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5-Bromo-2-oxindole

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5-Bromo-2-oxindole manufacturers

  • 5-Bromo-2-oxindole
  • 5-Bromo-2-oxindole pictures
  • 2025-04-04
  • CAS:20870-78-4
  • Min. Order: 1KG
  • Purity: 98%
  • Supply Ability: 1ton
5-Bromo-2-oxindole Basic information
Preparation
Product Name:5-Bromo-2-oxindole
Synonyms:TIMTEC-BB SBB005897;5-Bromo-2-oxindole 97%;5-BroMo-2-oxindole , tech;5-BROMO-1,3-DIHYDRO-2H-INDOL-2-ONE;5-BROMO-1,3-DIHYDRO-INDOL-2-ONE;5-BROMOOXINDOLE;5-BROMO-2-INDOLINONE;5-BROMO-2,3-DIHYDRO-1H-INDOL-2-ONE
CAS:20870-78-4
MF:C8H6BrNO
MW:212.04
EINECS:626-894-8
Product Categories:blocks;Bromides;IndolesOxindoles;Indoles and derivatives;Indoline & Oxindole;Indoles;Halogenated Heterocycles;Heterocyclic Building Blocks;IndolesBuilding Blocks;Heterocycles;Boronic Acid;Heterocyclic Compounds;oxindoles
Mol File:20870-78-4.mol
5-Bromo-2-oxindole Structure
5-Bromo-2-oxindole Chemical Properties
Melting point 220-224 °C(lit.)
Boiling point 362.5±42.0 °C(Predicted)
density 1.666±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility Soluble in Dimethylformamide.
pka13.27±0.20(Predicted)
form Powder, Crystals or Granules
color Yellow to orange to gold
InChIInChI=1S/C8H6BrNO/c9-6-1-2-7-5(3-6)4-8(11)10-7/h1-3H,4H2,(H,10,11)
InChIKeyVIMNAEVMZXIKFL-UHFFFAOYSA-N
SMILESN1C2=C(C=C(Br)C=C2)CC1=O
CAS DataBase Reference20870-78-4(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 36-43-36/37/38-20/21/22
Safety Statements 26-36/37-36/37/39-22
WGK Germany 3
HazardClass IRRITANT
HS Code 29337900
Storage Class11 - Combustible Solids
Hazard ClassificationsEye Irrit. 2
Skin Sens. 1
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
5-Bromo-2-oxindole Usage And Synthesis
PreparationAdd 2.5 equal volumes of phosphorus oxychloride dropwise to dimethylformamide (5 ml per 1 ml POCl3), and cool in an ice bath. Stir the mixture for 5 minutes. Add the selected indole (1 equal volume) as a dimethylformamide solution (10 ml per 1 g indole). Heat the mixture to room temperature. Stir the mixture for 3 hours. When the reaction becomes a heavy suspension requiring vigorous stirring, add 10 equal volumes of 3.8 M potassium hydroxide aqueous solution through a dropping funnel. Heat the mixture under reflux overnight. Cool the mixture to room temperature. Add saturated sodium bicarbonate and ethyl acetate until the mixture becomes clear. Separate the organic layer. Extract the aqueous layer with ethyl acetate. Dry the combined organic layer on sodium sulfate. Filter the combined organic layer. Concentrate the combined organic layer under vacuum to give the title compound 5-Bromo-2-oxindole.
Chemical PropertiesWhite to brown crytalline powder
Uses5-Bromooxindole is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff.
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