tert-Butyl (2S)-2-[5-(4-bromophenyl)-1H-imidazol-2-yl]pyrrolidine-1-carboxylate

95%

Reagent Code: #83011
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CAS Number 1007882-04-3

science Other reagents with same CAS 1007882-04-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 392.290 g/mol
Formula C₁₈H₂₂BrN₃O₂
badge Registry Numbers
MDL Number MFCD19982645
thermostat Physical Properties
Boiling Point 567.2±45.0 °C
inventory_2 Storage & Handling
Density 1.380±0.06 g/cm3
Storage 2-8°C, protected from light, dry

description Product Description

This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of biologically active molecules, particularly those targeting specific enzymes or receptors. Its structure, featuring an imidazole ring and a pyrrolidine moiety, makes it valuable for developing compounds with potential therapeutic applications, such as inhibitors for certain diseases or conditions. Researchers often employ it in the design and optimization of drug candidates, leveraging its functional groups to enhance binding affinity or selectivity. Additionally, it may be used in studies exploring structure-activity relationships (SAR) to identify more effective and targeted pharmaceutical agents.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿8,730.00
inventory 1g
10-20 days ฿25,920.00

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tert-Butyl (2S)-2-[5-(4-bromophenyl)-1H-imidazol-2-yl]pyrrolidine-1-carboxylate
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This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of biologically active molecules, particularly those targeting specific enzymes or receptors. Its structure, featuring an imidazole ring and a pyrrolidine moiety, makes it valuable for developing compounds with potential therapeutic applications, such as inhibitors for certain diseases or conditions. Researchers often employ it in the design and optimization of drug candidates, leveraging its functional groups to enhance binding affinity or selectivity. Additionally, it may be used in studies exploring structure-activity relationships (SAR) to identify more effective and targeted pharmaceutical agents.
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