502-70-5 Usage
Description
(2E,4E,6E,8E,10E,12E,14E)-2,6,11,15-Tetramethyl-2,4,6,8,10,12,14-hexadecaheptenedial is a complex organic compound characterized by its multiple carbon-carbon double bonds (E configuration) and a dialdehyde functional group. It is a tetramethyl-substituted hexadecaheptenedial, which suggests it has a long carbon chain with four methyl groups attached at specific positions along the chain.
Uses
1. Used in Pharmaceutical Industry:
(2E,4E,6E,8E,10E,12E,14E)-2,6,11,15-Tetramethyl-2,4,6,8,10,12,14-hexadecaheptenedial is used as a pharmaceutical compound for its potential therapeutic applications. (2E,4E,6E,8E,10E,12E,14E)-2,6,11,15-Tetramethyl-2,4,6,8,10,12,14-hexadecaheptenedial's unique structure may allow it to interact with biological targets, potentially leading to the development of new drugs for various diseases.
2. Used in Cosmetic Industry:
In the cosmetic industry, (2E,4E,6E,8E,10E,12E,14E)-2,6,11,15-Tetramethyl-2,4,6,8,10,12,14-hexadecaheptenedial may be used as an ingredient in skincare products due to its potential antioxidant or anti-aging properties. (2E,4E,6E,8E,10E,12E,14E)-2,6,11,15-Tetramethyl-2,4,6,8,10,12,14-hexadecaheptenedial's ability to interact with biopolymers and macromolecules could make it a valuable addition to formulations aimed at improving skin health and appearance.
3. Used in Research Applications:
As a complex organic molecule, (2E,4E,6E,8E,10E,12E,14E)-2,6,11,15-Tetramethyl-2,4,6,8,10,12,14-hexadecaheptenedial may be utilized in research settings to study its interactions with various biological systems. This could lead to a better understanding of its potential applications and mechanisms of action in different fields, such as medicine, pharmacology, and biotechnology.
4. Used in Antioxidant Formulations:
Given its structural similarity to known antioxidants like β-carotene, (2E,4E,6E,8E,10E,12E,14E)-2,6,11,15-Tetramethyl-2,4,6,8,10,12,14-hexadecaheptenedial may be used as an antioxidant in various applications, such as in the food industry to extend the shelf life of products or in the pharmaceutical industry to protect against oxidative stress-related diseases.
Please note that the specific applications and uses mentioned above are hypothetical and based on the compound's structural features. Further research and development would be required to validate these potential uses.
Check Digit Verification of cas no
The CAS Registry Mumber 502-70-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,0 and 2 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 502-70:
(5*5)+(4*0)+(3*2)+(2*7)+(1*0)=45
45 % 10 = 5
So 502-70-5 is a valid CAS Registry Number.
InChI:InChI=1/C20H24O2/c1-17(11-7-13-19(3)15-21)9-5-6-10-18(2)12-8-14-20(4)16-22/h5-16H,1-4H3/b6-5+,11-7+,12-8+,17-9+,18-10+,19-13+,20-14+
502-70-5Relevant articles and documents
A Short and Efficient Synthesis of Crocetin-dimethylester and Crocetindial
Frederico, Daniel,Marcos Donate, Paulo,Gomes Constantino, Mauricio,Soares Bronze, Erika,Sairre, Mirela I.
, p. 9126 - 9128 (2003)
In this paper we describe an efficient six-step synthesis of crocetin-dimethylester that could be further reduced to a "four-step" synthesis through the use of in situ procedures. The simplicity of the whole process, the ready availability of starting materials, and the high overall yield render this strategy a very attractive synthesis of this very important compound, which is the key intermediate for the synthesis of several carotenoids and other polyene natural products.
Sulfone-mediated syntheses of crocetin derivatives: Regioselectivity of highly functionalized building blocks
Oh, Eun-Taek,Kim, Young-Hun,Jin, Jingquan,Su, Liang,Seo, Jung-Ah,Koo, Sangho
, p. 4712 - 4717 (2014/06/09)
New C5 sulfone building blocks containing a masked polar end group have been devised for the efficient synthesis of carotenoids with polar termini. Chemoselectivity or the regiochemical issue of the highly functionalized units has been carefully addressed depending on the soft or hard nature of electrophiles. These building blocks have been successfully applied to the syntheses of crocetin derivatives, crocetin dial and the novel crocetin dinitrile.
METHODS FOR SYNTHESIS OF CHIRAL INTERMEDIATES OF CAROTENOIDS, CAROTENOID ANALOGS, AND CAROTENOID DERIVATIVES
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Page/Page column 47, (2010/10/20)
A method used for synthesizing intermediates for use in the synthesis of carotenoids and carotenoid analogs, and/or carotenoid derivatives. In some embodiments, the invention includes methods for synthesizing optically active intermediates useful for the synthesis of optically active carotenoids.
