(5-(((tert-Butoxycarbonyl)amino)methyl)thiophen-2-yl)boronic acid
≥98%
Reagent
Code: #90859
CAS Number
1072951-39-3
science Other reagents with same CAS 1072951-39-3
blur_circular Chemical Specifications
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Molecular Information
Weight
257.11 g/mol
Formula
C₁₀H₁₆BNO₄S
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Registry Numbers
MDL Number
MFCD11504845
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Storage & Handling
Storage
-20°C, protected from light, stored under inert gas
description Product Description
This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the production of complex organic molecules, including pharmaceuticals and agrochemicals. The boronic acid group enables the formation of carbon-carbon bonds, making it valuable in constructing biologically active compounds. Additionally, the tert-butoxycarbonyl (Boc) protecting group ensures selective reactivity during multi-step synthesis processes. Its application extends to materials science, where it aids in the development of advanced polymers and functional materials.
format_list_bulleted Product Specification
| Test Parameter | Specification |
|---|---|
| Appearance | White to off-white Solid |
| Purity (%) | 98-100 |
| Infrared Spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
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