tert-Butyl1,5-diazocane-1-carboxylate

98%

Reagent Code: #155348
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CAS Number 223797-64-6

science Other reagents with same CAS 223797-64-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.30 g/mol
Formula C₁₁H₂₂N₂O₂
badge Registry Numbers
MDL Number MFCD11616045
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a protected intermediate in organic synthesis, particularly in the preparation of nitrogen-containing heterocycles and pharmaceuticals. The tert-butyl carbamate (Boc) group provides stability during reactions and can be easily removed under mild acidic conditions, making it ideal for multi-step syntheses. It is commonly employed in the development of bioactive molecules, including enzyme inhibitors and receptor ligands, where controlled amine reactivity is required. Its eight-membered diazocane ring offers conformational flexibility, useful in medicinal chemistry for optimizing molecular binding and pharmacokinetic properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿19,500.00
inventory 250mg
10-20 days ฿32,830.00
tert-Butyl1,5-diazocane-1-carboxylate
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Used as a protected intermediate in organic synthesis, particularly in the preparation of nitrogen-containing heterocycles and pharmaceuticals. The tert-butyl carbamate (Boc) group provides stability during reactions and can be easily removed under mild acidic conditions, making it ideal for multi-step syntheses. It is commonly employed in the development of bioactive molecules, including enzyme inhibitors and receptor ligands, where controlled amine reactivity is required. Its eight-membered diazocane r

Used as a protected intermediate in organic synthesis, particularly in the preparation of nitrogen-containing heterocycles and pharmaceuticals. The tert-butyl carbamate (Boc) group provides stability during reactions and can be easily removed under mild acidic conditions, making it ideal for multi-step syntheses. It is commonly employed in the development of bioactive molecules, including enzyme inhibitors and receptor ligands, where controlled amine reactivity is required. Its eight-membered diazocane ring offers conformational flexibility, useful in medicinal chemistry for optimizing molecular binding and pharmacokinetic properties.

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