Ethyl 1-((tert-butoxycarbonyl)amino)cyclopropanecarboxylate

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Reagent Code: #182712
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CAS Number 107259-05-2

science Other reagents with same CAS 107259-05-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 229.27 g/mol
Formula C₁₁H₁₉NO₄
badge Registry Numbers
MDL Number MFCD11845623
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals. Its structure contains both a protected amine (Boc group) and an ester functionality, making it valuable in peptide synthesis and the construction of complex molecules. The cyclopropane ring introduces conformational rigidity, which is often exploited in drug design to enhance metabolic stability and receptor selectivity. Commonly employed in the development of protease inhibitors and other therapeutic agents where precise stereochemistry and steric constraints are important.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿670.00
inventory 1g
10-20 days ฿1,590.00
inventory 5g
10-20 days ฿5,710.00
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Ethyl 1-((tert-butoxycarbonyl)amino)cyclopropanecarboxylate
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Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals. Its structure contains both a protected amine (Boc group) and an ester functionality, making it valuable in peptide synthesis and the construction of complex molecules. The cyclopropane ring introduces conformational rigidity, which is often exploited in drug design to enhance metabolic stability and receptor selectivity. Commonly employed in the development of protease inhibitors and other ther

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals. Its structure contains both a protected amine (Boc group) and an ester functionality, making it valuable in peptide synthesis and the construction of complex molecules. The cyclopropane ring introduces conformational rigidity, which is often exploited in drug design to enhance metabolic stability and receptor selectivity. Commonly employed in the development of protease inhibitors and other therapeutic agents where precise stereochemistry and steric constraints are important.

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