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  4. N-Boc-5-bromoindole

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.

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N-Boc-5-bromoindole Chemical Structure

N-Boc-5-bromoindole Chemical Structure

CAS No. : 182344-70-3

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Description

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].

Molecular Weight

296.16

Formula

C13H14BrNO2
CAS No.
Appearance

Solid

SMILES

O=C(OC(C)(C)C)N1C=CC2=C1C=CC(Br)=C2
Shipping

Room temperature in continental US; may vary elsewhere.
Storage
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
Purity & Documentation

Purity: 99.98%

SDS (393 KB)

COA (252 KB) HNMR (134 KB) RP-HPLC (195 KB)

Handling Instructions (2659 KB)
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N-Boc-5-bromoindole Related Classifications

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This equation is commonly abbreviated as: C1V1 = C2V2

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× = ×
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  • Do most proteins show cross-species activity?

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Keywords:

N-Boc-5-bromoindole182344-70-3OthersInhibitorinhibitorinhibit

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