(1R,2R)-2-Fluorocyclopropanamine hydrochloride

98%

Reagent Code: #231255
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CAS Number 143062-85-5

science Other reagents with same CAS 143062-85-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 111.55 g/mol
Formula C₃H₇ClFN
badge Registry Numbers
MDL Number MFCD19205556
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a key chiral building block in the synthesis of pharmaceuticals, particularly in the development of fluorinated analogs of biologically active molecules. Its strained cyclopropane ring and fluorine substituent enhance metabolic stability and binding affinity in drug candidates. Commonly employed in the preparation of enzyme inhibitors and central nervous system agents. The amine functionality allows for coupling reactions, enabling incorporation into larger molecular structures. Valued in medicinal chemistry for structure-activity relationship studies due to its stereochemical purity and conformational rigidity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿9,570.00
1g
10-20 days ฿26,700.00
250mg
10-20 days ฿10,370.00
(1R,2R)-2-Fluorocyclopropanamine hydrochloride
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Used as a key chiral building block in the synthesis of pharmaceuticals, particularly in the development of fluorinated analogs of biologically active molecules. Its strained cyclopropane ring and fluorine substituent enhance metabolic stability and binding affinity in drug candidates. Commonly employed in the preparation of enzyme inhibitors and central nervous system agents. The amine functionality allows for coupling reactions, enabling incorporation into larger molecular structures. Valued in medicinal
Used as a key chiral building block in the synthesis of pharmaceuticals, particularly in the development of fluorinated analogs of biologically active molecules. Its strained cyclopropane ring and fluorine substituent enhance metabolic stability and binding affinity in drug candidates. Commonly employed in the preparation of enzyme inhibitors and central nervous system agents. The amine functionality allows for coupling reactions, enabling incorporation into larger molecular structures. Valued in medicinal chemistry for structure-activity relationship studies due to its stereochemical purity and conformational rigidity.
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