endo-Bicyclo[2.2.1]heptan-2-amine hydrochloride

95%

Reagent Code: #150006
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CAS Number 65481-69-8

science Other reagents with same CAS 65481-69-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 147.65 g/mol
Formula C₇H₁₄ClN
badge Registry Numbers
MDL Number MFCD13193751
thermostat Physical Properties
Boiling Point 203.4 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, inert gas storage

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 norbornane structure provides stereochemical control in asymmetric synthesis, making it valuable in the preparation of enantiomerically pure drugs. Commonly employed in the production of antiviral, anticonvulsant, and neurodegenerative disease therapeutics. Also utilized in agrochemicals for creating bioactive molecules with enhanced selectivity. Serves as a catalyst precursor or ligand scaffold in organocatalysis and transition metal catalysis due to its amine functionality and defined spatial orientation.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿11,920.00
inventory 1g
10-20 days ฿32,160.00
inventory 5g
10-20 days ฿80,400.00

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endo-Bicyclo[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 norbornane structure provides stereochemical control in asymmetric synthesis, making it valuable in the preparation of enantiomerically pure drugs. Commonly employed in the production of antiviral, anticonvulsant, and neurodegenerative disease therapeutics. Also utilized in agrochemicals for creating bioactive molecules with enhanced selectivity. Serves as a cat

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. Its rigid norbornane structure provides stereochemical control in asymmetric synthesis, making it valuable in the preparation of enantiomerically pure drugs. Commonly employed in the production of antiviral, anticonvulsant, and neurodegenerative disease therapeutics. Also utilized in agrochemicals for creating bioactive molecules with enhanced selectivity. Serves as a catalyst precursor or ligand scaffold in organocatalysis and transition metal catalysis due to its amine functionality and defined spatial orientation.

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