CAS 59-48-3
:Oxindole
Description:
Oxindole is an organic compound characterized by its bicyclic structure, which consists of an indole ring fused to a carbonyl group. It is a white to off-white crystalline solid that is soluble in organic solvents such as ethanol and chloroform but has limited solubility in water. The molecular formula of oxindole is C8H7NO, and it features a nitrogen atom within the indole framework, contributing to its basic properties. Oxindole is known for its role in various biological activities, including potential applications in pharmaceuticals, where it serves as a scaffold for the development of drugs targeting neurological disorders and other conditions. Additionally, it can participate in various chemical reactions, such as electrophilic substitutions and cyclizations, making it a valuable intermediate in organic synthesis. Its derivatives have been studied for their anti-inflammatory, analgesic, and antitumor properties, highlighting the compound's significance in medicinal chemistry. Overall, oxindole is a versatile compound with important implications in both research and industry.
Formula:C8H7NO
InChI:InChI=1S/C8H7NO/c10-8-5-6-3-1-2-4-7(6)9-8/h1-4H,5H2,(H,9,10)
InChI key:InChIKey=JYGFTBXVXVMTGB-UHFFFAOYSA-N
SMILES:O=C1CC=2C(N1)=CC=CC2
Synonyms:- 1,3-Dihydroindol-2-one
- 1,3-dihydro-2H-indol-2-one
- 2,3-Dihidroindol-2-Ona
- 2,3-Dihydro-1H-indol-2-one
- 2,3-Dihydroindol-2-One
- 2,3-Dihydroindol-2-on
- 2,3-Dihydroindole-2-One
- 2-Indolinone
- 2-Indolone
- 2-Oxindole
- 2-Oxo-2,3-dihydroindole
- 2-Oxoindole
- 2-Oxoindoline
- 2H-Indol-2-one, 1,3-dihydro-
- Indol-2(3H)-one
- Indolin-2-one
- Indoline-2-one
- Nsc 274863
- O-(Aminophenyl)Acetic acid Lactam
- Oxidinole (Indolin-2-One)
- Oxindol
- Timtec-Bb Sbb004215
- See more synonyms
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Found 16 products.
Oxindole
CAS:Formula:C8H7NOPurity:>98.0%(GC)Color and Shape:White to Light yellow to Light orange powder to crystalMolecular weight:133.15Oxindole, 97+%
CAS:<p>Oxindole is considered as indole analogue, which shows pharmacological activity. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code</p>Formula:C8H7NOPurity:97+%Color and Shape:White to dark cream to cream to brown, PowderMolecular weight:133.15Oxindole
CAS:<p>Lactams, nesoi</p>Formula:C8H7NOColor and Shape:White Crystalline PowderMolecular weight:133.05276Oxindole
CAS:<p>Oxindole (Indolin-2-one) is an aromatic heterocyclic building block.</p>Formula:C8H7NOPurity:97.42% - 99.65%Color and Shape:Off-White Crystalline PowderMolecular weight:133.152-Oxindole
CAS:<p>2-Oxindole</p>Formula:C8H7NOPurity:98%Color and Shape: light orange powderMolecular weight:133.15g/molDiclofenac EP Impurity E (Oxindole)
CAS:Formula:C8H7NOColor and Shape:Brown SolidMolecular weight:133.15Oxindole
CAS:Formula:C8H7NOPurity:(HPLC) ≥ 97.0%Color and Shape:White to light yellow or light orange crystalline powderMolecular weight:133.15Oxindole (2-Indolone)
CAS:Controlled Product<p>Applications Indole analogue; shows pharmacological activity.<br>References Mohammadi, M., et al.: Science, 276, 955 (1997), Bramson, H., et al.: J. Med. Chem., 44, 4339 (2001), Lane, M., et al.: Cancer Res., 61, 6170 (2001), Yu, B., et al.: Biochem. Pharmacol., 64, 1091 (2002),<br></p>Formula:C8H7NOColor and Shape:Light RedMolecular weight:133.152-Indolone
CAS:<p>2-Indolone is a synthetic compound that belongs to the class of heterocyclic compounds. It is a trifluoroacetic acid derivative that has been shown to have potent antitumor activity, and it also inhibits cell proliferation. 2-Indolone has been shown to be an effective treatment for inflammatory diseases such as rheumatoid arthritis and Crohn's disease. This compound has been shown to bind to response elements in the promoter region of genes in the basic fibroblast line, and this binding leads to increased expression of gene products involved in inflammation and tumor suppression. The reaction mechanism for 2-indolone involves a two-step process, with activation energies for both steps being high. The first step involves protonation of the C2 hydroxyl group by trifluoroacetic acid, which leads to its displacement by hydrogen from water molecule H2O. In the second step, the oxindole ring opens up, with displacement of</p>Formula:C8H7NOPurity:Min. 95%Color and Shape:PowderMolecular weight:133.15 g/mol1,3-Dihydro-2H-indol-2-one
CAS:Formula:C8H7NOPurity:97%Color and Shape:Solid, Chunks or Crystalline PowderMolecular weight:133.15Oxindole
CAS:<p>Oxindole (Indolin-2-one) is an aromatic heterocyclic building block. 2-indolinone derivatives have become lead compounds in the research of kinase inhibitors.Oxindole structure has been used in receptor tyrosine kinases (RTKs) inhibitors such as SU4984 and intedanib, the RTK family represents an important therapeutic target for anti-cancer drug development.</p>Formula:C8H7NOPurity:99.34%Color and Shape:Off-White Crystalline PowderMolecular weight:133.15














