tert-butyl [3,3'-biazetidine]-1-carboxylate hydrochloride

99%

Reagent Code: #238601
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CAS Number 2007910-70-3

science Other reagents with same CAS 2007910-70-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 248.7496 g/mol
Formula C₁₁H₂₁ClN₂O₂
badge Registry Numbers
MDL Number MFCD30471683
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules requiring constrained nitrogen-containing scaffolds. Its biazetidine core provides structural rigidity, enhancing selectivity and metabolic stability in drug candidates. The tert-butyl carbamate (Boc) protection allows for controlled deprotection in multi-step syntheses, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in the preparation of kinase inhibitors and central nervous system agents.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿16,080.00
inventory 250mg
10-20 days ฿32,310.00
inventory 1g
10-20 days ฿80,160.00
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tert-butyl [3,3'-biazetidine]-1-carboxylate hydrochloride
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules requiring constrained nitrogen-containing scaffolds. Its biazetidine core provides structural rigidity, enhancing selectivity and metabolic stability in drug candidates. The tert-butyl carbamate (Boc) protection allows for controlled deprotection in multi-step syntheses, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in the preparation

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules requiring constrained nitrogen-containing scaffolds. Its biazetidine core provides structural rigidity, enhancing selectivity and metabolic stability in drug candidates. The tert-butyl carbamate (Boc) protection allows for controlled deprotection in multi-step syntheses, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in the preparation of kinase inhibitors and central nervous system agents.

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