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About This Item
Linear Formula:
C2H5OC6H3(OCH3)CHO
CAS Number:
Molecular Weight:
180.20
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
204-382-1
MDL number:
Product Name
4-Ethoxy-3-methoxybenzaldehyde, 98%
InChI key
BERFDQAMXIBOHM-UHFFFAOYSA-N
InChI
1S/C10H12O3/c1-3-13-9-5-4-8(7-11)6-10(9)12-2/h4-7H,3H2,1-2H3
SMILES string
CCOc1ccc(C=O)cc1OC
assay
98%
mp
50-53 °C (lit.)
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Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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H Wariishi et al.
The Journal of biological chemistry, 264(24), 14185-14191 (1989-08-25)
In the presence of MnII, H2O2, and glutathione (GSH), manganese peroxidase oxidized veratryl alcohol (I) to veratraldehyde (IV). Anisyl alcohol (II) and benzyl alcohol (III) were also oxidized by this system to their corresponding aldehydes (V and VI). In the
F Cui et al.
Bioorganic & medicinal chemistry, 2(7), 735-742 (1994-07-01)
The degradation of four dimeric lignin model compounds by meso-tetra(2,6-dichloro-3-sulfonatophenyl)porphyrin iron chloride (TDCSPPFeCl) (2) are reported. 4-Ethoxy-3-methoxyphenylglycerol-beta-guaiacyl ether (3) (a beta-0-4 dimer) was cleaved to give 4-ethoxy-3-methoxybenzaldehyde (4) and guaiacol (5) as major products. The oxidation of 1-(4-ethoxy-3-methoxyphenyl)-2-(4-methoxyphenyl)-1,3-propandiol (6, a
Demethylation of Methyl Aryl Ethers: 4-Ethoxy-3-Hydroxybenzaldehyde.
Ireland RE and Walba DM.
Organic Syntheses, 44-44 (1977)
4-Ethoxy-3-methoxybenzaldehyde.
Leka Z, et al.
Acta Crystallographica Section E, Structure Reports Online, 69(12), o1728-o1728 (2013)
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