tert-butyl N-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]carbamate
98%
Reagent
Code: #91007
CAS Number
330793-01-6
science Other reagents with same CAS 330793-01-6
blur_circular Chemical Specifications
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Molecular Information
Weight
319.21 g/mol
Formula
C₁₇H₂₆BNO₄
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Registry Numbers
MDL Number
MFCD02179439
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Physical Properties
Melting Point
167-170 °C
Boiling Point
421.6°C
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Storage & Handling
Density
1.06g/mL
Storage
2-8°C
description Product Description
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in pharmaceutical research and development. The boronate ester group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. Its application is crucial in the synthesis of biologically active compounds, including drug candidates and agrochemicals. Additionally, it is employed in material science for creating advanced polymers and organic electronic materials.
format_list_bulleted Product Specification
| Test Parameter | Specification |
|---|---|
| Appearance (Color) | White to Off-White |
| Appearance Form | Powder or Crystals |
| Infrared Spectrum | Conforms to Structure |
| Purity | 97.5-100% |
| Melting Point | 168-172 |
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