trans-Methyl 3-((tert-butoxycarbonyl)amino)cyclobutanecarboxylate

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Reagent Code: #209477
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CAS Number 1101173-77-6

science Other reagents with same CAS 1101173-77-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 229.27 g/mol
Formula C₁₁H₁₉NO₄
badge Registry Numbers
MDL Number MFCD20922912
thermostat Physical Properties
Boiling Point 314.1±31.0 °C
inventory_2 Storage & Handling
Density 1.10±0.1 g/cm3
Storage 2-8°C, dry

description Product Description

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical development. Its protected amine and ester functional groups make it valuable for constructing peptidomimetics and cyclic amino acid derivatives. Commonly employed in medicinal chemistry for designing enzyme inhibitors and receptor modulators, especially where conformational restriction is needed. The tert-butoxycarbonyl (Boc) group allows for selective deprotection under mild acidic conditions, enabling stepwise assembly of complex molecules. The trans configuration supports defined stereochemistry in final products, important for optimizing potency and selectivity in drug candidates.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,370.00
inventory 5g
10-20 days ฿11,190.00
inventory 10g
10-20 days ฿20,210.00

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trans-Methyl 3-((tert-butoxycarbonyl)amino)cyclobutanecarboxylate
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Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical development. Its protected amine and ester functional groups make it valuable for constructing peptidomimetics and cyclic amino acid derivatives. Commonly employed in medicinal chemistry for designing enzyme inhibitors and receptor modulators, especially where conformational restriction is needed. The tert-butoxycarbonyl (Boc) group allows for selective deprotection under mild acidic conditions, e

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical development. Its protected amine and ester functional groups make it valuable for constructing peptidomimetics and cyclic amino acid derivatives. Commonly employed in medicinal chemistry for designing enzyme inhibitors and receptor modulators, especially where conformational restriction is needed. The tert-butoxycarbonyl (Boc) group allows for selective deprotection under mild acidic conditions, enabling stepwise assembly of complex molecules. The trans configuration supports defined stereochemistry in final products, important for optimizing potency and selectivity in drug candidates.

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