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Merck
CN

516406

4-Ethoxy-3-methoxybenzaldehyde

98%

Synonym(s):

4-Ethoxy-m-anisaldehyde

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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:
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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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