(S)-tert-butyl(1-(4-phenyl-1H-imidazol-2-yl)ethyl)carbamate

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Reagent Code: #237661
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CAS Number 1993394-53-8

science Other reagents with same CAS 1993394-53-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 287.36 g/mol
Formula C₁₆H₂₁N₃O₂
badge Registry Numbers
MDL Number MFCD29472362
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of imidazole-based bioactive molecules. Its protected amine group allows for selective reactions in multi-step organic syntheses. Commonly employed in the preparation of protease inhibitors and receptor antagonists due to the stability and stereochemical purity it provides. The tert-butyl carbamate (Boc) protection enables mild deprotection conditions, making it suitable for sensitive drug intermediates. Widely applied in medicinal chemistry for optimizing pharmacokinetic properties and enhancing enantioselectivity in final drug candidates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿54,080.00
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(S)-tert-butyl(1-(4-phenyl-1H-imidazol-2-yl)ethyl)carbamate
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Used as a chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of imidazole-based bioactive molecules. Its protected amine group allows for selective reactions in multi-step organic syntheses. Commonly employed in the preparation of protease inhibitors and receptor antagonists due to the stability and stereochemical purity it provides. The tert-butyl carbamate (Boc) protection enables mild deprotection conditions, making it suitable for sensitive drug intermed

Used as a chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of imidazole-based bioactive molecules. Its protected amine group allows for selective reactions in multi-step organic syntheses. Commonly employed in the preparation of protease inhibitors and receptor antagonists due to the stability and stereochemical purity it provides. The tert-butyl carbamate (Boc) protection enables mild deprotection conditions, making it suitable for sensitive drug intermediates. Widely applied in medicinal chemistry for optimizing pharmacokinetic properties and enhancing enantioselectivity in final drug candidates.

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