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137480

Sigma-Aldrich

2,5-Dimethylanisole

99%

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About This Item

Linear Formula:
(CH3)2C6H3OCH3
CAS Number:
1706-11-2
Molecular Weight:
136.19
EC Number:
216-943-8
MDL number:
MFCD00008378
UNSPSC Code:
12352100
PubChem Substance ID:
24848330
NACRES:
NA.22

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

Related Categories

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 Code

10 - Combustible liquids

WGK

WGK 3

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

137480-100G:
137480-VAR:
137480-25G:
137480-BULK:

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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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