(4-(((Benzyloxy)carbonyl)(ethyl)amino)phenyl)boronic acid
98%
Reagent
Code: #89175
CAS Number
1221448-69-6
blur_circular Chemical Specifications
scatter_plot
Molecular Information
Weight
299.13 g/mol
Formula
C₁₆H₁₈BNO₄
badge
Registry Numbers
MDL Number
MFCD21609545
inventory_2
Storage & Handling
Storage
2-8°C, inert gas
description Product Description
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid group enables it to form stable bonds with various organic compounds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it serves as a key intermediate in the development of biologically active molecules, aiding in drug discovery and medicinal chemistry research. Its benzyloxycarbonyl protecting group ensures selective reactivity in multi-step synthetic processes.
shopping_cart Available Sizes & Pricing
(4-(((Benzyloxy)carbonyl)(ethyl)amino)phenyl)boronic acid
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid group enables it to form stable bonds with various organic compounds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it serves as a key intermediate in the development of biologically active molecules, aiding in drug discovery and medicinal chemistry research. Its benzyloxycarbonyl protecting group ensures selective reactivity in multi-step synthetic processes.
Mechanism | - |
Appearance | - |
Longevity | - |
Strength | - |
Storage | - |
Shelf Life | - |
Allergen(s) | - |
Dosage (Range) | - |
Recommended Dosage | - |
Dosage (Per Day) | - |
Recommended Dosage (Per Day) | - |
Mix Method | - |
Heat Resistance | - |
Stable in pH range | - |
Solubility | - |
Product Types | - |
INCI | - |
Purchase History for
Loading purchase history...
Cart
No products
Subtotal:
฿0.00
Total
฿0.00
THB