190849-79-7 Usage
Description
2,4,6,8,10,12,14-Heptadecaheptaen-16-ynal,17-[(4R)-4-hydroxy-2,6,6-trimethyl-1-cyclohexen-1-yl]-2,6,11,15-tetramethyl-,(2E,4E,6E,8E,10E,12E,14E)is a complex polyene compound with a 16-carbon chain and a terminal alkyne functional group. It features a cyclohexenyl group with a hydroxy group at the 4-position, creating a stereogenic center. 2,4,6,8,10,12,14-Heptadecaheptaen-16-ynal,17[(4R)-4-hydroxy-2,6,6-trimethyl-1-cyclohexen1-yl]-2,6,11,15-tetramethyl-,(2E,4E,6E,8E,10E,12E,14E) is highly unsaturated, containing 14 double bonds all in the E configuration. Due to its unique structure and functional groups, it has potential applications in various fields such as organic chemistry, biochemistry, and pharmaceutical research.
Uses
Used in Organic Chemistry:
2,4,6,8,10,12,14-Heptadecaheptaen-16-ynal,17-[(4R)-4-hydroxy-2,6,6-trimethyl-1-cyclohexen-1-yl]-2,6,11,15-tetramethyl-,(2E,4E,6E,8E,10E,12E,14E)is used as a building block for the synthesis of more complex organic molecules. Its multiple double bonds and alkyne functional group allow for various chemical reactions, such as hydrogenation, hydroboration, and cross-coupling, to create new compounds with desired properties.
Used in Biochemistry:
In biochemistry, 2,4,6,8,10,12,14-Heptadecaheptaen-16-ynal,17-[(4R)-4-hydroxy-2,6,6-trimethyl-1-cyclohexen-1-yl]-2,6,11,15-tetramethyl-,(2E,4E,6E,8E,10E,12E,14E)can be employed as a probe to study the interactions between biomolecules and lipids. Its polyene structure and hydroxy group enable it to bind to specific proteins or enzymes, providing insights into their mechanisms of action and potential applications in drug development.
Used in Pharmaceutical Research:
2,4,6,8,10,12,14-Heptadecaheptaen-16-ynal,17-[(4R)-4-hydroxy-2,6,6-trimethyl-1-cyclohexen-1-yl]-2,6,11,15-tetramethyl-,(2E,4E,6E,8E,10E,12E,14E)has potential applications in pharmaceutical research as a lead compound for the development of new drugs. Its unique structure and functional groups can be modified to target specific biological pathways or receptors, potentially leading to the discovery of novel therapeutic agents for various diseases.
Used in the Flavor and Fragrance Industry:
Due to its complex and unique structure, 2,4,6,8,10,12,14-Heptadecaheptaen-16-ynal,17-[(4R)-4-hydroxy-2,6,6-trimethyl-1-cyclohexen-1-yl]-2,6,11,15-tetramethyl-,(2E,4E,6E,8E,10E,12E,14E)may also find applications in the flavor and fragrance industry. Its specific chemical composition could contribute to the creation of new and distinct scents or flavors, enhancing the sensory experience of various products.
Check Digit Verification of cas no
The CAS Registry Mumber 190849-79-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,0,8,4 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 190849-79:
(8*1)+(7*9)+(6*0)+(5*8)+(4*4)+(3*9)+(2*7)+(1*9)=177
177 % 10 = 7
So 190849-79-7 is a valid CAS Registry Number.
190849-79-7Relevant articles and documents
Total synthesis of C31-methyl ketone apocarotenoids 2: The first total synthesis of (3R)-triophaxanthin
Haugan, Jarle Andre
, p. 1096 - 1103 (2007/10/03)
Five possible synthetic strategies have been developed for the synthesis of (all-E)-(3R)-triophaxanthin. A short discussion of these strategies is presented. Fully characterised, optically active (all-E)-(3R)-triophaxanthin was prepared by total synthesis
