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Dokumente

O9808

Sigma-Aldrich

2-Indolinon

97%

Synonym(e):

2-Oxindol, Oxindol

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About This Item

Empirische Formel (Hill-System):
C8H7NO
CAS-Nummer:
59-48-3
Molekulargewicht:
133.15
Beilstein:
114692
EG-Nummer:
200-429-5
MDL-Nummer:
MFCD00005711
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24898074
NACRES:
NA.22

Assay

97%

Form

crystals

bp

227 °C/73 mmHg (lit.)

mp (Schmelzpunkt)

123-128 °C (lit.)

SMILES String

O=C1Cc2ccccc2N1

InChI

1S/C8H7NO/c10-8-5-6-3-1-2-4-7(6)9-8/h1-4H,5H2,(H,9,10)

InChIKey

JYGFTBXVXVMTGB-UHFFFAOYSA-N

Angaben zum Gen

human ... PGR(5241)

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Verwandte Kategorien

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

Analysenzertifikate (COA)

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5-(trifluoromethyl)oxindole AldrichCPR

Sigma-Aldrich

CDS008597

5-(trifluoromethyl)oxindole

Isatin 97%

Sigma-Aldrich

114618

Isatin

Yong-Jin Wua et al.
Current medicinal chemistry, 12(4), 453-460 (2005-02-22)
During the past five years, several members of the KCNQ potassium channel gene family have been identified with a high degree of CNS specificity. Within the KCNQ family, the combination of the KCNQ2/KCNQ3 proteins, and the KCNQ5/KCNQ3 arrangement has been
Morteza Bararjanian et al.
The Journal of organic chemistry, 75(9), 2806-2812 (2010-04-15)
An efficient palladium-catalyzed protocol for the synthesis of 3-arylidene-2-oxindoles has been developed. In this approach, a sequential one-pot six-component reaction via Ugi/Heck carbocyclization/Sonogashira/nucleophilic addition was used for the synthesis of the desired skeleton.
C Lanzi et al.
International journal of cancer, 85(3), 384-390 (2000-02-01)
ret-derived oncogenes are frequently and specifically expressed in thyroid tumors. In contrast to the ret receptor, ret oncoproteins are characterized by ligand-independent tyrosine-kinase activity and tyrosine phosphorylation. In this study, novel synthetic arylidene 2-indolinone compounds were evaluated as inhibitors of
Xianjie Chen et al.
Organic letters, 15(8), 1846-1849 (2013-04-09)
An asymmetric organo- and gold-catalyzed one-pot sequential Mannich/hydroamination reaction has been developed. Using this protocol, spiro[pyrrolidin-3,2'-oxindole] derivatives were synthesized in good yields (up to 91%) and excellent enantioselectivities (up to 97% ee).
Fangrui Zhong et al.
Organic letters, 13(1), 82-85 (2010-12-09)
The first tertiary amine catalyzed enantioselective Morita-Baylis-Hillman (MBH) reaction of isatins with acrylates has been demonstrated, allowing asymmetric synthesis of biologically significant 3-substituted-3-hydroxy-2-oxindoles in good yields and with excellent enantioselectivities. The C6'-OH group of β-isocupreidine (β-ICD) is believed to facilitate
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