(1R,2S)-1-Amino-1-(4-fluorophenyl)propan-2-ol hydrochloride

95%(HPLC)

Reagent Code: #229331
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CAS Number 2828440-04-4

science Other reagents with same CAS 2828440-04-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 205.66 g/mol
Formula C₉H₁₃ClFNO
inventory_2 Storage & Handling
Storage Room temperature, seal, inert gas

description Product Description

Used as a key chiral intermediate in the synthesis of selective serotonin reuptake inhibitors (SSRIs), particularly in the production of antidepressant medications. Its stereochemistry allows for high enantioselectivity in drug synthesis, improving the efficacy and reducing side effects of the final pharmaceutical product. Commonly employed in asymmetric synthesis routes due to its stable amine-alcohol functionality, which readily participates in reductive amination and nucleophilic addition reactions. Also utilized in the preparation of biologically active molecules where fluorinated aromatic moieties enhance metabolic stability and membrane permeability.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿21,450.00
250mg
10-20 days ฿36,440.00
1g
10-20 days ฿98,340.00
(1R,2S)-1-Amino-1-(4-fluorophenyl)propan-2-ol hydrochloride
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Used as a key chiral intermediate in the synthesis of selective serotonin reuptake inhibitors (SSRIs), particularly in the production of antidepressant medications. Its stereochemistry allows for high enantioselectivity in drug synthesis, improving the efficacy and reducing side effects of the final pharmaceutical product. Commonly employed in asymmetric synthesis routes due to its stable amine-alcohol functionality, which readily participates in reductive amination and nucleophilic addition reactions. Also
Used as a key chiral intermediate in the synthesis of selective serotonin reuptake inhibitors (SSRIs), particularly in the production of antidepressant medications. Its stereochemistry allows for high enantioselectivity in drug synthesis, improving the efficacy and reducing side effects of the final pharmaceutical product. Commonly employed in asymmetric synthesis routes due to its stable amine-alcohol functionality, which readily participates in reductive amination and nucleophilic addition reactions. Also utilized in the preparation of biologically active molecules where fluorinated aromatic moieties enhance metabolic stability and membrane permeability.
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