127072-60-0 Usage
Description
(2Z,4Z,6Z,8Z)-10-hydroxydodeca-2,4,6,8-tetraenal is a polyunsaturated aldehyde with a long carbon chain and multiple double bonds in a conjugated system. It contains a hydroxy group at the 10th carbon position and is commonly found in some marine organisms. (2Z,4Z,6Z,8Z)-10-hydroxydodeca-2,4,6,8-tetraenal plays a role in chemical signaling and defense mechanisms, making it a potential candidate for use in organic synthesis and bioactive compound studies.
Uses
Used in Organic Synthesis:
(2Z,4Z,6Z,8Z)-10-hydroxydodeca-2,4,6,8-tetraenal is used as a building block in organic synthesis for the creation of various complex organic molecules. Its unique structure with multiple double bonds and a hydroxy group allows for versatile chemical reactions and the formation of diverse products.
Used in Bioactive Compound Studies:
(2Z,4Z,6Z,8Z)-10-hydroxydodeca-2,4,6,8-tetraenal is used as a bioactive compound in research for its potential biological activities. Its presence in marine organisms and role in chemical signaling and defense mechanisms make it an interesting subject for studying its effects on various biological systems and potential applications in medicine or other fields.
Used in Chemical Signaling and Defense Mechanisms Research:
(2Z,4Z,6Z,8Z)-10-hydroxydodeca-2,4,6,8-tetraenal is used as a model compound in research to understand the role of chemical signaling and defense mechanisms in marine organisms. Its unique structure and properties can provide insights into the development of new strategies for chemical communication and protection against predators or other threats.
Check Digit Verification of cas no
The CAS Registry Mumber 127072-60-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,0,7 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 127072-60:
(8*1)+(7*2)+(6*7)+(5*0)+(4*7)+(3*2)+(2*6)+(1*0)=110
110 % 10 = 0
So 127072-60-0 is a valid CAS Registry Number.
127072-60-0Relevant articles and documents
Acid-catalyzed solvolysis of polyenol ethers. III. Effect of the alkoxy moiety
Nieuwenhuis, Saskia A. M.,Vertegaal, Louis B. J.,De Zoete, Marian C.,Van Der Gen, Arne
, p. 13207 - 13230 (2007/10/02)
The dependence of the solvolysis of polyenol ethers on the nature of the alkoxy moiety has been studied. A new reaction path, leading to the formation of ω-hydroxy (methoxy) substituted aldehydes and -esters, was established. The proposed reaction pathway (scheme 6) is initiated by an electron transfer from the polyenol ether to molecular oxygen, followed by combination of the two radicals to a peroxide zwitterion. Upon protonation, solvent adds to the ω-carbon atom of the polyene to give an intermediate that can either loose water to form an ester, or loose the alkoxy moiety to give an aldehyde. This mechanism is believed to be involved in the strong mutagenic activity displayed by many polyenol ethers, including the natural mutagen fecapentaene-12.
