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Sigma-Aldrich

2,4-Dimethylanisole

97%

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About This Item

Linear Formula:
(CH3)2C6H3OCH3
CAS Number:
6738-23-4
Molecular Weight:
136.19
EC Number:
229-794-9
MDL number:
MFCD00008377
UNSPSC Code:
12352100
PubChem Substance ID:
24848329

assay

97%

refractive index

n20/D 1.514 (lit.)

bp

191 °C (lit.)

density

0.973 g/mL at 25 °C (lit.)

SMILES string

COc1ccc(C)cc1C

InChI

1S/C9H12O/c1-7-4-5-9(10-3)8(2)6-7/h4-6H,1-3H3

InChI key

UJCFZCTTZWHRNL-UHFFFAOYSA-N

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Application

2,4-Dimethylanisole was used to study the solvolysis of 1,4-dimethyl-4-nitrocyclohexa-2,5-dien-1. It was used to study the photolysis of charge transfer complex of 2,4-dimethylanisole with tetranitromethane.

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Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

145.4 °F - closed cup

flash_point_c

63 °C - closed cup

Certificates of Analysis (COA)

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Photochemical Nitration by Tetranitromethane. Part XXXVII. t Adduct Formation and the Regiochemistry of Attack of Trinitromethanide Ion on Radical Cations in the Photochemical Reactions of 2-Methyl-, 2, 3-Dimethyl-and 2, 4-Dimethylanisoles.
Timmerman-Vaughan DJ.
Acta Chemica Scandinavica, 51(19971), 73-87 (1997)
The role of ion-molecule pair intermediates in acid-catalyzed solvolysis. General base-catalyzed formation of 4-methylbenzyl carbocation and its trapping by nucleophiles.
Thibblin A.
The Journal of Organic Chemistry, 58(26), 7427-7433 (1993)
Reactions of the 1-hydroxy-1, 4-dimethylcyclohexadienyl cation, an intermediate in the solvolysis of 1, 4-dimethyl-4-nitrocyclohexa-2, 5-dien-1-ol.
Fischer A, et al.
Canadian Journal of Chemistry, 64(6), 1093-1101 (1986)

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