(S)-2-Amino-2-(3-chloro-4-fluorophenyl)ethanol

95%

Reagent Code: #236976
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CAS Number 496856-52-1

science Other reagents with same CAS 496856-52-1

blur_circular Chemical Specifications

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

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the production of serotonin-norepinephrine reuptake inhibitors (SNRIs) for treating depression and anxiety disorders. Its stereochemistry enables selective biological activity, improving drug efficacy and reducing side effects. Also employed in the development of novel kinase inhibitors and other central nervous system (CNS)-targeted therapeutics. Widely utilized in asymmetric synthesis due to its stable chiral center and functional group compatibility.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,270.00
inventory 250mg
10-20 days ฿20,250.00
inventory 1g
10-20 days ฿50,500.00
(S)-2-Amino-2-(3-chloro-4-fluorophenyl)ethanol
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Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the production of serotonin-norepinephrine reuptake inhibitors (SNRIs) for treating depression and anxiety disorders. Its stereochemistry enables selective biological activity, improving drug efficacy and reducing side effects. Also employed in the development of novel kinase inhibitors and other central nervous system (CNS)-targeted therapeutics. Widely utilized in asymmetric synthesis due to its stable chiral c

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the production of serotonin-norepinephrine reuptake inhibitors (SNRIs) for treating depression and anxiety disorders. Its stereochemistry enables selective biological activity, improving drug efficacy and reducing side effects. Also employed in the development of novel kinase inhibitors and other central nervous system (CNS)-targeted therapeutics. Widely utilized in asymmetric synthesis due to its stable chiral center and functional group compatibility.

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