive component derived from Aglaia elaeagnoidea. It is a naturally occurring compound with a variety of potential therapeutic properties.
Uses
Used in Pharmaceutical Applications:
(E)-9-Tetradecen-1-olacetate is used as a therapeutic agent for its potential antitumor, analgesic, antihypertensive, and anti-inflammatory properties. It is believed to provide relief and treatment for various health conditions by targeting specific biological pathways and processes.
Used in Anticancer Applications:
In the field of oncology, (E)-9-Tetradecen-1-olacetate is used as an anticancer agent. It may help in the treatment of various types of cancer by modulating cellular processes and signaling pathways involved in tumor growth and progression.
Used in Pain Management:
As an analgesic, (E)-9-Tetradecen-1-olacetate is used to alleviate pain and discomfort associated with various conditions. Its natural origin and potential efficacy make it a promising candidate for the development of new pain management therapies.
Used in Cardiovascular Applications:
In the cardiovascular industry, (E)-9-Tetradecen-1-olacetate is used as an antihypertensive agent. It may help in the regulation of blood pressure and contribute to the overall management of hypertension-related health issues.
Used in Anti-inflammatory Applications:
(E)-9-Tetradecen-1-olacetate is also used as an anti-inflammatory agent, potentially providing relief from inflammation-related symptoms and conditions. Its natural properties make it a valuable component in the development of new anti-inflammatory medications and treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 23192-82-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,1,9 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 23192-82:
(7*2)+(6*3)+(5*1)+(4*9)+(3*2)+(2*8)+(1*2)=97
97 % 10 = 7
So 23192-82-7 is a valid CAS Registry Number.
InChI:InChI=1/C16H30O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-18-16(2)17/h6-7H,3-5,8-15H2,1-2H3/b7-6+
23192-82-7Relevant articles and documents
Insect sex attractants: XIV. All trans alkenol acetates via sodium liquid ammonia reduction
Warthen Jr,Jacobson
, p. 616 - 617 (1973)
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Preparation of 9-Alkenyl Ester Compounds
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, (2008/06/13)
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SYNTHESIS OF PHEROMONES, IV. CHEMISTRY OF THE WITTIG REACTION, I. EFFECTS OF REACTION CONDITIONS ON THE STEREOSELECTIVITY AND YIELD OF THE WITTIG REACTION
Vinczer, Peter,Juvancz, Zoltan,Novak, Lajos,Szantay, Csaba
, p. 797 - 820 (2007/10/02)
The reactions of nonstabilized triphenylphosphorus ylides with aldehydes have been studied in detail.The stereochemistry and yields of the alkene products are highly dependent upon base used for the generation of the ylide, the solvent and reaction temperature.The synthesis of sex pheromone components by Wittig reaction are also described.
