55303-96-3 Usage
Description
Dodeca-4,8-dienedial, with the molecular formula C12H18O2, is an unsaturated aldehyde featuring a 12-carbon chain with a diene functional group and a carbonyl group. This highly reactive compound is known for its potential applications in various fields, including organic synthesis and the development of anti-cancer properties.
Uses
Used in Organic Synthesis:
Dodeca-4,8-dienedial is utilized as a reagent in organic synthesis for its high reactivity, enabling the creation of various complex organic compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, dodeca-4,8-dienedial is studied for its potential anti-cancer properties, as it has been found to inhibit the growth of certain cancer cell lines.
Used in Fragrance and Flavor Production:
Dodeca-4,8-dienedial is employed as a building block in the production of fragrances and flavors, contributing to the development of unique scents and tastes.
Used in Polymer Manufacturing:
dodeca-4,8-dienedial is also used in the manufacturing of polymers, where its reactive nature aids in the formation of diverse polymeric materials for various applications.
Used in Industrial Applications:
Beyond the aforementioned uses, dodeca-4,8-dienedial finds its place in other industrial applications, capitalizing on its reactivity and functional groups.
However, due to its potential for irritation and toxicity, dodeca-4,8-dienedial should be handled with care to ensure safety in all applications.
Check Digit Verification of cas no
The CAS Registry Mumber 55303-96-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,3,0 and 3 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 55303-96:
(7*5)+(6*5)+(5*3)+(4*0)+(3*3)+(2*9)+(1*6)=113
113 % 10 = 3
So 55303-96-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H18O2/c13-11-9-7-5-3-1-2-4-6-8-10-12-14/h3-6,11-12H,1-2,7-10H2
55303-96-3Relevant articles and documents
Polyether Natural Product Inspired Cascade Cyclizations: Autocatalysis on π-Acidic Aromatic Surfaces
Hao, Xiaoyu,Matile, Stefan,Paraja, Miguel
, p. 15093 - 15097 (2020)
Anion-π catalysis functions by stabilizing anionic transition states on aromatic π surfaces, thus providing a new approach to molecular transformation. The delocalized nature of anion–π interactions suggests that they serve best in stabilizing long-distance charge displacements. Aiming therefore for an anionic cascade reaction that is as charismatic as the steroid cyclization is for conventional cation-π biocatalysis, reported here is the anion-π-catalyzed epoxide-opening ether cyclizations of oligomers. Only on π-acidic aromatic surfaces having a positive quadrupole moment, such as hexafluorobenzene to naphthalenediimides, do these polyether cascade cyclizations proceed with exceptionally high autocatalysis (rate enhancements kauto/kcat >104 m?1). This distinctive characteristic adds complexity to reaction mechanisms (Goldilocks-type substrate concentration dependence, entropy-centered substrate destabilization) and opens intriguing perspectives for future developments.
