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137499

Sigma-Aldrich

3,4-Dimethylanisole

99%

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About This Item

Linear Formula:
(CH3)2C6H3OCH3
CAS Number:
4685-47-6
Molecular Weight:
136.19
EC Number:
225-142-2
MDL number:
MFCD00008396
UNSPSC Code:
12352100
PubChem Substance ID:
24848331
NACRES:
NA.22

Quality Level

100

assay

99%

form

liquid

refractive index

n20/D 1.517 (lit.)

bp

200-201 °C (lit.)

density

0.974 g/mL at 25 °C (lit.)

SMILES string

COc1ccc(C)c(C)c1

InChI

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

InChI key

LVUBSVWMOWKPDJ-UHFFFAOYSA-N

Application

3,4-Dimethylanisole was used as starting reagent in the synthesis of 3- and 4-methoxy-N-hydroxyphthalimide.

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

168.8 °F - closed cup

flash_point_c

76 °C - closed cup

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Certificates of Analysis (COA)

Lot/Batch Number
MKBT6860V
MKBQ5236V
SHBC1037V
MKBH8036V
MKBH0025V

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N-Hydroxyphthalimide/Cobalt (II) Catalyzed Low Temperature Benzylic Oxidation Using Molecular Oxygen.
Wentzel BB, et al.
Tetrahedron, 56(39), 7797-7803 (2000)
Kamila K Mentel et al.
Nature communications, 9(1), 2903-2903 (2018-07-27)
Electron transfer reactions are arguably the simplest chemical reactions but they have not yet ceased to intrigue chemists. Charge-separation and charge-recombination reactions are at the core of life-sustaining processes, molecular electronics and solar cells. Intramolecular electron donor-acceptor systems capture the

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