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D139505

Sigma-Aldrich

4-(Dimethylamino)benzonitrile

98%

Sinónimos:

4-Cyano-N,N-dimethylaniline, DMABN

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About This Item

Fórmula lineal:
(CH3)2NC6H4CN
Número de CAS:
1197-19-9
Peso molecular:
146.19
Beilstein/REAXYS Number:
971606
EC Number:
214-819-8
MDL number:
MFCD00001815
UNSPSC Code:
12352100
PubChem Substance ID:
24893427
NACRES:
NA.22

assay

98%

form

crystals

bp

318 °C (lit.)

mp

72-75 °C (lit.)

SMILES string

CN(C)c1ccc(cc1)C#N

InChI

1S/C9H10N2/c1-11(2)9-5-3-8(7-10)4-6-9/h3-6H,1-2H3

InChI key

JYMNQRQQBJIMCV-UHFFFAOYSA-N

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Categorías relacionadas

General description

4-(Dimethylamino)benzonitrile is extensively used in photophysical studies due to its ability to undergo intramolecular charge transfer (ICT) from the dimethylamino moiety to the cyanophenyl moiety on photo-excitation leading to the appearance of dual fluorescence.

Application

4-(Dimethylamino)benzonitrile can be used in the synthesis of 3,6-diphenyl-2,5-dihydro-pyrrolo[3,4-c]pyrrole-1,4-dione derivatives.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

Certificados de análisis (COA)

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Sigma-Aldrich

B58407

4-Bromobenzonitrile

4-(Dimethylamino)benzaldehyde ACS reagent, 99%

Sigma-Aldrich

156477

4-(Dimethylamino)benzaldehyde

Victor A Galievsky et al.
The journal of physical chemistry. A, 115(40), 10823-10845 (2011-08-02)
The excited state behavior of the six m,n-dicyano-N,N-dimethylanilines (mnDCDMA) and m,n-dicyano-(N-methyl-N-isopropyl)anilines (mnDCMIA) is discussed as a function of solvent polarity and temperature. The dicyano moiety in these electron donor (D)/acceptor (A) molecules has a considerably larger electron affinity than the
Comparative chemical mutagenesis; well designed and well assessed. Comparative genetic toxicology: the second UK EMS Collaborative Study.
F H Sobels
Mutation research, 157(2-3), 107-110 (1985-08-01)
Rômulo A Ando et al.
Physical chemistry chemical physics : PCCP, 19(36), 25151-25157 (2017-09-09)
In this work we demonstrate the use of the push-pull model system 4-(dimethylamino)benzonitrile (DMABN) as a convenient molecular probe to investigate the local solvation structure and dynamics by means of time-resolved infrared spectroscopy (TRIR). The photochemical features associated with this
Mohammed H Ahmed et al.
The journal of adhesive dentistry, 21(2), 117-132 (2019-04-06)
Universal adhesives use a combined primer/bonding resin applied either in 2-step etch-and-rinse (2-E&R) or 1-step self-etch (1-SE) mode. This study investigated whether three universal adhesives would benefit from an extra bonding layer (EBL), essentially making them 3-step E&R (3-E&R) and
The formation of a novel mercapturic acid during the metabolism of an N-methyl aromatic amine, 4-cyano-N,N-dimethylaniline.
C J Logan et al.
Biochemical pharmacology, 33(14), 2345-2346 (1984-07-15)
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