benzyl4-aminobicyclo[2.1.1]hexan-1-ylcarbamate

98%

Reagent Code: #155036
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CAS Number 1355004-67-9

science Other reagents with same CAS 1355004-67-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 246.3 g/mol
Formula C₁₄H₁₈N₂O₂
badge Registry Numbers
MDL Number MFCD25458139
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as an intermediate in pharmaceutical synthesis, particularly in the development of neuroactive compounds. Its rigid bicyclic structure enhances binding selectivity to central nervous system targets, making it valuable in designing drugs for neurological disorders. Commonly employed in prodrug strategies due to the benzyl carbamate group, which can improve blood-brain barrier penetration and metabolic stability. Also utilized in medicinal chemistry research to explore structure-activity relationships in receptor modulators.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿23,680.00
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benzyl4-aminobicyclo[2.1.1]hexan-1-ylcarbamate
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Used as an intermediate in pharmaceutical synthesis, particularly in the development of neuroactive compounds. Its rigid bicyclic structure enhances binding selectivity to central nervous system targets, making it valuable in designing drugs for neurological disorders. Commonly employed in prodrug strategies due to the benzyl carbamate group, which can improve blood-brain barrier penetration and metabolic stability. Also utilized in medicinal chemistry research to explore structure-activity relationships

Used as an intermediate in pharmaceutical synthesis, particularly in the development of neuroactive compounds. Its rigid bicyclic structure enhances binding selectivity to central nervous system targets, making it valuable in designing drugs for neurological disorders. Commonly employed in prodrug strategies due to the benzyl carbamate group, which can improve blood-brain barrier penetration and metabolic stability. Also utilized in medicinal chemistry research to explore structure-activity relationships in receptor modulators.

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