56401-30-0 Usage
Description
9,12-Octadecadien-1-ol, 4-methylbenzenesulfonate, (9Z,12Z)is a chemical compound with the molecular formula C24H40O3S. It is characterized by the presence of two double bonds at the 9th and 12th carbon atoms, which are in the Z configuration. 9,12-Octadecadien-1-ol, 4-methylbenzenesulfonate, (9Z,12Z)also features a hydroxyl group at the 1st carbon and a 4-methylbenzenesulfonate group attached to it. This structure gives it unique properties and makes it suitable for various applications in different industries.
Uses
Used in Chemical Synthesis:
9,12-Octadecadien-1-ol, 4-methylbenzenesulfonate, (9Z,12Z)is used as an intermediate in the synthesis of various chemical compounds. Its unique structure allows it to be a valuable building block for the creation of more complex molecules with specific properties and applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 9,12-Octadecadien-1-ol, 4-methylbenzenesulfonate, (9Z,12Z)is used as a precursor for the development of new drugs. Its chemical structure can be modified to create compounds with potential therapeutic applications, such as anti-inflammatory, analgesic, or anti-cancer agents.
Used in Food Industry:
9,12-Octadecadien-1-ol, 4-methylbenzenesulfonate, (9Z,12Z)is used as an intermediate in the synthesis of Ethyl 11,14-Diepoxyeicosanoate (E916000), which is a standard used to determine epoxidized soybean oil in foods. This application helps ensure the quality and safety of food products containing epoxidized soybean oil.
Used in Cosmetics Industry:
In the cosmetics industry, 9,12-Octadecadien-1-ol, 4-methylbenzenesulfonate, (9Z,12Z)can be used as a component in the formulation of various cosmetic products. Its unique properties may contribute to the development of products with improved skin hydration, anti-aging, or anti-inflammatory effects.
Used in Research and Development:
9,12-Octadecadien-1-ol, 4-methylbenzenesulfonate, (9Z,12Z)is also used in research and development for the study of its chemical properties and potential applications. This can lead to the discovery of new compounds and technologies that can benefit various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 56401-30-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,4,0 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 56401-30:
(7*5)+(6*6)+(5*4)+(4*0)+(3*1)+(2*3)+(1*0)=100
100 % 10 = 0
So 56401-30-0 is a valid CAS Registry Number.
56401-30-0Relevant articles and documents
Cationic lipid compound and its preparation method
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Paragraph 0025; 0027, (2017/07/11)
The invention discloses cationic lipid compounds and a preparation method thereof. The molecular structure general formula of the compounds is shown as the description, wherein R is alkyl groups of C6 to C24, alkylenes of C6 to C24 and acyl groups of C6 t
Synthesis of phosphatidylcholine having a very long chain polyunsaturated fatty acid
Haider, Syed Shabbir,Tanaka, Masatoshi,Alam, Md Khorshed,Nakajima, Shuhei,Baba, Naomichi,Shimizu, Sakayu
, p. 175 - 176 (2007/10/03)
A phosphatidylcholine 9 bearing icosadienoyl and docosahexaenoyl groups at the 1-and 2-positions respectively was synthesized. The synthetic route involves carbon chain elongation of linoleic acid via malonic ester synthesis, preparation of lyso-phosphatidylcholine via lipase-catalyzed mono-acylation of 2-O-methoxyethoxymethylglycerol and phosphodiester synthesis, and finally DCC-mediated esterification.
