2-Amino-2-(4-chloro-3-fluorophenyl)ethan-1-ol hydrochloride

95%

Reagent Code: #138144
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CAS Number 1427380-48-0

science Other reagents with same CAS 1427380-48-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 226.08 g/mol
Formula C₈H₁₀Cl₂FNO
badge Registry Numbers
MDL Number MFCD23144294
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antidepressant and anxiolytic drugs. Its structure supports the formation of active metabolites that modulate neurotransmitter activity in the central nervous system. Commonly employed in the production of selective serotonin reuptake inhibitors (SSRIs) due to its chiral amine functionality and substituted aromatic ring, which enhance binding affinity to serotonin transporters. Also utilized in research settings for structure-activity relationship (SAR) studies aimed at optimizing drug efficacy and reducing side effects.

Available Sizes & Pricing

Size Availability Unit Price Quantity
50mg
10-20 days ฿5,700.00
100mg
10-20 days ฿9,500.00
2-Amino-2-(4-chloro-3-fluorophenyl)ethan-1-ol hydrochloride
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antidepressant and anxiolytic drugs. Its structure supports the formation of active metabolites that modulate neurotransmitter activity in the central nervous system. Commonly employed in the production of selective serotonin reuptake inhibitors (SSRIs) due to its chiral amine functionality and substituted aromatic ring, which enhance binding affinity to serotonin transporters. Also utilized in research set

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antidepressant and anxiolytic drugs. Its structure supports the formation of active metabolites that modulate neurotransmitter activity in the central nervous system. Commonly employed in the production of selective serotonin reuptake inhibitors (SSRIs) due to its chiral amine functionality and substituted aromatic ring, which enhance binding affinity to serotonin transporters. Also utilized in research settings for structure-activity relationship (SAR) studies aimed at optimizing drug efficacy and reducing side effects.

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