Tert-butyl 3-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiazol-2-yl)pyrrolidine-1-carboxylate

95%

Reagent Code: #242067
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CAS Number 2223006-38-8

science Other reagents with same CAS 2223006-38-8

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Weight 380.30986 g/mol
Formula C₁₈H₂₉BN₂O₄S
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

Used in organic synthesis as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds for constructing complex molecules, particularly in pharmaceutical and agrochemical research. The boronate ester group facilitates coupling with aryl or heteroaryl halides under palladium catalysis, while the Boc-protected pyrrolidine allows for further functionalization of nitrogen-containing heterocycles. Its structure supports the development of bioactive compounds, including drug candidates targeting central nervous system disorders and metabolic diseases.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿53,110.00
inventory 100mg
10-20 days ฿159,320.00

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Tert-butyl 3-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiazol-2-yl)pyrrolidine-1-carboxylate
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Used in organic synthesis as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds for constructing complex molecules, particularly in pharmaceutical and agrochemical research. The boronate ester group facilitates coupling with aryl or heteroaryl halides under palladium catalysis, while the Boc-protected pyrrolidine allows for further functionalization of nitrogen-containing heterocycles. Its structure supports the development of bioactive compounds,

Used in organic synthesis as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds for constructing complex molecules, particularly in pharmaceutical and agrochemical research. The boronate ester group facilitates coupling with aryl or heteroaryl halides under palladium catalysis, while the Boc-protected pyrrolidine allows for further functionalization of nitrogen-containing heterocycles. Its structure supports the development of bioactive compounds, including drug candidates targeting central nervous system disorders and metabolic diseases.

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