(S)-tert-Butyl 2-(5-(6-bromonaphthalen-2-yl)-1H-imidazol-2-yl)pyrrolidine-1-carboxylate

95%

Reagent Code: #38152
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CAS Number 1228551-96-9

science Other reagents with same CAS 1228551-96-9

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scatter_plot Molecular Information
Weight 442.3489 g/mol
Formula C₂₂H₂₄BrN₃O₂
badge Registry Numbers
MDL Number MFCD26392790
inventory_2 Storage & Handling
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description Product Description

This compound is primarily utilized in pharmaceutical research as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring a bromonaphthalene group and an imidazole ring, makes it valuable in the development of potential drug candidates targeting specific enzymes or receptors. It is often employed in the design of inhibitors for therapeutic applications, particularly in areas such as oncology and inflammation. The compound’s chiral center also allows for the exploration of stereoselective interactions in drug development, enhancing the precision of pharmacological studies. Researchers leverage its unique properties to optimize drug efficacy and selectivity in preclinical studies.

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inventory 250mg
10-20 days ฿5,688.00

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(S)-tert-Butyl 2-(5-(6-bromonaphthalen-2-yl)-1H-imidazol-2-yl)pyrrolidine-1-carboxylate
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This compound is primarily utilized in pharmaceutical research as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring a bromonaphthalene group and an imidazole ring, makes it valuable in the development of potential drug candidates targeting specific enzymes or receptors. It is often employed in the design of inhibitors for therapeutic applications, particularly in areas such as oncology and inflammation. The compound’s chiral center also allows for the explorat

This compound is primarily utilized in pharmaceutical research as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring a bromonaphthalene group and an imidazole ring, makes it valuable in the development of potential drug candidates targeting specific enzymes or receptors. It is often employed in the design of inhibitors for therapeutic applications, particularly in areas such as oncology and inflammation. The compound’s chiral center also allows for the exploration of stereoselective interactions in drug development, enhancing the precision of pharmacological studies. Researchers leverage its unique properties to optimize drug efficacy and selectivity in preclinical studies.

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