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Home > Indoles and Oxindole > 6786-41-0
6786-41-0 | Spiro[indoline-3,3'-pyrrolidin]-2-one
CAS No: 6786-41-0 Catalog No: AG005P83 MDL No:MFCD17019392
Product Description
Catalog Number:
AG005P83
Chemical Name:
Spiro[indoline-3,3'-pyrrolidin]-2-one
CAS Number:
6786-41-0
Molecular Formula:
C11H12N2O
Molecular Weight:
188.2258
MDL Number:
MFCD17019392
IUPAC Name:
spiro[1H-indole-3,3'-pyrrolidine]-2-one
InChI:
InChI=1S/C11H12N2O/c14-10-11(5-6-12-7-11)8-3-1-2-4-9(8)13-10/h1-4,12H,5-7H2,(H,13,14)
InChI Key:
FQSHLSLQUHZOMV-UHFFFAOYSA-N
SMILES:
O=C1Nc2c(C31CNCC3)cccc2
Properties
Complexity:
266
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
188.095g/mol
Formal Charge:
0
Heavy Atom Count:
14
Hydrogen Bond Acceptor Count:
2
Hydrogen Bond Donor Count:
2
Isotope Atom Count:
0
Molecular Weight:
188.23g/mol
Monoisotopic Mass:
188.095g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
41.1A^2
Undefined Atom Stereocenter Count:
1
Undefined Bond Stereocenter Count:
0
XLogP3:
0.3
Literature
| Title | Journal |
|---|---|
| Domino Pd-catalyzed Heck cyclization and bismuth-catalyzed hydroamination: formal synthesis of elacomine and isoelacomine. | Chemistry (Weinheim an der Bergstrasse, Germany) 20110110 |
| Organocatalytic synthesis of spiro[pyrrolidin-3,3'-oxindoles] with high enantiopurity and structural diversity. | Journal of the American Chemical Society 20090930 |
| Total synthesis of (-)-spirotryprostatin B: synthesis and related studies. | Journal of the American Chemical Society 20050817 |
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