(1R,3R)-3-(((Benzyloxy)carbonyl)amino)cyclohexyl acetate

95%

Reagent Code: #87026
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CAS Number 750649-42-4

science Other reagents with same CAS 750649-42-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 291.34 g/mol
Formula C₁₆H₂₁NO₄
badge Registry Numbers
MDL Number MFCD30472098
inventory_2 Storage & Handling
Storage 2-8°C, dry, airtight

description Product Description

This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs) for therapeutic drugs. Its structure, featuring a benzyloxycarbonyl-protected amine and an acetate group, makes it a valuable building block in organic synthesis. It is often employed in the preparation of cyclohexane-based compounds, which are key components in drugs targeting neurological and inflammatory conditions. Additionally, it serves as a precursor in the production of chiral molecules, enabling the creation of enantiomerically pure substances critical for drug efficacy and safety. Its role in peptide synthesis is also notable, as it aids in the protection and deprotection of amino groups during the formation of complex peptide chains.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,825.00

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(1R,3R)-3-(((Benzyloxy)carbonyl)amino)cyclohexyl acetate
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This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs) for therapeutic drugs. Its structure, featuring a benzyloxycarbonyl-protected amine and an acetate group, makes it a valuable building block in organic synthesis. It is often employed in the preparation of cyclohexane-based compounds, which are key components in drugs targeting neurological and inflammatory conditions. Additionally, it serves as

This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs) for therapeutic drugs. Its structure, featuring a benzyloxycarbonyl-protected amine and an acetate group, makes it a valuable building block in organic synthesis. It is often employed in the preparation of cyclohexane-based compounds, which are key components in drugs targeting neurological and inflammatory conditions. Additionally, it serves as a precursor in the production of chiral molecules, enabling the creation of enantiomerically pure substances critical for drug efficacy and safety. Its role in peptide synthesis is also notable, as it aids in the protection and deprotection of amino groups during the formation of complex peptide chains.

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