1-Boc-azetidine-3-ylmethanol

97%

Reagent Code: #143735
label
Alias 1-Tert-butoxycarbonyl-3-hydroxymethylazetidane; 1-BOC-azetidane-3-ylmethanol; 3-hydroxymethyl-azetidane-1-carboxylate tert-butyl ester; N-BOC-3-hydroxymethylazetidane; 1-BOC-3-hydroxymethylazetidane; 1-BOC-3-hydroxymethylazetidane; 1-BOC-3-azetidane methanol
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CAS Number 142253-56-3

science Other reagents with same CAS 142253-56-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 187.24 g/mol
Formula C₉H₁₇NO₃
badge Registry Numbers
MDL Number MFCD06656141
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) where the azetidine ring serves as a structural motif to enhance metabolic stability and bioavailability. The Boc-protected amine functionality allows for selective deprotection, while the free alcohol group enables further derivatization, making it valuable in multi-step organic synthesis, especially in drug discovery programs targeting CNS disorders, antiviral agents, and kinase inhibitors. Its compact ring structure is often employed to improve potency and reduce off-target effects in medicinal chemistry campaigns.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿159.50
inventory 1g
10-20 days ฿350.00
inventory 25g
10-20 days ฿3,310.00
inventory 100g
10-20 days ฿12,510.00
inventory 5g
10-20 days ฿720.00

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1-Boc-azetidine-3-ylmethanol
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) where the azetidine ring serves as a structural motif to enhance metabolic stability and bioavailability. The Boc-protected amine functionality allows for selective deprotection, while the free alcohol group enables further derivatization, making it valuable in multi-step organic synthesis, especially in drug discovery programs targeting CNS disorders, antiv

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) where the azetidine ring serves as a structural motif to enhance metabolic stability and bioavailability. The Boc-protected amine functionality allows for selective deprotection, while the free alcohol group enables further derivatization, making it valuable in multi-step organic synthesis, especially in drug discovery programs targeting CNS disorders, antiviral agents, and kinase inhibitors. Its compact ring structure is often employed to improve potency and reduce off-target effects in medicinal chemistry campaigns.

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