N,N-Dimethyl-N'-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]sulfamide
95%
- Product Code: 50572
CAS:
1301190-20-4
| Molecular Weight: | 326.22 g./mol | Molecular Formula: | C₁₄H₂₃BN₂O₄S |
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| Density: | Storage Condition: | 2-8℃ |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in the development of pharmaceuticals and biologically active compounds. Its structure, featuring a dioxaborolane group, makes it a valuable intermediate in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in drug discovery and material science. Additionally, the sulfamide moiety in its structure can contribute to its potential use in designing enzyme inhibitors or receptor modulators, particularly in medicinal chemistry research. Its applications also extend to the synthesis of advanced materials, where its boronate ester functionality can be leveraged for polymer modification or functionalization.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.050 | 10-20 days | $191.18 |
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| 0.250 | 10-20 days | $636.18 |
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| 1.000 | 10-20 days | $1,730.33 |
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N,N-Dimethyl-N'-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]sulfamide
This chemical is primarily utilized in organic synthesis, particularly in the development of pharmaceuticals and biologically active compounds. Its structure, featuring a dioxaborolane group, makes it a valuable intermediate in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in drug discovery and material science. Additionally, the sulfamide moiety in its structure can contribute to its potential use in designing enzyme inhibitors or receptor modulators, particularly in medicinal chemistry research. Its applications also extend to the synthesis of advanced materials, where its boronate ester functionality can be leveraged for polymer modification or functionalization.
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