201014
N-Benzylbenzamid
≥98%
Synonym(e):
Benzoic acid benzylamide, N-(Phenylmethyl)benzamide, N-Benzoylbenzylamine
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Alle Fotos(1)
About This Item
Lineare Formel:
C6H5CONHCH2C6H5
CAS-Nummer:
Molekulargewicht:
211.26
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22
Empfohlene Produkte
Qualitätsniveau
Assay
≥98%
mp (Schmelzpunkt)
104-106 °C (lit.)
Löslichkeit
acetone: 25 mg/mL, clear, colorless
Funktionelle Gruppe
amide
phenyl
SMILES String
O=C(NCc1ccccc1)c2ccccc2
InChI
1S/C14H13NO/c16-14(13-9-5-2-6-10-13)15-11-12-7-3-1-4-8-12/h1-10H,11H2,(H,15,16)
InChIKey
LKQUCICFTHBFAL-UHFFFAOYSA-N
Allgemeine Beschreibung
N-Benzylbenzamide inhibits the activity of tyrosinase.
Anwendung
A convenient precursor to α-substituted benzylamines and an indicator for the titration of butyllithium and other lithium bases. For references see Aldrichimica Acta .
Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 3
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
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Aldrichimica Acta, 11, 20-20 (1978)
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A simple and efficient method is presented for assessing molecularly imprinted polymers (MIP) and other sorbents from the point of view of practical applications. The adsorption isotherms of the compounds, which need to be separated or detected in an application
Sung Jin Cho et al.
Bioorganic & medicinal chemistry letters, 16(10), 2682-2684 (2006-03-04)
A series of potent inhibitors of tyrosinase and their structure-activity relationships are described. N-Benzylbenzamide derivatives (1-21) with hydroxyl(s) were synthesized and tested for their tyrosinase inhibitory activity. With this series, compound 15 provided a potent tyrosinase inhibition: it effectively inhibited
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