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About This Item
Empirical Formula (Hill Notation):
C14H15NO
CAS Number:
Molecular Weight:
213.28
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
95%
form
solid
mp
58-65 °C (lit.)
SMILES string
[O-][n+]1ccc(CCCc2ccccc2)cc1
InChI
1S/C14H15NO/c16-15-11-9-14(10-12-15)8-4-7-13-5-2-1-3-6-13/h1-3,5-6,9-12H,4,7-8H2
InChI key
OOFBEJNEUVLZOW-UHFFFAOYSA-N
General description
4-(3-Phenylpropyl)pyridine N-oxide (P3NO, 4-PPPyNO) participates in catalytic media for manganese-salen complex in the asymmetric epoxidation of indene.
Application
4-(3-Phenylpropyl)pyridine N-oxide may be employed as a donor ligand in the managnese-salen complex catalyzed asymmetric epoxidation of indene and styrene.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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David L. Hughes et al.
The Journal of organic chemistry, 62(7), 2222-2229 (1997-04-04)
The asymmetric epoxidation of indene using aqueous NaOCl, catalyzed by Jacobsen's chiral manganese salen complex, provides indene oxide in 90% yield and 85-88% enantioselectivity. The axial ligand, 4-(3-phenylpropyl)pyridine N-oxide (P(3)NO), increases the rate of epoxidation without affecting enantioselectivity and also
The role of 4-(3-phenylpropyl) pyridine N-Oxide (P3NO) in the manganese-salen-catalyzed asymmetric epoxidation of indene.
Senanayake CH, et al.
Tetrahedron Letters, 37(19), 3271-3274 (1996)
Easily recyclable polymeric ionic liquid-functionalized chiral salen Mn (III) complex for enantioselective epoxidation of styrene.
Tan R, et al.
J. Catal., 263(2), 284-291 (2009)
A novel polymeric chiral salen Mn (III) complex as solvent-regulated phase transfer catalyst in the asymmetric epoxidation of styrene.
Tan R, et al.
J. Mol. Catal. A: Chem., 259(1), 125-132 (2006)
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