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131119-10-3 | Nonanoic acid, (4-hydroxy-3-methoxyphenyl)methyl ester
CAS No: 131119-10-3 Catalog No: AG000VJ8 MDL No:
Product Description
Catalog Number:
AG000VJ8
Chemical Name:
Nonanoic acid, (4-hydroxy-3-methoxyphenyl)methyl ester
CAS Number:
131119-10-3
Molecular Formula:
C17H26O4
Molecular Weight:
294.3859
IUPAC Name:
(4-hydroxy-3-methoxyphenyl)methyl nonanoate
InChI:
InChI=1S/C17H26O4/c1-3-4-5-6-7-8-9-17(19)21-13-14-10-11-15(18)16(12-14)20-2/h10-12,18H,3-9,13H2,1-2H3
InChI Key:
VSINWHDOHWBJCS-UHFFFAOYSA-N
SMILES:
CCCCCCCCC(=O)OCc1ccc(c(c1)OC)O
Properties
Complexity:
280
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
294.183g/mol
Formal Charge:
0
Heavy Atom Count:
21
Hydrogen Bond Acceptor Count:
4
Hydrogen Bond Donor Count:
1
Isotope Atom Count:
0
Molecular Weight:
294.391g/mol
Monoisotopic Mass:
294.183g/mol
Rotatable Bond Count:
11
Topological Polar Surface Area:
55.8A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
4.8
Literature
| Title | Journal |
|---|---|
| Vanillyl nonanoate protects rat gastric mucosa from ethanol-induced injury through a mechanism involving calcitonin gene-related peptide. | European journal of pharmacology 20110901 |
| Protective effect of capsinoid on lipid peroxidation in rat tissues induced by Fe-NTA. | Free radical research 20051101 |
| Antioxidant activity of capsinoids. | Journal of agricultural and food chemistry 20021204 |
| Enzymatic synthesis of a capsinoid by the acylation of vanillyl alcohol with fatty acid derivatives catalyzed by lipases. | Bioscience, biotechnology, and biochemistry 20020201 |
| Stability of capsinoid in various solvents. | Journal of agricultural and food chemistry 20010801 |
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