Dicyclohexylamine (S)-2-((tert-butoxycarbonyl)amino)non-8-enoate

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Reagent Code: #104361
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CAS Number 1058705-94-4

science Other reagents with same CAS 1058705-94-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 452.670 g/mol
Formula C₂₆H₄₈N₂O₄
badge Registry Numbers
MDL Number MFCD32196606
inventory_2 Storage & Handling
Storage 2-8°C, inert gas

description Product Description

Used in the synthesis of peptides and peptidomimetics, this compound serves as a key intermediate in organic chemistry. It is particularly valuable in the preparation of protected amino acid derivatives, which are essential for constructing complex peptide structures. The tert-butoxycarbonyl (Boc) group provides protection for the amine functionality during synthetic processes, ensuring selective reactions at other sites. Its application extends to the development of pharmaceuticals, where it aids in the creation of bioactive molecules with potential therapeutic effects. Additionally, it is utilized in research for studying enzyme mechanisms and protein interactions, contributing to advancements in biochemistry and drug discovery.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿20,160.00
inventory 250mg
10-20 days ฿7,470.00
inventory 100mg
10-20 days ฿4,401.00
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Dicyclohexylamine (S)-2-((tert-butoxycarbonyl)amino)non-8-enoate
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Used in the synthesis of peptides and peptidomimetics, this compound serves as a key intermediate in organic chemistry. It is particularly valuable in the preparation of protected amino acid derivatives, which are essential for constructing complex peptide structures. The tert-butoxycarbonyl (Boc) group provides protection for the amine functionality during synthetic processes, ensuring selective reactions at other sites. Its application extends to the development of pharmaceuticals, where it aids in the

Used in the synthesis of peptides and peptidomimetics, this compound serves as a key intermediate in organic chemistry. It is particularly valuable in the preparation of protected amino acid derivatives, which are essential for constructing complex peptide structures. The tert-butoxycarbonyl (Boc) group provides protection for the amine functionality during synthetic processes, ensuring selective reactions at other sites. Its application extends to the development of pharmaceuticals, where it aids in the creation of bioactive molecules with potential therapeutic effects. Additionally, it is utilized in research for studying enzyme mechanisms and protein interactions, contributing to advancements in biochemistry and drug discovery.

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