1-Boc-3-cyano-4-pyrrolidinone

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Reagent Code: #143481
label
Alias 1-Boc-3-cyano-4-pyrrolidone
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CAS Number 175463-32-8

science Other reagents with same CAS 175463-32-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 210.23 g/mol
Formula C₁₀H₁₄N₂O₃
badge Registry Numbers
MDL Number MFCD01318456
thermostat Physical Properties
Melting Point 160-167°C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex nitrogen-containing heterocycles. The Boc-protected amine and cyano group enable sequential deprotection and transformation steps, facilitating efficient multi-step syntheses. Commonly employed in research settings for drug discovery programs targeting cancer, inflammation, and central nervous system disorders.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿162.00
inventory 1g
10-20 days ฿320.00
inventory 5g
10-20 days ฿600.00
inventory 25g
10-20 days ฿2,880.00

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1-Boc-3-cyano-4-pyrrolidinone
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex nitrogen-containing heterocycles. The Boc-protected amine and cyano group enable sequential deprotection and transformation steps, facilitating efficient multi-step syntheses. Commonly employed in research settings for drug discov

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex nitrogen-containing heterocycles. The Boc-protected amine and cyano group enable sequential deprotection and transformation steps, facilitating efficient multi-step syntheses. Commonly employed in research settings for drug discovery programs targeting cancer, inflammation, and central nervous system disorders.

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