((2S,7aR)-2-Fluorotetrahydro-1H-pyrrolizin-7a(5H)-yl)methanol

98%

Reagent Code: #236894
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CAS Number 2621939-48-6

science Other reagents with same CAS 2621939-48-6

blur_circular Chemical Specifications

inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used in pharmaceutical synthesis as a chiral building block for developing neuroactive compounds. Its fluorinated pyrrolizine structure enhances metabolic stability and blood-brain barrier penetration, making it valuable in the design of central nervous system agents. Commonly employed in the preparation of experimental treatments for neurological disorders such as epilepsy, depression, and neuropathic pain. Also utilized in structure-activity relationship studies to optimize potency and selectivity of new drug candidates.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25mg
10-20 days ฿8,510.00
100mg
10-20 days ฿17,520.00
250mg
10-20 days ฿29,190.00
1g
10-20 days ฿63,230.00
50mg
10-20 days ฿14,610.00
((2S,7aR)-2-Fluorotetrahydro-1H-pyrrolizin-7a(5H)-yl)methanol
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Used in pharmaceutical synthesis as a chiral building block for developing neuroactive compounds. Its fluorinated pyrrolizine structure enhances metabolic stability and blood-brain barrier penetration, making it valuable in the design of central nervous system agents. Commonly employed in the preparation of experimental treatments for neurological disorders such as epilepsy, depression, and neuropathic pain. Also utilized in structure-activity relationship studies to optimize potency and selectivity of new
Used in pharmaceutical synthesis as a chiral building block for developing neuroactive compounds. Its fluorinated pyrrolizine structure enhances metabolic stability and blood-brain barrier penetration, making it valuable in the design of central nervous system agents. Commonly employed in the preparation of experimental treatments for neurological disorders such as epilepsy, depression, and neuropathic pain. Also utilized in structure-activity relationship studies to optimize potency and selectivity of new drug candidates.
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