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202191-12-6 | Quinoline, 2-(4,5-dihydro-2-oxazolyl)-
CAS No: 202191-12-6 Catalog No: AG002843 MDL No:MFCD00183217
Product Description
Catalog Number:
AG002843
Chemical Name:
Quinoline, 2-(4,5-dihydro-2-oxazolyl)-
CAS Number:
202191-12-6
Molecular Formula:
C12H10N2O
Molecular Weight:
198.2206
MDL Number:
MFCD00183217
IUPAC Name:
2-quinolin-2-yl-4,5-dihydro-1,3-oxazole
InChI:
InChI=1S/C12H10N2O/c1-2-4-10-9(3-1)5-6-11(14-10)12-13-7-8-15-12/h1-6H,7-8H2
InChI Key:
USDSJWOYSHFPND-UHFFFAOYSA-N
SMILES:
C1CN=C(O1)c1ccc2c(n1)cccc2
Properties
Complexity:
264
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
198.079g/mol
Formal Charge:
0
Heavy Atom Count:
15
Hydrogen Bond Acceptor Count:
3
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
198.225g/mol
Monoisotopic Mass:
198.079g/mol
Rotatable Bond Count:
1
Topological Polar Surface Area:
34.5A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.1
Literature
| Title | Journal |
|---|---|
| Palladium-catalyzed allylic cross-coupling reactions of primary and secondary homoallylic electrophiles. | Journal of the American Chemical Society 20120718 |
| On the mechanism of the palladium-catalyzed tert-butylhydroperoxide-mediated Wacker-type oxidation of alkenes using quinoline-2-oxazoline ligands. | Journal of the American Chemical Society 20110601 |
| Catalyst-controlled Wacker-type oxidation of homoallylic alcohols in the absence of protecting groups. | The Journal of organic chemistry 20110506 |
| 2-(4,5-Dihydro-1,3-oxazol-2-yl)quinoline. | Acta crystallographica. Section E, Structure reports online 20080101 |
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