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137480

Sigma-Aldrich

2,5-Dimethylanisole

99%

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Linear Formula:
(CH3)2C6H3OCH3
CAS Number:
Molecular Weight:
136.19
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

99%

form

liquid

refractive index

n20/D 1.514 (lit.)

bp

190 °C (lit.)

density

0.965 g/mL at 25 °C (lit.)

SMILES string

COc1cc(C)ccc1C

InChI

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

InChI key

SJZAUIVYZWPNAS-UHFFFAOYSA-N

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D146404D146609137499
vibrant-m

137480

2,5-Dimethylanisole

vibrant-m

D146404

2,6-Dimethylanisole

vibrant-m

D146609

3,5-Dimethylanisole

vibrant-m

137499

3,4-Dimethylanisole

Quality Level

100

Quality Level

200

Quality Level

100

Quality Level

100

density

0.965 g/mL at 25 °C (lit.)

density

0.962 g/mL at 25 °C (lit.)

density

0.963 g/mL at 25 °C (lit.)

density

0.974 g/mL at 25 °C (lit.)

bp

190 °C (lit.)

bp

182 °C (lit.)

bp

193 °C (lit.)

bp

200-201 °C (lit.)

refractive index

n20/D 1.514 (lit.)

refractive index

n20/D 1.503 (lit.)

refractive index

n20/D 1.512 (lit.)

refractive index

n20/D 1.517 (lit.)

form

liquid

form

liquid

form

liquid

form

liquid

General description

2,5-Dimethylanisole acts as photoexcited donor and undergoes different non-radiative transitions in the presence of the acceptor 2-nitrofluorene in ethanol rigid glassy matrix at 77K.

Application

2,5-Dimethylanisole was used to investigate the temperature dependence of spin-rotational relaxation rate of methyl C-13 in 2, 5-dimethylaniline.

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3


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Investigations on the nature of non-radiative transitions from excited singlet and triplet states of dimethyl substituted phenols in the presence of acceptor 2-nitrofluorene at 77K.
Sinha S and Ganguly T.
Journal of Photochemistry and Photobiology A: Chemistry, 117(2), 83-90 (1998)
C13 NMR Relaxation study of Internal Rotation of Methyl Groups-Spin-Rotational Relaxation of Methyl Carbon-13 in 2-bromo-p-xylene, 2, 5-dimethylanisole and 2, 5-dimethylaniline.
Lee JW, et al.
Bull. Korean Chem. Soc., 8(2), 73-79 (1987)
Ya-Nan Zhang et al.
Journal of hazardous materials, 358, 216-221 (2018-07-11)
Pharmaceuticals are a group of ubiquitous emerging pollutants, many of which have been shown to undergo efficient photolysis in the environment. Photochemically produced reactive intermediates (PPRIs) sensitized by the pharmaceuticals in sunlit natural waters may induce photodegradation of coexisting compounds.
Manabu Nakazono et al.
Clinica chimica acta; international journal of clinical chemistry, 436, 27-34 (2014-05-13)
Various styrylbenzene compounds were synthesized and evaluated as mainly Aβ amyloid sensors. These compounds, however, cannot be used for detecting amyloid deposition in peripheral nerves because of the inherent sensitivity of the compounds. These compounds often generate false positives especially

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