tert-Butyl N-[3-(tetramethyl-1,3,2-dioxaborolan-2-yl)propyl]carbamate
95%
- Product Code: 65474
CAS:
1850305-80-4
| Molecular Weight: | 285.19 g./mol | Molecular Formula: | C₁₄H₂₈BNO₄ |
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| EC Number: | MDL Number: | MFCD22383765 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C, inert gas |
Product Description:
This chemical is widely used as a key intermediate in organic synthesis, particularly in the preparation of boron-containing compounds. Its primary application lies in the field of medicinal chemistry, where it serves as a building block for the development of pharmaceutical agents, especially those targeting protease enzymes and other biologically relevant molecules. The tetramethyl-1,3,2-dioxaborolane group is particularly valuable in Suzuki-Miyaura cross-coupling reactions, a widely employed method for forming carbon-carbon bonds in drug discovery and materials science. Additionally, it is utilized in the synthesis of boron neutron capture therapy (BNCT) agents, which are used in cancer treatment. The tert-butyl carbamate group provides stability and protection for amines during multi-step synthetic processes, making it a versatile reagent in complex organic transformations.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | €58.41 |
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| 0.250 | 10-20 days | €122.52 |
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| 1.000 | 10-20 days | €272.58 |
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tert-Butyl N-[3-(tetramethyl-1,3,2-dioxaborolan-2-yl)propyl]carbamate
This chemical is widely used as a key intermediate in organic synthesis, particularly in the preparation of boron-containing compounds. Its primary application lies in the field of medicinal chemistry, where it serves as a building block for the development of pharmaceutical agents, especially those targeting protease enzymes and other biologically relevant molecules. The tetramethyl-1,3,2-dioxaborolane group is particularly valuable in Suzuki-Miyaura cross-coupling reactions, a widely employed method for forming carbon-carbon bonds in drug discovery and materials science. Additionally, it is utilized in the synthesis of boron neutron capture therapy (BNCT) agents, which are used in cancer treatment. The tert-butyl carbamate group provides stability and protection for amines during multi-step synthetic processes, making it a versatile reagent in complex organic transformations.
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