(N-Boc-5-bromo-2-indolyl)boronic acid
95%
Reagent
Code: #91011
Alias
N-Boc-5-bromoindole-2-boronic acid
1-(tert-butoxycarbonyl-5-bromo-1H-indol-2-yl)boronic acid
CAS Number
475102-13-7
blur_circular Chemical Specifications
scatter_plot
Molecular Information
Weight
339.98 g/mol
Formula
C₁₃H₁₅BBrNO₄
badge
Registry Numbers
MDL Number
MFCD03701683
thermostat
Physical Properties
Melting Point
93 °C
inventory_2
Storage & Handling
Density
1.45
Storage
2~8°C
description Product Description
This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. It serves as a key intermediate in the preparation of complex indole derivatives, which are important in pharmaceutical research and drug development. The N-Boc protecting group ensures stability during reactions, while the boronic acid moiety facilitates coupling with aryl or vinyl halides. Its application extends to the synthesis of biologically active compounds, including potential anticancer and anti-inflammatory agents. The bromo substituent on the indole ring allows for further functionalization, making it a versatile building block in medicinal chemistry.
format_list_bulleted Product Specification
| Test Parameter | Specification |
|---|---|
| Purity | 95-100% |
| Appearance | White to light brown powder |
shopping_cart Available Sizes & Pricing
Cart
No products
Subtotal:
0.00
Total
0.00
THB