Dicyclohexylamine(S)-2-((tert-butoxycarbonyl)amino)-5-phenylpentanoate

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Reagent Code: #177522
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CAS Number 113756-89-1

science Other reagents with same CAS 113756-89-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 474.68 g/mol
Formula C₂₈H₄₆N₂O₄
badge Registry Numbers
MDL Number MFCD06410979
inventory_2 Storage & Handling
Storage 2-8°C, inert atmosphere

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of chiral drugs where stereochemistry plays a critical role. Its structure supports the introduction of protected amino groups and hydrophobic moieties, making it valuable in peptide-like molecule construction. Commonly employed in organic synthesis for building blocks in protease inhibitors or receptor modulators. The Boc-protected amine allows for controlled deprotection and further functionalization in multi-step reactions. Its cyclohexyl and phenyl groups aid in crystallization and purification during drug development.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,130.00
inventory 250mg
10-20 days ฿3,170.00
inventory 1g
10-20 days ฿7,850.00

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Dicyclohexylamine(S)-2-((tert-butoxycarbonyl)amino)-5-phenylpentanoate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of chiral drugs where stereochemistry plays a critical role. Its structure supports the introduction of protected amino groups and hydrophobic moieties, making it valuable in peptide-like molecule construction. Commonly employed in organic synthesis for building blocks in protease inhibitors or receptor modulators. The Boc-protected amine allows for controlled deprotection and further functionalization i

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of chiral drugs where stereochemistry plays a critical role. Its structure supports the introduction of protected amino groups and hydrophobic moieties, making it valuable in peptide-like molecule construction. Commonly employed in organic synthesis for building blocks in protease inhibitors or receptor modulators. The Boc-protected amine allows for controlled deprotection and further functionalization in multi-step reactions. Its cyclohexyl and phenyl groups aid in crystallization and purification during drug development.

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