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N-Boc-5-bromoindole (97%)

N-Boc-5-bromoindole (97%)

Catalog Number:
CBB1133487
Mfr. No.:
557749
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  • Size:
    25g
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      • Overview

        • N-Boc-5-bromoindole can undergo Sonogashira coupling reaction with N,N-diisopropylprop-2-ynylamine to afford the corresponding propargylic diisopropylamine. N-Boc-5-bromoindole is formed as an intermediate during the synthesis of 2-(5-substituted-1H-indol-3-yl)-N-hydroxyacetamide derivatives.

          Please contact us at for specific academic pricing.

      • Properties
        • Categories
          Halogenated Heterocycles
          Alternative Name
          tert-Butyl 5-bromoindole-1-carboxylate
          CAS Number
          182344-70-3
          Molecular Formula
          C13H14BrNO2
          Molecular Weight
          296.16
          Purity
          97%
          SMILES
          CC(C)(C)OC(=O)n1ccc2cc(Br)ccc12
          InChi
          1S/C13H14BrNO2/c1-13(2,3)17-12(16)15-7-6-9-8-10(14)4-5-11(9)15/h4-8H,1-3H3
          InChi Key
          PBWDRTGTQIXVBR-UHFFFAOYSA-N
          MDL Number
          MFCD02090067
          Others
          SID 24879694
          Hazard Information
          Warning
          Combustible Solids
          Note
          Please note that Amerigo Scientific does not collect analytical data for this product. Buyer assumes responsibility to confirm product identity and/or purity. All sales are final.

          * For Research Use Only.

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