(S)-tert-Butyl 2-(3-bromophenyl)pyrrolidine-1-carboxylate

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Reagent Code: #71118
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CAS Number 2061996-90-3

science Other reagents with same CAS 2061996-90-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 326.23 g/mol
Formula C₁₁H₂₂O₂
badge Registry Numbers
MDL Number MFCD30609559
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in the development of pharmaceuticals and bioactive compounds. Its structure, featuring a pyrrolidine ring and a bromophenyl group, makes it a valuable intermediate in the construction of complex molecules. It is often employed in asymmetric synthesis to create chiral compounds, which are essential in the production of drugs with specific stereochemical requirements. Additionally, it serves as a building block in the synthesis of ligands for catalysis and in the preparation of compounds for biological studies, such as enzyme inhibitors or receptor modulators. Its bromine atom also allows for further functionalization through cross-coupling reactions, expanding its utility in medicinal chemistry and material science.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,368.00
inventory 250mg
10-20 days ฿20,745.00

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(S)-tert-Butyl 2-(3-bromophenyl)pyrrolidine-1-carboxylate
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This chemical is primarily utilized in organic synthesis, particularly in the development of pharmaceuticals and bioactive compounds. Its structure, featuring a pyrrolidine ring and a bromophenyl group, makes it a valuable intermediate in the construction of complex molecules. It is often employed in asymmetric synthesis to create chiral compounds, which are essential in the production of drugs with specific stereochemical requirements. Additionally, it serves as a building block in the synthesis of liga

This chemical is primarily utilized in organic synthesis, particularly in the development of pharmaceuticals and bioactive compounds. Its structure, featuring a pyrrolidine ring and a bromophenyl group, makes it a valuable intermediate in the construction of complex molecules. It is often employed in asymmetric synthesis to create chiral compounds, which are essential in the production of drugs with specific stereochemical requirements. Additionally, it serves as a building block in the synthesis of ligands for catalysis and in the preparation of compounds for biological studies, such as enzyme inhibitors or receptor modulators. Its bromine atom also allows for further functionalization through cross-coupling reactions, expanding its utility in medicinal chemistry and material science.

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