Cas no 1343500-43-5 (1H-Indole-1-carboxylic acid, 5-bromo-2,3-dihydro-2,3-dioxo-, 1,1-dimethylethyl ester)

1H-Indole-1-carboxylic acid, 5-bromo-2,3-dihydro-2,3-dioxo-, 1,1-dimethylethyl ester structure
1343500-43-5 structure
Product Name:1H-Indole-1-carboxylic acid, 5-bromo-2,3-dihydro-2,3-dioxo-, 1,1-dimethylethyl ester
CAS No:1343500-43-5
MF:C13H12BrNO4
MW:326.142683029175
CID:6637806
Update Time:2024-01-15

1H-Indole-1-carboxylic acid, 5-bromo-2,3-dihydro-2,3-dioxo-, 1,1-dimethylethyl ester Chemical and Physical Properties

Names and Identifiers

    • 1H-Indole-1-carboxylic acid, 5-bromo-2,3-dihydro-2,3-dioxo-, 1,1-dimethylethyl ester
    • Inchi： 1S/C13H12BrNO4/c1-13(2,3)19-12(18)15-9-5-4-7(14)6-8(9)10(16)11(15)17/h4-6H,1-3H3
    • InChI Key： KFOIHJWCNOVHMC-UHFFFAOYSA-N
    • SMILES： N1(C(OC(C)(C)C)=O)C2=C(C=C(Br)C=C2)C(=O)C1=O

Experimental Properties

  • Density: 1.583±0.06 g/cm3(Predicted)
  • Boiling Point: 417.9±47.0 °C(Predicted)
  • pka: -4.32±0.20(Predicted)

1H-Indole-1-carboxylic acid, 5-bromo-2,3-dihydro-2,3-dioxo-, 1,1-dimethylethyl ester Production Method

Production Method 1

Reaction Conditions
1.1 Reagents: N-Iodosuccinimide ,  2-Iodoxybenzoic acid Solvents: Dimethyl sulfoxide ;  3 h, 25 °C
Reference
Facile synthesis of isatins by direct oxidation of indoles and 3-iodoindoles using NIS/IBX
Chandra, Ajeet; et al, Tetrahedron, 2019, 75(14), 2169-2174

1H-Indole-1-carboxylic acid, 5-bromo-2,3-dihydro-2,3-dioxo-, 1,1-dimethylethyl ester Raw materials

1H-Indole-1-carboxylic acid, 5-bromo-2,3-dihydro-2,3-dioxo-, 1,1-dimethylethyl ester Preparation Products

1H-Indole-1-carboxylic acid, 5-bromo-2,3-dihydro-2,3-dioxo-, 1,1-dimethylethyl ester Related Literature

1343500-43-5 (1H-Indole-1-carboxylic acid, 5-bromo-2,3-dihydro-2,3-dioxo-, 1,1-dimethylethyl ester) Related Products

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