tert-Butyl 2-(5-bromo-1H-imidazol-2-yl)pyrrolidine-1-carboxylate

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Reagent Code: #41770
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CAS Number 1352718-88-7

science Other reagents with same CAS 1352718-88-7

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Weight 316.1942 g/mol
Formula C₁₂H₁₈BrN₃O₂
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MDL Number MFCD24467648
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description Product Description

This chemical is primarily utilized in organic synthesis as a key intermediate in the development of pharmaceutical compounds. Its structure, featuring both imidazole and pyrrolidine rings, makes it valuable for constructing biologically active molecules, particularly in drug discovery and medicinal chemistry. It is often employed in the synthesis of inhibitors or modulators targeting enzymes or receptors, especially in the field of oncology and neurology. The bromo group on the imidazole ring allows for further functionalization through cross-coupling reactions, enabling the creation of diverse derivatives for biological evaluation. Additionally, the tert-butyloxycarbonyl (Boc) protecting group enhances its stability during synthetic processes, making it a practical choice for multi-step organic transformations.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,745.00

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tert-Butyl 2-(5-bromo-1H-imidazol-2-yl)pyrrolidine-1-carboxylate
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This chemical is primarily utilized in organic synthesis as a key intermediate in the development of pharmaceutical compounds. Its structure, featuring both imidazole and pyrrolidine rings, makes it valuable for constructing biologically active molecules, particularly in drug discovery and medicinal chemistry. It is often employed in the synthesis of inhibitors or modulators targeting enzymes or receptors, especially in the field of oncology and neurology. The bromo group on the imidazole ring allows for

This chemical is primarily utilized in organic synthesis as a key intermediate in the development of pharmaceutical compounds. Its structure, featuring both imidazole and pyrrolidine rings, makes it valuable for constructing biologically active molecules, particularly in drug discovery and medicinal chemistry. It is often employed in the synthesis of inhibitors or modulators targeting enzymes or receptors, especially in the field of oncology and neurology. The bromo group on the imidazole ring allows for further functionalization through cross-coupling reactions, enabling the creation of diverse derivatives for biological evaluation. Additionally, the tert-butyloxycarbonyl (Boc) protecting group enhances its stability during synthetic processes, making it a practical choice for multi-step organic transformations.

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