CAS 20870-78-4: 5-Bromooxindole
Formula:C8H6BrNO
InChI:InChI=1S/C8H6BrNO/c9-6-1-2-7-5(3-6)4-8(11)10-7/h1-3H,4H2,(H,10,11)
InChI key:InChIKey=VIMNAEVMZXIKFL-UHFFFAOYSA-N
SMILES:O=C1NC=2C(C1)=CC(Br)=CC2
Synonyms:- 2-Indolinone, 5-bromo-
- 2H-Indol-2-one, 5-bromo-1,3-dihydro-
- 5-Bromo-1,3-dihydro-2H-indol-2-one
- 5-Bromo-1,3-dihydroindol-2-one
- 5-Bromo-2,3-dihydroindol-2-one
- 5-Bromo-2-oxindole
- 5-Bromo-2-oxo-2,3-dihydro-1H-indole
- 5-Bromoindolin-2-One
- 5-bromo-2,3-dihydro-1H-indol-2-one
- Oxindole, 5-bromo-
- Timtec-Bb Sbb005897
Sort by
Found 7 products.
5-Bromooxindole
CAS:Formula:C8H6BrNOPurity:>97.0%(GC)(N)Color and Shape:Light yellow to Yellow to Orange powder to crystalMolecular weight:212.055-Bromooxindole, 97%
CAS:This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.Formula:C8H6BrNOPurity:97%Color and Shape:Off-white to tan, Powder or crystalsMolecular weight:212.055-Bromo-2-oxindole
CAS:5-Bromo-2-oxindoleFormula:C8H6BrNOPurity:By hplc: 95.8% by area (Typical Value in Batch COA)Color and Shape: faint red solidMolecular weight:212.04g/mol5-Bromooxindole, 98%
CAS:5-Bromooxindole is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff. 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 or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.Formula:C8H6BrNOPurity:98%Molecular weight:212.055-Bromooxindole
CAS:5-Bromooxindole is a synthetic compound that is used as a marine sponge extract to study the interaction between cancer and inflammatory diseases. It has been shown to have anti-inflammatory properties, which may be due to its ability to inhibit prostaglandin synthesis. 5-Bromooxindole also inhibits the growth of cancer cells in vitro by suppressing the expression of suppressor genes such as p53, Bax, and caspases. This drug also inhibits the growth of gram-negative bacteria through interactions with their protein targets. Structural isomers of this compound show inhibitory potency against different bacterial strains such as Escherichia coli, Salmonella enterica serovar Typhimurium, Pseudomonas aeruginosa, and Klebsiella pneumoniae. 5-Bromooxindole has been shown to bind to specific sites on DNA, leading to inhibition of DNA replication and transcription. The binding site for this drugFormula:C8H6BrNOPurity:Min. 95%Molecular weight:210.963282H-Indol-2-one, 5-bromo-1,3-dihydro-
CAS:Formula:C8H6BrNOPurity:97%Color and Shape:SolidMolecular weight:212.0433
