tert-Butyl ((3-azabicyclo[3.1.0]hexan-6-yl)methyl)(methyl)carbamate

95%

Reagent Code: #131207
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CAS Number 1781667-67-1

science Other reagents with same CAS 1781667-67-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 226.32 g/mol
Formula C₁₂H₂₂N₂O₂
badge Registry Numbers
MDL Number MFCD28634726
thermostat Physical Properties
Boiling Point 303.6±11.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.055±0.06 g/cm3(Predicted)
Storage 2-8°C, away from light, dry

description Product Description

Used as an intermediate in pharmaceutical synthesis, particularly in the development of bioactive molecules targeting central nervous system disorders. Its rigid bicyclic structure and protected amine functionality make it valuable for constructing peptidomimetics and small-molecule therapeutics with enhanced metabolic stability and selectivity. Commonly employed in medicinal chemistry campaigns to optimize lead compounds, especially in projects involving receptor modulation or enzyme inhibition. The tert-butyl carbamate group allows for selective deprotection under mild acidic conditions, enabling stepwise assembly of complex amines. Also utilized in the synthesis of novel ligands for GPCRs and ion channels due to its favorable stereochemistry and conformational restraint.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿16,660.00
inventory 50mg
10-20 days ฿9,800.00

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tert-Butyl ((3-azabicyclo[3.1.0]hexan-6-yl)methyl)(methyl)carbamate
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Used as an intermediate in pharmaceutical synthesis, particularly in the development of bioactive molecules targeting central nervous system disorders. Its rigid bicyclic structure and protected amine functionality make it valuable for constructing peptidomimetics and small-molecule therapeutics with enhanced metabolic stability and selectivity. Commonly employed in medicinal chemistry campaigns to optimize lead compounds, especially in projects involving receptor modulation or enzyme inhibition. The ter

Used as an intermediate in pharmaceutical synthesis, particularly in the development of bioactive molecules targeting central nervous system disorders. Its rigid bicyclic structure and protected amine functionality make it valuable for constructing peptidomimetics and small-molecule therapeutics with enhanced metabolic stability and selectivity. Commonly employed in medicinal chemistry campaigns to optimize lead compounds, especially in projects involving receptor modulation or enzyme inhibition. The tert-butyl carbamate group allows for selective deprotection under mild acidic conditions, enabling stepwise assembly of complex amines. Also utilized in the synthesis of novel ligands for GPCRs and ion channels due to its favorable stereochemistry and conformational restraint.

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