(S)-3-Amino-3-(4-fluorophenyl)propan-1-ol hydrochloride

97%

Reagent Code: #236414
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CAS Number 1213160-13-4

science Other reagents with same CAS 1213160-13-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 205.659 g/mol
Formula C₉H₁₃ClFNO
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the production of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system (CNS) active compounds. Its fluorinated aromatic structure and stereochemistry make it valuable for enhancing drug potency and metabolic stability. Commonly employed in the development of antidepressants and anxiolytic drugs, where the (S)-enantiomer contributes to targeted receptor binding. Also utilized in research settings for asymmetric synthesis and medicinal chemistry optimization.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,480.00
inventory 250mg
10-20 days ฿13,870.00
inventory 1g
10-20 days ฿37,510.00
(S)-3-Amino-3-(4-fluorophenyl)propan-1-ol hydrochloride
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Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the production of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system (CNS) active compounds. Its fluorinated aromatic structure and stereochemistry make it valuable for enhancing drug potency and metabolic stability. Commonly employed in the development of antidepressants and anxiolytic drugs, where the (S)-enantiomer contributes to targeted receptor binding. Also utilized in researc

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the production of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system (CNS) active compounds. Its fluorinated aromatic structure and stereochemistry make it valuable for enhancing drug potency and metabolic stability. Commonly employed in the development of antidepressants and anxiolytic drugs, where the (S)-enantiomer contributes to targeted receptor binding. Also utilized in research settings for asymmetric synthesis and medicinal chemistry optimization.

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