N-BOC-3-CARBETHOXY-4-PIPERIDONE

95%

Reagent Code: #216845
label
Alias 1-N-tert-butoxycarbonyl-4-oxo-3-piperidincarboxylate ethyl ester; N-BOC-4-oxo-3-piperidincarboxylate ethyl ester (P4); N-BOC-4-oxopiperidin-3-carboxylate ethyl ester; N-BOC-4-oxo-3-piperidincarboxylate ethyl ester; N-BOC-4-oxo-3-piperidincarboxylate ethyl ester; N-BOC-4-piperidincarboxylate ethyl ester; N-BOC-3-ethoxycarbonyl-4-piperidincarboxylate
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CAS Number 98977-34-5

science Other reagents with same CAS 98977-34-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 271.31 g/mol
Formula C₁₃H₂₁NO₅
badge Registry Numbers
MDL Number MFCD01862189
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 opioid antagonists and analgesics. Its protected amine group and functionalized piperidine ring make it valuable for constructing complex nitrogen-containing molecules. Commonly employed in multi-step organic syntheses where selective reactivity is required, especially in the preparation of substituted piperidines found in bioactive compounds. The BOC-protected amine allows for controlled deprotection and further derivatization, while the carbethoxy and ketone groups provide sites for nucleophilic attack or reduction, enabling diverse molecular transformations.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿174.00
inventory 5g
10-20 days ฿480.00
inventory 25g
10-20 days ฿1,880.00
inventory 100g
10-20 days ฿7,490.00
inventory 500g
10-20 days ฿36,690.00
N-BOC-3-CARBETHOXY-4-PIPERIDONE
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of opioid antagonists and analgesics. Its protected amine group and functionalized piperidine ring make it valuable for constructing complex nitrogen-containing molecules. Commonly employed in multi-step organic syntheses where selective reactivity is required, especially in the preparation of substituted piperidines found in bioactive compounds. The BOC-protected amine allows for controlled deprotection and furt
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of opioid antagonists and analgesics. Its protected amine group and functionalized piperidine ring make it valuable for constructing complex nitrogen-containing molecules. Commonly employed in multi-step organic syntheses where selective reactivity is required, especially in the preparation of substituted piperidines found in bioactive compounds. The BOC-protected amine allows for controlled deprotection and further derivatization, while the carbethoxy and ketone groups provide sites for nucleophilic attack or reduction, enabling diverse molecular transformations.
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