(S)-tert-Butyl (1-(1,3-dioxoisoindolin-2-yl)-3-(3-fluorophenyl)propan-2-yl)carbamate

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Reagent Code: #113611
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CAS Number 1201923-48-9

science Other reagents with same CAS 1201923-48-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 398.43 g/mol
Formula C₂₂H₂₃FN₂O₄
badge Registry Numbers
MDL Number MFCD28359281
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of biologically active molecules. Its structure, featuring a fluorophenyl group and a dioxoisoindoline moiety, makes it a valuable building block for developing potential pharmaceuticals, particularly in the design of enzyme inhibitors or receptor modulators. The presence of the tert-butyl carbamate group provides stability and facilitates further chemical modifications, enabling the creation of targeted drug candidates. Researchers often employ it in the development of compounds for treating neurological disorders or cancer, where selective interaction with biological targets is crucial. Its application is also seen in peptide chemistry, where it serves as a protective group during the synthesis of complex peptide structures.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,637.00
inventory 100mg
10-20 days ฿1,557.00

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(S)-tert-Butyl (1-(1,3-dioxoisoindolin-2-yl)-3-(3-fluorophenyl)propan-2-yl)carbamate
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This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of biologically active molecules. Its structure, featuring a fluorophenyl group and a dioxoisoindoline moiety, makes it a valuable building block for developing potential pharmaceuticals, particularly in the design of enzyme inhibitors or receptor modulators. The presence of the tert-butyl carbamate group provides stability and facilitates further chemical modifications, enabling the creation of targeted drug candidates. Researchers often employ it in the development of compounds for treating neurological disorders or cancer, where selective interaction with biological targets is crucial. Its application is also seen in peptide chemistry, where it serves as a protective group during the synthesis of complex peptide structures.
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