Tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-imidazole-1-carboxylate-2,5-d2
95%
- Product Code: 242076
CAS:
2241864-95-7
| Molecular Weight: | 296.166743556 g./mol | Molecular Formula: | C₁₄H₂₁BD₂N₂O₄ |
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| Density: | Storage Condition: | -20°C, sealed, dry |
Product Description:
Used in organic synthesis as a boronic ester derivative for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. The deuterated labels (2,5-d2) make it valuable in isotopic labeling studies, particularly for tracing metabolic pathways or improving the pharmacokinetic profile of drug candidates. The imidazole core is common in bioactive molecules, making this compound useful in the synthesis of deuterated heterocyclic compounds for medicinal chemistry research. The Boc-protected imidazole allows for controlled deprotection and functionalization, offering selective reactivity in multi-step syntheses.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | $6,322.92 |
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| 0.100 | 10-20 days | $18,835.26 |
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Tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-imidazole-1-carboxylate-2,5-d2
Used in organic synthesis as a boronic ester derivative for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. The deuterated labels (2,5-d2) make it valuable in isotopic labeling studies, particularly for tracing metabolic pathways or improving the pharmacokinetic profile of drug candidates. The imidazole core is common in bioactive molecules, making this compound useful in the synthesis of deuterated heterocyclic compounds for medicinal chemistry research. The Boc-protected imidazole allows for controlled deprotection and functionalization, offering selective reactivity in multi-step syntheses.
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