(1R,3S,4S)-tert-Butyl 3-(6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-benzo[d]imidazol-2-yl)-2-azabicyclo[2.2.1]heptane-2-carboxylate
98%
Reagent
Code: #70807
CAS Number
1256387-87-7
blur_circular Chemical Specifications
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Molecular Information
Weight
439.36 g/mol
Formula
C₂₄H₃₄BN₃O₄
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Registry Numbers
MDL Number
MFCD28386938
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Storage & Handling
Storage
2-8°C, store under inert gas
description Product Description
This compound is primarily utilized in organic synthesis, particularly in the field of medicinal chemistry, where it serves as a key intermediate in the development of biologically active molecules. Its structure, featuring a boronic ester group, makes it valuable for Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. This reaction is essential in the synthesis of complex organic compounds, including pharmaceuticals and agrochemicals. Additionally, the bicyclic framework and imidazole moiety in the molecule suggest potential applications in the design of drug candidates targeting various diseases, such as cancer or infectious diseases, due to their ability to interact with biological targets. Its role as a building block in drug discovery highlights its importance in creating novel therapeutic agents.
format_list_bulleted Product Specification
| Test Parameter | Specification |
|---|---|
| Appearance | Off-white to light yellow solid |
| Purity | 95-100 |
| Infrared Spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
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