tert-Butyl 3-amino-3-(hydroxymethyl)azetidine-1-carboxylate

95%

Reagent Code: #65101
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CAS Number 1262411-27-7

science Other reagents with same CAS 1262411-27-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 202.25 g/mol
Formula C₉H₁₈N₂O₃
badge Registry Numbers
MDL Number MFCD18375152
thermostat Physical Properties
Boiling Point 300.1±27.0 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, inert gas

description Product Description

This chemical is primarily utilized in the field of organic synthesis, particularly as a building block for the development of more complex molecules. Its structure, featuring both an amino group and a hydroxymethyl group on an azetidine ring, makes it a versatile intermediate in the synthesis of pharmaceuticals. It is often employed in the preparation of compounds with potential biological activity, such as enzyme inhibitors or receptor modulators. The tert-butyloxycarbonyl (Boc) protecting group on the nitrogen atom allows for selective deprotection during multi-step synthetic processes, enabling precise control over the reaction sequence. This compound is especially valuable in medicinal chemistry for the design and optimization of drug candidates targeting various diseases.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿16,200.00
inventory 50mg
10-20 days ฿7,722.00

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tert-Butyl 3-amino-3-(hydroxymethyl)azetidine-1-carboxylate
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This chemical is primarily utilized in the field of organic synthesis, particularly as a building block for the development of more complex molecules. Its structure, featuring both an amino group and a hydroxymethyl group on an azetidine ring, makes it a versatile intermediate in the synthesis of pharmaceuticals. It is often employed in the preparation of compounds with potential biological activity, such as enzyme inhibitors or receptor modulators. The tert-butyloxycarbonyl (Boc) protecting group on the

This chemical is primarily utilized in the field of organic synthesis, particularly as a building block for the development of more complex molecules. Its structure, featuring both an amino group and a hydroxymethyl group on an azetidine ring, makes it a versatile intermediate in the synthesis of pharmaceuticals. It is often employed in the preparation of compounds with potential biological activity, such as enzyme inhibitors or receptor modulators. The tert-butyloxycarbonyl (Boc) protecting group on the nitrogen atom allows for selective deprotection during multi-step synthetic processes, enabling precise control over the reaction sequence. This compound is especially valuable in medicinal chemistry for the design and optimization of drug candidates targeting various diseases.

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