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2,4,6,8,10,12,14,16-Heptadecaoctaenoic acid, 2,6,11,15-tetramethyl-17-(2,6,6-trimethyl-1-cyclohexen-1-yl)-, (2E,4E,6E,8E,10E,12E,14E,16E)- is a complex organic compound with a long chain of 17 carbon atoms, featuring eight double bonds (denoted by the E configuration, indicating the trans arrangement of the double bonds). The molecule also contains four methyl groups at positions 2, 6, 11, and 15, and a unique cyclohexenyl group at position 17, which is itself substituted with three methyl groups. 2,4,6,8,10,12,14,16-Heptadecaoctaenoicacid, 2,6,11,15-tetramethyl-17-(2,6,6-trimethyl-1-cyclohexen-1-yl)-,(2E,4E,6E,8E,10E,12E,14E,16E)- is characterized by its highly unsaturated nature, which is typical for polyenoic fatty acids, and its specific structural features may influence its chemical properties and potential applications in various fields, such as pharmaceuticals or materials science.

1962-15-8

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1962-15-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1962-15-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,6 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1962-15:
(6*1)+(5*9)+(4*6)+(3*2)+(2*1)+(1*5)=88
88 % 10 = 8
So 1962-15-8 is a valid CAS Registry Number.

1962-15-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2E,4E,6Z,8E,10E,12E,14E,16E)-2,6,11,15-tetramethyl-17-(2,6,6-trimethylcyclohexen-1-yl)heptadeca-2,4,6,8,10,12,14,16-octaenoic acid

1.2 Other means of identification

Product number -
Other names Apo-8'-carotenoic Acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1962-15-8 SDS

1962-15-8Relevant academic research and scientific papers

Light harvesting and photoprotective functions of carotenoids in compact artificial photosynthetic antenna designs

Kodis, Gerdenis,Herrero, Christian,Palacios, Rodrigo,Marinì?o-Ochoa, Ernesto,Gould, Stephanie,De La Garza, Linda,Van Grondelle, Rienk,Gust, Devens,Moore, Thomas A.,Moore, Ana L.,Kennis, John T.M.

, p. 414 - 425 (2007/10/03)

Artificial light-harvesting constructs were synthesized by covalently linking two carotenoids to the central silicon atom of a phthalocyanine (Pc) derivative. Triad 1 binds two carotenoids having nine conjugated double bonds, whereas triad 2 binds two carotenoids having 10 carbon-carbon double bonds in conjugation. Fluorescence excitation experiments indicated that, in triad 1 dissolved in n-hexane, the carotenoid to Pc singlet energy transfer efficiency is ca. 92%, whereas in triad 2, it is 30%. Results from ultrafast laser spectroscopy indicate that upon population of the optically allowed S2 state of the carotenoid the optically forbidden states S1 and S* are rapidly generated in both triad 1 and triad 2. In triad 1, S2, S1 and S* all contribute singlet electronic energy to Pc. In triad 2, singlet electronic energy transfer to Pc occurs primarily from the optically allowed S2 state with little energy transfer to Pc via the S1 state, and there is no evidence for energy transfer via S*. Instead, in triad 2, we find a multiphased quenching of the Pc singlet excited state on the picosecond and nanosecond time scales. Upon intersystem crossing from the singlet excited state of Pc to the triplet state in triad 1, triplet-triplet energy transfer to either of the carotenoids takes place on a time scale significantly shorter than 5 ns. When dissolved in polar solvents, triads 1 and 2 exhibit light-induced electron transfer from either of the carotenoid moieties to the excited singlet Pc species with a time constant of about 2 ps. Charge recombination to the singlet ground state occurs in 10 ps in triad 1 and 17 ps in triad 2.

Combination of vitamin E with a carotenoid: α-tocopherol and trolox linked to β-apo-8'-carotenoic acid

Larsen, Eva,Abendroth, Jan,Partali, Vassilia,Schulz, Bernhard,Sliwka, Hans-Richard,Quartey, Edward G. K.

, p. 113 - 117 (2007/10/03)

Vitamin E and carotenoids show many similar and complementary properties and protect living tissues against a variety of pathological processes. A mixture of both compounds often exhibits a significantly greater effect than the sum of the individual activ

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