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Merck

225681

4-(Diethylamino)salicylaldehyde

98%

Sinónimos:

4-Diethylamino-2-hydroxybenzaldehyde

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Fórmula lineal:
(C2H5)2NC6H3-2-(OH)CHO
Número CAS:
Peso molecular:
193.24
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
241-745-3
MDL number:
Assay:
98%
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Quality Level

assay

98%

mp

60-62 °C (lit.)

functional group

aldehyde, amine

SMILES string

CCN(CC)c1ccc(C=O)c(O)c1

InChI

1S/C11H15NO2/c1-3-12(4-2)10-6-5-9(8-13)11(14)7-10/h5-8,14H,3-4H2,1-2H3

InChI key

XFVZSRRZZNLWBW-UHFFFAOYSA-N

Application

4-(Diethylamino)salicylaldehyde was used in the synthesis of Schiff-base ligand by monocondensation with diaminomaleonitrile.


pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Clase de almacenamiento

11 - Combustible Solids

wgk

WGK 2

ppe

dust mask type N95 (US), Eyeshields, Gloves



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Jean Pierre Costes et al.
Inorganic chemistry, 44(6), 1973-1982 (2005-03-15)
An H2L Schiff-base ligand that was obtained from the monocondensation of diaminomaleonitrile and 4-(diethylamino)salicylaldehyde is reported together with four related nickel(II) complexes formulated as [Ni(L)(L')] (L' = MePhCHNH2, iPrNH2, Py, and PPh3). Crystal structures have been solved for H2L, [Ni(L)(MePhCHNH2)]
Takahiro Nomoto et al.
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In the current clinical boron neutron capture therapy (BNCT), p-boronophenylalanine (BPA) has been the most powerful drug owing to its ability to accumulate selectively within cancers through cancer-related amino acid transporters including LAT1. However, the therapeutic success of BPA has