Dicyclohexylamine (R)-2-((tert-butoxycarbonyl)amino)-3-(furan-2-yl)propanoate

95%

Reagent Code: #177567
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CAS Number 331730-09-7

science Other reagents with same CAS 331730-09-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 436.585 g/mol
Formula C₂₄H₄₀N₂O₅
badge Registry Numbers
MDL Number MFCD01860889
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other bioactive molecules. Its structure supports chiral synthesis, making it valuable in asymmetric reactions for producing enantiomerically pure drugs. Commonly employed in peptide chemistry due to the Boc-protected amino group, allowing selective deprotection and coupling steps. The furan ring can act as a versatile handle for further functionalization or as a pharmacophore in medicinal chemistry. Stable under a variety of reaction conditions, it is suitable for multi-step organic syntheses in drug discovery and process development.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,280.00
inventory 250mg
10-20 days ฿7,910.00
inventory 1g
10-20 days ฿24,140.00

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Dicyclohexylamine (R)-2-((tert-butoxycarbonyl)amino)-3-(furan-2-yl)propanoate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other bioactive molecules. Its structure supports chiral synthesis, making it valuable in asymmetric reactions for producing enantiomerically pure drugs. Commonly employed in peptide chemistry due to the Boc-protected amino group, allowing selective deprotection and coupling steps. The furan ring can act as a versatile handle for further functionalization or as a pharmacophore in medicinal chemistry. Stable under a variety of reaction conditions, it is suitable for multi-step organic syntheses in drug discovery and process development.
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