2-Ethynyl-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione
98%
- Product Code: 184992
CAS:
1310384-76-9
| Molecular Weight: | 180.95 g./mol | Molecular Formula: | C₇H₈BNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11215242 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, seal, dry |
Product Description:
Used as a specialized boron-containing reagent in organic synthesis, particularly in cyclization and heterocycle formation reactions. Its strained ring structure and alkyne functionality enable participation in transition metal-catalyzed coupling reactions, such as Sonogashira and Diels-Alder reactions, facilitating the construction of complex polycyclic frameworks. Commonly employed in the development of pharmaceutical intermediates and functional materials where precise boron placement is required. Its unique scaffold also shows potential in medicinal chemistry for designing enzyme inhibitors due to its ability to mimic transition states in metabolic pathways.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft27,636.75 |
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| 0.250 | 10-20 days | Ft44,870.32 |
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| 1.000 | 10-20 days | Ft126,099.25 |
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| 5.000 | 10-20 days | Ft529,616.86 |
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2-Ethynyl-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione
Used as a specialized boron-containing reagent in organic synthesis, particularly in cyclization and heterocycle formation reactions. Its strained ring structure and alkyne functionality enable participation in transition metal-catalyzed coupling reactions, such as Sonogashira and Diels-Alder reactions, facilitating the construction of complex polycyclic frameworks. Commonly employed in the development of pharmaceutical intermediates and functional materials where precise boron placement is required. Its unique scaffold also shows potential in medicinal chemistry for designing enzyme inhibitors due to its ability to mimic transition states in metabolic pathways.
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