(R)-1-(4-Chloro-3-fluorophenyl)ethanamine hydrochloride

98%

Reagent Code: #113454
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CAS Number 1253790-80-5

science Other reagents with same CAS 1253790-80-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 210.08 g/mol
Formula C₈H₁₀Cl₂FN
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its chiral structure makes it particularly valuable in the development of enantioselective drugs, where the specific stereochemistry can significantly influence the drug's efficacy and safety profile. It is often employed in the production of medications targeting central nervous system disorders, including antidepressants and antipsychotics, due to its ability to interact with neurotransmitter systems. Additionally, its halogenated aromatic ring contributes to its role in creating compounds with enhanced binding affinity and metabolic stability, making it a crucial building block in drug discovery and development processes.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,268.00
inventory 1g
10-20 days ฿6,768.00
inventory 50mg
10-20 days ฿540.00

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(R)-1-(4-Chloro-3-fluorophenyl)ethanamine hydrochloride
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This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its chiral structure makes it particularly valuable in the development of enantioselective drugs, where the specific stereochemistry can significantly influence the drug's efficacy and safety profile. It is often employed in the production of medications targeting central nervous system disorders, including antidepressants and antipsychotics, due t

This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its chiral structure makes it particularly valuable in the development of enantioselective drugs, where the specific stereochemistry can significantly influence the drug's efficacy and safety profile. It is often employed in the production of medications targeting central nervous system disorders, including antidepressants and antipsychotics, due to its ability to interact with neurotransmitter systems. Additionally, its halogenated aromatic ring contributes to its role in creating compounds with enhanced binding affinity and metabolic stability, making it a crucial building block in drug discovery and development processes.

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