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Merck

07-4260

Sigma-Aldrich

N,N-Dimethylanilin

SAJ first grade, ≥99.0%

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About This Item

Lineare Formel:
C6H5N(CH3)2
CAS-Nummer:
Molekulargewicht:
121.18
Beilstein:
507140
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:

Qualität

SAJ first grade

Assay

≥99.0%

Form

liquid

Verfügbarkeit

available only in Japan

Brechungsindex

n20/D 1.557 (lit.)

pH-Wert

7.4 (20 °C, 1.2 g/L)

bp

193-194 °C (lit.)

mp (Schmelzpunkt)

1.5-2.5 °C (lit.)

Dichte

0.956 g/mL at 25 °C (lit.)

SMILES String

CN(C)c1ccccc1

InChI

1S/C8H11N/c1-9(2)8-6-4-3-5-7-8/h3-7H,1-2H3

InChIKey

JLTDJTHDQAWBAV-UHFFFAOYSA-N

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Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 2 - Carc. 2

Lagerklassenschlüssel

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flammpunkt (°F)

143.6 °F

Flammpunkt (°C)

62 °C


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Marius Koch et al.
Journal of the American Chemical Society, 134(8), 3729-3736 (2012-01-31)
The fluorescence quenching of 3-cyanoperylene upon electron transfer from N,N-dimethylaniline in three room-temperature ionic liquids (RTILs) and in binary solvent mixtures of identical viscosity has been investigated using steady-state and time-resolved fluorescence spectroscopy. This study was stimulated by previous reports
Cai-Rong Zhang et al.
Journal of molecular graphics & modelling, 38, 419-429 (2012-11-03)
The photon to current conversion efficiency of dye-sensitized solar cells (DSCs) can be significantly affected by dye sensitizers. The design of novel dye sensitizers with good performance in DSCs depend on the dye's information about electronic structures and optical properties.
Kefeng Liu et al.
Dalton transactions (Cambridge, England : 2003), 41(12), 3461-3467 (2012-02-04)
A number of new half-sandwich zirconium(IV) complexes bearing N,N-dimethylaniline-amido ligands with the general formula Cp*ZrCl(2)[ortho-(RNCH(2))(Me(2)N)C(6)H(4)] [R = 2,6-Me(2)C(6)H(3) (1), 2,6-(i)Pr(2)C(6)H(3) (2), (i)Pr (3), (t)Bu (4)] were synthesized by the reaction of Cp*ZrCl(3) with the corresponding ortho-(Me(2)N)C(6)H(4)CH(2)NRLi. All new zirconium complexes
Yong Wang et al.
The journal of physical chemistry. B, 114(8), 2964-2970 (2010-02-12)
This paper addresses the experimentally observed mechanistic differences between the cytochrome P450-catalyzed N-demethylation of substituted N,N-dimethylanilines (DMA) and of N,N-dimethylbenzamides (DMBA). The two reactions of these substrates are initiated by C-H activation of the methyl groups on the nitrogen. Thus
Subashani Maniam et al.
Organic letters, 10(10), 1885-1888 (2008-04-16)
Cyclodextrin [2]rotaxanes have been prepared by coupling dimethylanilines with dicarboxylic acids using DMT-MM, in aqueous solutions of alpha-cyclodextrin, and the example illustrated shows unusual fluorescence emission and other spectroscopic behavior characteristic of the formation of molecular wires in solution, similar

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