cis-3-Boc-3,7-diazabicyclo[4.2.0]octane

95%

Reagent Code: #173549
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CAS Number 1250993-51-1

science Other reagents with same CAS 1250993-51-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 212.29 g/mol
Formula C₁₁H₂₀N₂O₂
badge Registry Numbers
MDL Number MFCD20134217
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its rigid bicyclic structure and protected amine functionality make it valuable for constructing complex nitrogen-containing heterocycles. Commonly employed in medicinal chemistry for scaffold diversification and optimization of drug candidates targeting neurological disorders and cancer. The Boc-protected amine allows for selective deprotection and further functionalization, enabling efficient coupling in multi-step syntheses.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿4,820.00
inventory 250mg
10-20 days ฿21,260.00

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cis-3-Boc-3,7-diazabicyclo[4.2.0]octane
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its rigid bicyclic structure and protected amine functionality make it valuable for constructing complex nitrogen-containing heterocycles. Commonly employed in medicinal chemistry for scaffold diversification and optimization of drug candidates targeting neurological disorders and cancer. The Boc-protected amine allows for selective deprotection and

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its rigid bicyclic structure and protected amine functionality make it valuable for constructing complex nitrogen-containing heterocycles. Commonly employed in medicinal chemistry for scaffold diversification and optimization of drug candidates targeting neurological disorders and cancer. The Boc-protected amine allows for selective deprotection and further functionalization, enabling efficient coupling in multi-step syntheses.

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