(tert-butoxy)-N-(trans-4-[(phenylmethoxy)carbonylamino]cyclohexylmethyl)carboxamide

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Reagent Code: #218869
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CAS Number 192323-61-8

science Other reagents with same CAS 192323-61-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 362.46 g/mol
Formula C₂₀H₃₀N₂O₄
badge Registry Numbers
MDL Number MFCD25977302
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a protecting group reagent in peptide synthesis, particularly for the selective protection of amino groups in complex organic transformations. Its tert-butoxy carbamate structure provides stability under various reaction conditions while allowing for clean deprotection under mild acidic conditions. Commonly employed in the preparation of intermediates for pharmaceuticals, especially in the development of protease inhibitors and other bioactive molecules. Its cyclohexyl and benzyl moieties enhance solubility and compatibility in organic solvents, making it suitable for solid-phase and solution-phase synthesis. Valued for high purity and minimal side reactions during coupling steps.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿30,270.00
(tert-butoxy)-N-(trans-4-[(phenylmethoxy)carbonylamino]cyclohexylmethyl)carboxamide
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Used as a protecting group reagent in peptide synthesis, particularly for the selective protection of amino groups in complex organic transformations. Its tert-butoxy carbamate structure provides stability under various reaction conditions while allowing for clean deprotection under mild acidic conditions. Commonly employed in the preparation of intermediates for pharmaceuticals, especially in the development of protease inhibitors and other bioactive molecules. Its cyclohexyl and benzyl moieties enhance

Used as a protecting group reagent in peptide synthesis, particularly for the selective protection of amino groups in complex organic transformations. Its tert-butoxy carbamate structure provides stability under various reaction conditions while allowing for clean deprotection under mild acidic conditions. Commonly employed in the preparation of intermediates for pharmaceuticals, especially in the development of protease inhibitors and other bioactive molecules. Its cyclohexyl and benzyl moieties enhance solubility and compatibility in organic solvents, making it suitable for solid-phase and solution-phase synthesis. Valued for high purity and minimal side reactions during coupling steps.

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