109762
4-(Dimethylamino)benzaldehyde
98%
Synonyme(s) :
Ehrlich’s reagent
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A propos de cet article
Formule linéaire :
(CH3)2NC6H4CHO
Numéro CAS:
Poids moléculaire :
149.19
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-819-0
Beilstein/REAXYS Number:
606802
MDL number:
Assay:
98%
Form:
solid
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98%
form
solid
mp
72-75 °C (lit.)
solubility
H2O: slightly soluble
functional group
aldehyde, amine
SMILES string
CN(C)c1ccc(C=O)cc1
InChI
1S/C9H11NO/c1-10(2)9-5-3-8(7-11)4-6-9/h3-7H,1-2H3
InChI key
BGNGWHSBYQYVRX-UHFFFAOYSA-N
General description
4-(Dimethylamino)benzaldehydeis an organic carbonyl compound containing amino and aldehyde groups. The compound is used in Ehrlich and Kovac′s reagents to test indole.4-(Dimethylamino)benzaldehyde is used to prepare aldehydes from Grignard reagents. In addition, it is used as a color test reagent for pyrroles, primary amines, and hydrazines.
Application
Forms colored condensation products (Schiff bases) with pyrroles and primary amines.
4-(Dimethylamino)benzaldehyde was used in the chitinase assay.
4-(Dimethylamino)benzaldehyde is used:
4-(Dimethylamino)benzaldehyde is used:
- In the synthesis of azo-azomethine dyes by condensation reaction.
- As a reagent in the synthesis of molecular adduct 4DMAB4NP (4-(dimethylamino)benzaldehyde 4-nitrophenol) by reacting with 4-nitrophenol.
- In the preparation of Schiff base.
signalword
Warning
hcodes
Hazard Classifications
Skin Sens. 1B
Classe de stockage
11 - Combustible Solids
wgk
WGK 1
flash_point_f
327.2 °F - closed cup
flash_point_c
164 °C - closed cup
ppe
Eyeshields, Gloves, type N95 (US)
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Facile synthesis of Co3O4 and ZnO nanoparticles by thermal decomposition of novel Co (II) and Zn (II) Schiff base complexes for studying their biological properties and photocatalytic degradation of crystal violet dye
Katouah HA
Journal of Molecular Structure, 1241, 130676-130676 (2021)
Synthesis, structural, spectral, third order nonlinear optical and quantum chemical investigations on hydrogen bonded novel organic molecular adduct 4-(dimethylamino) benzaldehyde 4-nitrophenol for opto-electronic applications
Karthick S, et al.
Journal of Molecular Structure, 1178, 352-365 (2019)
M Legrand et al.
Proceedings of the National Academy of Sciences of the United States of America, 84(19), 6750-6754 (1987-10-01)
Four endochitinases (poly[1,4-(N-acetyl-beta-D-glucosaminide)] glycanohydrolase, EC 3.2.1.14) have been purified from leaves of Nicotiana tabacum cv. Samsun NN reacting hypersensitively to tobacco mosaic virus. Two of them are acidic proteins of molecular weights 27,500 and 28,500 and have been identified as