5-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole
95%
Reagent
Code: #90917
CAS Number
1689539-29-4
science Other reagents with same CAS 1689539-29-4
blur_circular Chemical Specifications
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Molecular Information
Weight
258.12 g/mol
Formula
C₁₄H₁₉BN₂O₂
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Registry Numbers
MDL Number
MFCD28977193
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Storage & Handling
Storage
2-8°C, sealed, dry
description Product Description
This chemical is primarily utilized in the field of organic synthesis, particularly in cross-coupling reactions. It serves as a key intermediate in the preparation of various pharmaceutical compounds, enabling the formation of carbon-carbon and carbon-heteroatom bonds. Its boronic ester functional group makes it valuable in Suzuki-Miyaura coupling reactions, which are widely employed in drug discovery and development. Additionally, it is used in the synthesis of biologically active molecules, including potential therapeutic agents targeting specific diseases. Its stability and reactivity make it a versatile building block in medicinal chemistry and materials science research.
format_list_bulleted Product Specification
| Test Parameter | Specification |
|---|---|
| Appearance | Off-White to Yellow Solid |
| Purity (%) | 94.5-100 |
| Infrared Spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
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