72351
Benzyl nicotinate
≥98.0% (GC)
Synonym(s):
Nicotinic acid benzyl ester
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$133.00
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100 ML
$133.00
500 ML
$553.00
About This Item
Empirical Formula (Hill Notation):
C13H11NO2
CAS Number:
Molecular Weight:
213.23
Beilstein/REAXYS Number:
159169
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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assay
≥98.0% (GC)
form
liquid
refractive index
n20/D 1.570
bp
177 °C/8 mmHg (lit.)
mp
24 °C (lit.)
functional group
ester
phenyl
SMILES string
O=C(OCc1ccccc1)c2cccnc2
InChI
1S/C13H11NO2/c15-13(12-7-4-8-14-9-12)16-10-11-5-2-1-3-6-11/h1-9H,10H2
InChI key
KVYGGMBOZFWZBQ-UHFFFAOYSA-N
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General description
Application
Benzyl nicotinate can be used for the synthesis of benzylpalladium complexes to be used as catalysts for the substitution of olefins with benzylic groups.[3]
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
Storage Class
11 - Combustible Solids
wgk_germany
WGK 2
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Ute Jacobi et al.
Archives of dermatological research, 298(6), 291-300 (2006-09-13)
Cutaneous characteristics, e.g., thickness of the SC and density of follicles, affect the penetration of topically applied substances. In the present study, the penetration of benzyl nicotinate, causing a vasodilation, was studied on three anatomic sites (forearm, forehead and calf)
Francesca Palombo et al.
Journal of biomedical optics, 14(4), 044008-044008 (2009-09-04)
Diffusion of two model drugs-benzyl nicotinate and ibuprofen-and the plasma macromolecule albumin across atherosclerotic rabbit aorta was studied ex vivo by attenuated total reflection-Fourier transform infrared (ATR-FTIR) imaging. Solutions of these molecules were applied to the endothelial surface of histological
Zrinka Abramović et al.
International journal of pharmaceutics, 359(1-2), 220-227 (2008-05-13)
Many novel nanosized delivery systems have been designed for topical application of drugs since they can overcome the skin barrier and improve drug bioavailability. The increased absorption is often a consequence of a reversibly disrupted barrier function of the skin
M A Kassem et al.
European journal of drug metabolism and pharmacokinetics, 5(1), 25-28 (1980-01-01)
The effect of benzyl nicotinate (15 mg) on the percutaneous absorption of dexamethasone 0,1 mg (62,5 uCi)/6 cm2, in an ethanol/octanol vehicle has been investigated in the rat. Both the urinary excretion and blood concentration data showed that benzyl nicotinate
Nadeau Christian et al.
Journal of the American Chemical Society, 133(9), 2878-2880 (2011-02-12)
The highly enantioselective catalytic asymmetric addition of aryl and alkenylboronic acids to N-benzylnicotinate salt 1 is described. The dihydropyridine 2 reaction products can be converted to synthetically useful piperidines. Application of the methodology to the preparation of enantioenriched quaternary chiral
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