163252
3,4-Dimethoxytoluene
96%
Synonym(s):
4-Methylveratrole
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About This Item
Linear Formula:
CH3C6H3(OCH3)2
CAS Number:
Molecular Weight:
152.19
Beilstein:
2045328
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
Assay
96%
refractive index
n20/D 1.528 (lit.)
bp
133-135 °C/50 mmHg (lit.)
mp
22-23 °C (lit.)
density
1.051 g/mL at 25 °C (lit.)
SMILES string
COc1ccc(C)cc1OC
InChI
1S/C9H12O2/c1-7-4-5-8(10-2)9(6-7)11-3/h4-6H,1-3H3
InChI key
GYPMBQZAVBFUIZ-UHFFFAOYSA-N
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General description
3,4-Dimethoxytoluene is the main component of essential oil isolated from Phoenix dactylifera L. It was selectively oxidized to the corresponding 1,4-benzoquinones in the presence of hydrogen peroxide/methyltrioxorhenium in 1-butyl-3-methylimidazolium tetrafluoroborate.
Application
3,4-Dimethoxytoluene was used as an internal standard in HPLC quantifications.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
183.2 °F - closed cup
Flash Point(C)
84 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Convenient oxidation of alkylated phenols and methoxytoluenes to antifungal 1, 4-benzoquinones with hydrogen peroxide (H2O2)/methyltrioxorhenium (CH3 ReO3) catalytic system in neutral ionic liquid.
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Journal of agricultural and food chemistry, 50(4), 658-666 (2002-02-07)
To define the abundance and comprehend the reactivity of dibenzodioxocins in lignin, model compound studies, specific degradation experiments on milled wood lignin, and molecular modeling calculations have been performed. Quantitative (31)P NMR measurements of the increase of biphenolic hydroxyl groups
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Date palm, Phoenix dactylifera L. (Arecaceae), grows commonly in the Arabian Peninsula and is traditionally used to treat various diseases. The aim of the present study was to identify chemical composition of the essential oil and to investigate the repellent
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European journal of biochemistry, 237(1), 45-57 (1996-04-01)
The stabilities of the cation radicals of veratryl alcohol, 3,4-dimethoxytoluene and 1,4-dimethoxybenzene were compared by monitoring the formation of dimeric products during the oxidation of these substrates by lignin peroxidase (LiP). LiP oxidized veratryl alcohol to generate veratraldehyde as the
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