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7127-19-7 | 2-Phenyl-4,5-dihydrooxazole
CAS No: 7127-19-7 Catalog No: AG003KI0 MDL No:MFCD00075541
Product Description
Catalog Number:
AG003KI0
Chemical Name:
2-Phenyl-4,5-dihydrooxazole
CAS Number:
7127-19-7
Molecular Formula:
C9H9NO
Molecular Weight:
147.1739
MDL Number:
MFCD00075541
IUPAC Name:
2-phenyl-4,5-dihydro-1,3-oxazole
InChI:
InChI=1S/C9H9NO/c1-2-4-8(5-3-1)9-10-6-7-11-9/h1-5H,6-7H2
InChI Key:
ZXTHWIZHGLNEPG-UHFFFAOYSA-N
SMILES:
c1ccc(cc1)C1=NCCO1
Properties
Complexity:
159
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
147.068g/mol
Formal Charge:
0
Heavy Atom Count:
11
Hydrogen Bond Acceptor Count:
2
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
147.177g/mol
Monoisotopic Mass:
147.068g/mol
Rotatable Bond Count:
1
Topological Polar Surface Area:
21.6A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.5
Literature
| Title | Journal |
|---|---|
| Synthesis of poly(2-oxazoline)-based hydrogels with tailor-made swelling degrees capable of stimuli-triggered compound release. | Macromolecular rapid communications 20111115 |
| Characterisation of different nanoparticles with a potential use for drug delivery in neuropsychiatric disorders. | The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry 20110901 |
| Solute-solvent friction kernels and solution properties of methyl oxazoline-phenyl oxazoline (MeOx-PhOx) copolymers in binary ethanol-water mixtures. | Physical chemistry chemical physics : PCCP 20110707 |
| The first oxazoline adduct of Zn(acac)(2): bis-(acetyl-acetonato-κO,O')(2-phenyl-2-oxazoline-κN)zinc(II). | Acta crystallographica. Section E, Structure reports online 20090101 |
| Pre-catalyst resting states: a kinetic, thermodynamic and quantum mechanical analyses of [PdCl2(2-oxazoline)2] complexes. | Dalton transactions (Cambridge, England : 2003) 20080621 |
| Estimation of the hydrophobicity of 2,4-diphenyl-1,3-oxazoline analogs and QSAR analysis of their ovicidal activity against Tetranychus [corrected] urticae. | Bioorganic & medicinal chemistry letters 20060801 |
| Atropisomeric discrimination in new Ru(II) complexes containing the C(2)-symmetric didentate chiral phenyl-1,2-bisoxazolinic ligand. | Chemistry (Weinheim an der Bergstrasse, Germany) 20060320 |
| Sector spin coating for fast preparation of polymer libraries. | Journal of combinatorial chemistry 20050101 |
| Enzymatic synthesis of chondroitin and its derivatives catalyzed by hyaluronidase. | Journal of the American Chemical Society 20031126 |
| On the intermediates in chiral bis(oxazoline)copper(II)-catalyzed enantioselective reactions--experimental and theoretical investigations. | Chemistry (Weinheim an der Bergstrasse, Germany) 20020415 |
| Unprecedented chiral molecular recognition in a C3-symmetric environment. | Journal of the American Chemical Society 20020130 |
| Enantioselective hydrogenations of arylalkenes mediated by [Ir(cod) (JM-Phos) ]+ complexes. | Chemistry (Weinheim an der Bergstrasse, Germany) 20011217 |
| New, optically active phosphine oxazoline (JM-Phos) ligands: syntheses and applications in allylation reactions. | The Journal of organic chemistry 20010112 |
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