N-Methylbicyclo[2.2.1]heptan-2-amine hydrochloride

95%

Reagent Code: #215592
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CAS Number 90203-82-0

science Other reagents with same CAS 90203-82-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 161.67 g/mol
Formula C₈H₁₆ClN
badge Registry Numbers
MDL Number MFCD28118423
thermostat Physical Properties
Melting Point 193-194 °C
inventory_2 Storage & Handling
Storage Room temperature, seal, inert gas

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. Its rigid bicyclic structure and defined stereochemistry make it valuable for designing bioactive molecules with high selectivity. Commonly employed in medicinal chemistry for structure-activity relationship studies, especially in optimizing receptor binding and metabolic stability. Also utilized in asymmetric synthesis as a scaffold or auxiliary due to its amine functionality, which can be readily modified for coupling reactions.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿4,580.00
250mg
10-20 days ฿8,420.00
N-Methylbicyclo[2.2.1]heptan-2-amine hydrochloride
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. Its rigid bicyclic structure and defined stereochemistry make it valuable for designing bioactive molecules with high selectivity. Commonly employed in medicinal chemistry for structure-activity relationship studies, especially in optimizing receptor binding and metabolic stability. Also utilized in asymmetric synthesis as a scaffold or auxiliary due to its amine function

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. Its rigid bicyclic structure and defined stereochemistry make it valuable for designing bioactive molecules with high selectivity. Commonly employed in medicinal chemistry for structure-activity relationship studies, especially in optimizing receptor binding and metabolic stability. Also utilized in asymmetric synthesis as a scaffold or auxiliary due to its amine functionality, which can be readily modified for coupling reactions.

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