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(2E,4E,6E,8E,10E,12E)-2,7,11-trimethyl-13-(2,6,6-trimethylcyclohex-1-en-1-yl)trideca-2,4,6,8,10,12-hexaene-1-ol is a complex organic compound characterized by its long carbon chain and multiple double bonds. It features a trideca-hexaene backbone with six conjugated double bonds, which are essential for its unique electronic structure and potential applications in various chemical reactions. The compound also contains three methyl groups at the 2, 7, and 11 positions, and a cyclohex-1-en-1-yl group at the 13th position, which adds to its structural complexity. This molecule is a prime example of the diversity and intricacy found in organic chemistry, with potential applications in the synthesis of natural products and pharmaceuticals.

1050-75-5

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1050-75-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1050-75-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,5 and 0 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1050-75:
(6*1)+(5*0)+(4*5)+(3*0)+(2*7)+(1*5)=45
45 % 10 = 5
So 1050-75-5 is a valid CAS Registry Number.

1050-75-5Relevant academic research and scientific papers

Synthesis of apocarotenoids by acyclic cross metathesis and characterization as substrates for human retinaldehyde dehydrogenases

Domínguez, Marta,Pequerul, Raquel,Alvarez, Rosana,Giménez-Dejoz, Joan,Birta, Eszter,Porté, Sergio,Rühl, Ralph,Parés, Xavier,Farrés, Jaume,de Lera, Angel R.

, p. 2567 - 2574 (2018/04/19)

A new synthesis of three apocarotenoids, namely 14′-apo-β-carotenal, 12′-apo-β-carotenal and 10′-apo-β-carotenal, has been achieved that is based on the acyclic cross-metathesis of the hexaene derived from retinal and the corresponding partners. These compounds can be enzymatically converted to their carboxylic acids by the human aldehyde dehydrogenases involved in retinaldehyde oxidation. Their kinetic parameters suggest that these enzymes might play a role in the physiological metabolism of apocarotenoids.

Total Synthesis of Acetylenic Carotenoids. 2. Synthesis of (all-E)-(3R,3'R)-Diatoxanthin and (all-E)-(3R)-7,8-Didehydrocryptoxanthin

Haugan, Jarle Andre,Liaaen-Jensen, Synnoeve

, p. 899 - 904 (2007/10/02)

Optically active (all-E)-(3R,3'R)-diatoxanthin, indistinguishable from the natural carotenol, has been prepared by total synthesis for the first time with 34percent overall yield in four steps from the available (2E)-5-(4R)-4-hydroxy-2,6,6-trimethylcyclo

Electronic Relaxation in Long Polyenes

Cosgrove, Sarah A.,Guite, Melissa A.,Burnell, Timothy B.,Christensen, Ronald L.

, p. 8118 - 8124 (2007/10/02)

A series of carotenols with from 7 to 11 conjugated double bonds have been synthesized and purified using HPLC techniques.Absorption, fluorescence, and fluorescence excitation spectra have been obtained in 77 K glasses.The shorter members of this series e

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