(S)-1-(4-Fluoronaphthalen-1-yl)ethan-1-amine hydrochloride

95%

Reagent Code: #233452
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CAS Number 2703745-41-7

science Other reagents with same CAS 2703745-41-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 225.69 g/mol
Formula C₁₂H₁₃ClFN
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MDL Number MFCD34187011
inventory_2 Storage & Handling
Storage Room temperature, light-proof, inert gas

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of CNS-active compounds. Its fluorinated aromatic structure enhances binding affinity to certain neurological receptors, making it valuable in the production of selective serotonin or dopamine modulators. Commonly employed in asymmetric synthesis due to the chiral amine functionality, enabling the preparation of enantiomerically pure drugs. Also utilized in medicinal chemistry research for structure-activity relationship (SAR) studies involving fluorinated analogs.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿18,340.00
inventory 250mg
10-20 days ฿27,520.00

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(S)-1-(4-Fluoronaphthalen-1-yl)ethan-1-amine hydrochloride
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Used as a chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of CNS-active compounds. Its fluorinated aromatic structure enhances binding affinity to certain neurological receptors, making it valuable in the production of selective serotonin or dopamine modulators. Commonly employed in asymmetric synthesis due to the chiral amine functionality, enabling the preparation of enantiomerically pure drugs. Also utilized in medicinal chemistry research for structure-a

Used as a chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of CNS-active compounds. Its fluorinated aromatic structure enhances binding affinity to certain neurological receptors, making it valuable in the production of selective serotonin or dopamine modulators. Commonly employed in asymmetric synthesis due to the chiral amine functionality, enabling the preparation of enantiomerically pure drugs. Also utilized in medicinal chemistry research for structure-activity relationship (SAR) studies involving fluorinated analogs.

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