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163252

Sigma-Aldrich

3,4-Dimethoxytoluene

96%

Sinónimos:

4-Methylveratrole

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About This Item

Fórmula lineal:
CH3C6H3(OCH3)2
Número de CAS:
494-99-5
Peso molecular:
152.19
Beilstein/REAXYS Number:
2045328
EC Number:
207-796-0
MDL number:
MFCD00016651
UNSPSC Code:
12352100
PubChem Substance ID:
24850032

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.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

183.2 °F - closed cup

flash_point_c

84 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
MKBC9257V
MKBC9257
MKBC8215
MKBC0776
MKBC0285

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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.
Bernini R, et al.
Tetrahedron, 62(33), 7733-7737 (2006)
Dimitris S Argyropoulos et al.
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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Acta tropica, 128(3), 557-560 (2013-08-21)
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
Evon Powell et al.
International journal of nanomedicine, 2(3), 449-459 (2007-11-21)
The interaction of the important but often overdosed local anesthetic bupivacaine, its structural analogs 2,6-dimethylaniline, and N-methyl-2,6-dimethylacetanilide, and cocaine, with several electron deficient aromatic moieties were studied primarily by proton NMR and UV-visible spectroscopy. In solution, the anesthetic, its analogs
D K Joshi et al.
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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