59940
Isovanillin
≥95.0%
Sinónimos:
3-Hydroxy-4-methoxybenzaldehyde, 3-Hydroxyanisaldehyde
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About This Item
Fórmula empírica (notación de Hill):
C8H8O3
Número de CAS:
Peso molecular:
152.15
Beilstein/REAXYS Number:
1073021
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
assay
≥95.0%
mp
112-116 °C
functional group
aldehyde
SMILES string
COc1ccc(C=O)cc1O
InChI
1S/C8H8O3/c1-11-8-3-2-6(5-9)4-7(8)10/h2-5,10H,1H3
InChI key
JVTZFYYHCGSXJV-UHFFFAOYSA-N
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Analysis Note
appearance: white/colorless to brown
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
>212.0 °F
flash_point_c
> 100 °C
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Jiyoung Ryu et al.
Archives of pharmacal research, 27(9), 912-914 (2004-10-12)
Seven compounds were isolated from the stem of Acanthopanax senticosus by repeated column chromatography. Their structures were elucidated as isovanillin (1), (-)-sesamin (2), isofraxidin (3), (+)-syringaresinol (4), 5-hydroxymethylfurfural (5), eleutheroside B (6), and eleutheroside E (7) by spectral analysis. Among
Michael D Markey et al.
Organic letters, 9(17), 3255-3257 (2007-07-31)
The first total synthesis of santiagonamine (1) is achieved in 12 steps from isovanillin. A palladium-catalyzed Ullmann cross-coupling reaction and a photocyclization are the key steps in the synthesis.
V Balachandran et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 95, 354-368 (2012-05-01)
This study is a comparative analysis of FT-IR and FT-Raman spectra of vanillin (3-methoxy-4-hydroxybenzaldehyde) and isovanillin (3-hydroxy-4-methoxybenzaldehyde). The molecular structure, vibrational wavenumbers, infrared intensities, Raman scattering activities were calculated for both molecules using the B3LYP density functional theory (DFT) with
Georgios I Panoutsopoulos
Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology, 17(1-2), 47-56 (2006-03-18)
3,4-Dimethoxy-2-phenylethylamine is catalyzed to its aldehyde derivative by monoamine oxidase B, but the subsequent oxidation into the corresponding acid has not yet been studied. Oxidation of aromatic aldehydes is catalyzed mainly by aldehyde dehydrogenase and aldehyde oxidase. The present study
Georgios Panoutsopoulos
Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology, 15(5), 225-232 (2005-06-16)
Homovanillamine is a biogenic amine that it is catalyzed to homovanillyl aldehyde by monoamine oxidase A and B, but the oxidation of its aldehyde to the acid derivative is usually ascribed to aldehyde dehydrogenase and a potential contribution of aldehyde
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