Ethyl 1-benzyl-4-(1-((tert-butoxycarbonyl)amino)cyclopropyl)pyrrolidine-3-carboxylate

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Reagent Code: #86558
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CAS Number 307976-20-1

science Other reagents with same CAS 307976-20-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 388.51 g/mol
Formula C₂₂H₃₂N₂O₄
badge Registry Numbers
MDL Number MFCD13191515
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research. It serves as a key intermediate in the development of biologically active compounds, including potential drug candidates. Its structure, featuring a pyrrolidine ring and cyclopropyl group, makes it valuable for constructing molecules with specific stereochemistry and functional groups. The tert-butoxycarbonyl (Boc) protecting group allows for selective reactions during synthesis, enabling the creation of targeted compounds. Its applications are often seen in the preparation of peptidomimetics or other therapeutic agents, where precise molecular architecture is crucial for biological activity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿37,800.00

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Ethyl 1-benzyl-4-(1-((tert-butoxycarbonyl)amino)cyclopropyl)pyrrolidine-3-carboxylate
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This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research. It serves as a key intermediate in the development of biologically active compounds, including potential drug candidates. Its structure, featuring a pyrrolidine ring and cyclopropyl group, makes it valuable for constructing molecules with specific stereochemistry and functional groups. The tert-butoxycarbonyl (Boc) protecting group allows for selective reactions during synthesis, en

This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research. It serves as a key intermediate in the development of biologically active compounds, including potential drug candidates. Its structure, featuring a pyrrolidine ring and cyclopropyl group, makes it valuable for constructing molecules with specific stereochemistry and functional groups. The tert-butoxycarbonyl (Boc) protecting group allows for selective reactions during synthesis, enabling the creation of targeted compounds. Its applications are often seen in the preparation of peptidomimetics or other therapeutic agents, where precise molecular architecture is crucial for biological activity.

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