(S)-2-(tert-Butoxycarbonyl)isoxazolidine-3-carboxylic Acid

98%

Reagent Code: #235304
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CAS Number 1372202-46-4

science Other reagents with same CAS 1372202-46-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.22 g/mol
Formula C₉H₁₅NO₅
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of β-amino acid derivatives and peptidomimetics. Its protected isoxazolidine ring serves as a scaffold for constructing complex molecules with defined stereochemistry. Commonly employed in medicinal chemistry for the preparation of enzyme inhibitors and bioactive compounds where stereocontrol is critical. The Boc-protected amine allows for selective deprotection and further functionalization in multi-step organic syntheses.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿4,950.00
(S)-2-(tert-Butoxycarbonyl)isoxazolidine-3-carboxylic Acid
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of β-amino acid derivatives and peptidomimetics. Its protected isoxazolidine ring serves as a scaffold for constructing complex molecules with defined stereochemistry. Commonly employed in medicinal chemistry for the preparation of enzyme inhibitors and bioactive compounds where stereocontrol is critical. The Boc-protected amine allows for selective deprotection and further functionalization in multi-step

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of β-amino acid derivatives and peptidomimetics. Its protected isoxazolidine ring serves as a scaffold for constructing complex molecules with defined stereochemistry. Commonly employed in medicinal chemistry for the preparation of enzyme inhibitors and bioactive compounds where stereocontrol is critical. The Boc-protected amine allows for selective deprotection and further functionalization in multi-step organic syntheses.

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