Tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-imidazole-1-carboxylate-2,5-d2

95%

Reagent Code: #242076
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CAS Number 2241864-95-7

science Other reagents with same CAS 2241864-95-7

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Weight 296.166743556 g/mol
Formula C₁₄H₂₁BD₂N₂O₄
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description 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.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿133,550.00
inventory 100mg
10-20 days ฿397,830.00

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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
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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 compou

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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