| Bioactivity | N-Boc-5-bromoindole is formed as an intermediate for the synthesis of di-Boc-protected 5-aminoindole via a Buchwald-Hartwig amination with tBu-carbamate followed by regioselective bromination[1]. | ||||||||||||
| CAS | 182344-70-3 | ||||||||||||
| Formula | C13H14BrNO2 | ||||||||||||
| Molar Mass | 296.16 | ||||||||||||
| Appearance | 固体 | ||||||||||||
| Transport | Room temperature in continental US; may vary elsewhere. | ||||||||||||
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| Reference | [1]. Christoffer Bengtsson, et al. Rapid Construction of a Chloromethyl-Substituted Duocarmycin-like Prodrug. Molecules. 2023 Jun 16;28(12):4818. |
N-Boc-5-bromoindole
CAS: 182344-70-3 F: C13H14BrNO2 W: 296.16
N-Boc-5-bromoindole is formed as an intermediate for the synthesis of di-Boc-protected 5-aminoindole via a Buchwald-Hart
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