Benzyl (4-aminobicyclo[2.1.1]hexan-1-yl)carbamate hydrochloride

98%

Reagent Code: #152805
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CAS Number 1354951-84-0

science Other reagents with same CAS 1354951-84-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 282.77 g/mol
Formula C₁₄H₁₉ClN₂O₂
badge Registry Numbers
MDL Number MFCD20441712
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

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 enhances metabolic stability and influences blood-brain barrier penetration, making it valuable in designing neuroactive agents. The protected amine group allows for selective modifications in multi-step synthesis, enabling the creation of novel compounds with potential antidepressant or cognitive-enhancing effects.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿8,250.00
inventory 50mg
10-20 days ฿13,410.00
inventory 100mg
10-20 days ฿21,100.00
inventory 250mg
10-20 days ฿36,020.00

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Benzyl (4-aminobicyclo[2.1.1]hexan-1-yl)carbamate hydrochloride
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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 enhances metabolic stability and influences blood-brain barrier penetration, making it valuable in designing neuroactive agents. The protected amine group allows for selective modifications in multi-step synthesis, enabling the creation of novel compounds with potential antidepressant or cognitive-enhancing effects.

Used as an intermediate in pharmaceutical synthesis, particularly in the development of bioactive molecules targeting central nervous system disorders. Its rigid bicyclic structure enhances metabolic stability and influences blood-brain barrier penetration, making it valuable in designing neuroactive agents. The protected amine group allows for selective modifications in multi-step synthesis, enabling the creation of novel compounds with potential antidepressant or cognitive-enhancing effects.

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