tert-Butyl 2-((tert-butoxycarbonyl)amino)-2-cyanoacetate

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Reagent Code: #148264
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CAS Number 130892-40-9

science Other reagents with same CAS 130892-40-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 256.30 g/mol
Formula C₁₂H₂₀N₂O₄
badge Registry Numbers
MDL Number MFCD24466150
thermostat Physical Properties
Boiling Point 370.0±32.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry seal

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of amino acid derivatives and peptide mimetics. Its cyano and ester functional groups allow for diverse transformations, including hydrolysis, reduction, and nucleophilic addition, enabling the construction of complex nitrogen-containing molecules. Commonly employed in medicinal chemistry for the synthesis of protected α-amino acids and heterocyclic compounds. The dual protection (Boc and tert-butyl ester) permits selective deprotection and stepwise elaboration in multi-step syntheses, making it valuable in the development of pharmaceuticals and bioactive molecules.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,010.00
inventory 250mg
10-20 days ฿2,190.00

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tert-Butyl 2-((tert-butoxycarbonyl)amino)-2-cyanoacetate
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Used as a key intermediate in organic synthesis, particularly in the preparation of amino acid derivatives and peptide mimetics. Its cyano and ester functional groups allow for diverse transformations, including hydrolysis, reduction, and nucleophilic addition, enabling the construction of complex nitrogen-containing molecules. Commonly employed in medicinal chemistry for the synthesis of protected α-amino acids and heterocyclic compounds. The dual protection (Boc and tert-butyl ester) permits selective

Used as a key intermediate in organic synthesis, particularly in the preparation of amino acid derivatives and peptide mimetics. Its cyano and ester functional groups allow for diverse transformations, including hydrolysis, reduction, and nucleophilic addition, enabling the construction of complex nitrogen-containing molecules. Commonly employed in medicinal chemistry for the synthesis of protected α-amino acids and heterocyclic compounds. The dual protection (Boc and tert-butyl ester) permits selective deprotection and stepwise elaboration in multi-step syntheses, making it valuable in the development of pharmaceuticals and bioactive molecules.

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