Interesting facts
Intriguing Insights into the Compound
This fascinating compound, known for its complex structure and unique properties, is a prime example of the intricate combinations found within organic chemistry. Here are some intriguing facts about it:
- Synthetic Origin: The compound belongs to a class of organic molecules that are often synthesized for use in various applications, particularly in biochemistry and materials science.
- Biological Relevance: Members of this compound family are frequently explored for their potential biological activities, especially in the field of pharmacology, where they may exhibit antioxidant properties.
- Role of Chroman: The chroman moiety, central to the structure, is important in nature as it can enhance the stability and bioactivity of compounds in pharmaceutical development.
- Stereochemistry Matters: With its multiple chiral centers, this compound showcases the significance of stereochemistry in determining the properties and behaviors of molecules, influencing how they interact with biological systems.
- Applications in Research: Researchers are investigating this compound for its potential applications in the development of new drugs and materials, highlighting its importance in the advancement of medicinal chemistry.
- Structure-Activity Relationship: Studies often focus on understanding how modifications in the structure of such compounds influence their activity, guiding chemists in synthesis and optimization efforts.
As you delve deeper into this compound, remember that the world of chemistry is a realm of infinite possibilities, where every structure holds a potential story waiting to be explored. Embrace the complexity and the beauty of the molecular architecture!
Synonyms
Vitamin E Nicotinate
43119-47-7
Renascin
TOCOPHERYL NICOTINATE
Vitamin E nicotinic acid ester
WI1J5UCY5C
[(2R)-2,5,7,8-tetramethyl-2-[(4R,8R)-4,8,12-trimethyltridecyl]chroman-6-yl] pyridine-3-carboxylate
((2R)-2,5,7,8-tetramethyl-2-((4R,8R)-4,8,12-trimethyltridecyl)chroman-6-yl) pyridine-3-carboxylate
Tocoferil nicotinate
tocopherol nicotinate
51898-34-1
16676-75-8
(R)-2,5,7,8-Tetramethyl-2-((4R,8R)-4,8,12-trimethyltridecyl)chroman-6-yl nicotinate
DL-alpha tocopheryl nicotinate
(+/-)-alpha-Tocopherol nicotinate
dl-alpha-Tocopherol nicotinate
DL-alpha-Tocopheryl Nicotinate
( inverted exclamation markA)-|A-Tocopherol nicotinate
MFCD03548047
Tocopherol nicotinate [JAN]
D-alpha tocopheryl nicotinate
QCP2FMP7I8
Alpha-tocopheryl nicotinate
C35H53NO3
[(2R)-2,5,7,8-tetramethyl-2-[(4R,8R)-4,8,12-trimethyltridecyl]-3,4-dihydrochromen-6-yl] pyridine-3-carboxylate
3-Pyridinecarboxylic acid, (2R)-3,4-dihydro-2,5,7,8-tetramethyl-2-[(4R,8R)-4,8,12-trimethyltridecyl]-2H-1-benzopyran-6-yl ester
CHEMBL1084541
DTXSID1046396
CHEBI:32239
(2R-(2R*(4R*,8R*)))-3,4-Dihydro-2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)-2H-1-benzopyran-6-yl nicotinate
NCGC00164499-01
NCGC00164499-03
rel-(R)-2,5,7,8-Tetramethyl-2-((4R,8R)-4,8,12-trimethyltridecyl)chroman-6-yl nicotinate
DTXCID9026396
Juvela nicotinate
Kentons
3-Pyridinecarboxylic acid, (2R)-3,4-dihydro-2,5,7,8-tetramethyl-2-((4R,8R)-4,8,12-trimethyltridecyl)-2H-1-benzopyran-6-yl ester
CAS-43119-47-7
EINECS 256-101-7
UNII-QCP2FMP7I8
UNII-WI1J5UCY5C
Alpha-Tocophenyl nicotinate
BRN 0466142
alpha-Tocopherol nicotinate, DL-
(R)-2,5,7,8-Tetramethyl-2-[(4R,8R)-4,8,12-trimethyltridecyl]chroman-6-yl Nicotinate
(2R)-2-((4R,8R)-4,8,12-trimethyltridecyl)-2,5,7,8-tetramethylchroman-6-yl pyri dine-3-carboxylate
3-Pyridinecarboxylic acid, 3,4-dihydro-2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)-2H-1-benzopyran-6-yl ester, (2R-(2R*(4R*,8R*)))-
D-ALPHA-TOCOPHERYL NICOTINATE
EINECS 257-501-4
Juvela nicotinate (TN)
alpha-toco-pherol nicotinate
SCHEMBL42668
Tocopherol nicotinate (JP18)
orb1705644
SCHEMBL29356548
HY-B0757A
DTXSID401019802
HY-B0757
Tox21_112137
BDBM50318914
SBB058193
TOCOFERIL NICOTINATE [MART.]
(+/-)- alpha -Tocopherol nicotinate
AKOS015896058
TOCOPHERYL NICOTINATE [WHO-DD]
Tox21_112137_1
AC-6859
DL-.ALPHA.-TOCOPHERYL NICOTINATE
NCGC00164499-02
TOCOPHERYL NICOTINATE, D-.ALPHA.
(2R*(4R*,8R*))-(1)-3,4-Dihydro-2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)-2H-1-benzopyran-6-yl nicotinate
(2R-(2R*(4R*,8R*)))-3-Pyridinecarboxylic acid, 3,4-dihydro-2,5,7,8tetramethyl-2-(4,8,12-trimethyltridecyl)-2H-1-benzopyran-6-yl ester
3-Pyridinecarboxylic acid, 3,4-dihydro-2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)-2H-1- -benzopyran-6-yl ester
AS-15224
SY428076
.ALPHA.-TOCOPHEROL NICOTINATE, D-
.ALPHA.-TOCOPHEROL NICOTINATE, DL-
J299.341D
TOCOPHERYL NICOTINATE, DL-.ALPHA.-
CS-0144088
NS00020307
ST51015145
D01530
E80396
DL-.ALPHA.-TOCOPHEROL NICOTINIC ACID ESTER
SR-01000944628
SR-01000944628-2
Q27114834
3-PYRIDINECARBOXYLIC ACID, 3,4-DIHYDRO-2,5,7,8-TETRAMETHYL-2-(4,8,12-TRIMETHYLTRIDECYL)-2H-1-BENZOPYRAN-6-YL ESTER, (2R*(4R*,8R*))-(+/-)-
Solubility of [(2R)-2,5,7,8-tetramethyl-2-[(4R,8R)-4,8,12-trimethyltridecyl]chroman-6-yl] pyridine-3-carboxylate
The solubility of this complex compound primarily depends on its structure and functional groups. Substances with multiple alkyl groups and polar functional groups often exhibit diverse solubility characteristics. Here are some key points regarding the solubility of this compound:
In conclusion, while this compound's intricate structure suggests a complex solubility profile, the overall solubility can be summarized as predominantly influenced by its polar and non-polar features. Thus, one might anticipate limited aqueous solubility and more favorable solubility in organic mediums.