(R)-1-(3,4-Difluorophenyl)ethanamine

≥95%

  • Product Code: 113445
  CAS:    321318-15-4
Molecular Weight: 157.16 g./mol Molecular Formula: C₈H₉F₂N
EC Number: MDL Number: MFCD06761760
Melting Point: Boiling Point: 186.1°C at 760 mmHg
Density: 1.163g/cm3 Storage Condition: 2-8°C, protected from light, stored in an inert gas
Product Description: (R)-1-(3,4-Difluorophenyl)ethanamine is primarily utilized in the pharmaceutical industry as a chiral building block for the synthesis of active pharmaceutical ingredients (APIs). Its enantiomeric purity makes it valuable in the development of drugs that require specific stereochemistry for efficacy, particularly in central nervous system (CNS) therapeutics. It is often employed in the production of selective serotonin reuptake inhibitors (SSRIs) and other psychoactive compounds, where the (R)-configuration is critical for binding to biological targets. Additionally, it serves as an intermediate in the synthesis of agrochemicals, contributing to the creation of pesticides and herbicides with enhanced activity and selectivity. Its role in asymmetric synthesis also extends to the preparation of fine chemicals and specialty materials.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days Ft36,071.71
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1.000 10-20 days Ft85,621.84
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-
5.000 10-20 days Ft257,350.34
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(R)-1-(3,4-Difluorophenyl)ethanamine
(R)-1-(3,4-Difluorophenyl)ethanamine is primarily utilized in the pharmaceutical industry as a chiral building block for the synthesis of active pharmaceutical ingredients (APIs). Its enantiomeric purity makes it valuable in the development of drugs that require specific stereochemistry for efficacy, particularly in central nervous system (CNS) therapeutics. It is often employed in the production of selective serotonin reuptake inhibitors (SSRIs) and other psychoactive compounds, where the (R)-configuration is critical for binding to biological targets. Additionally, it serves as an intermediate in the synthesis of agrochemicals, contributing to the creation of pesticides and herbicides with enhanced activity and selectivity. Its role in asymmetric synthesis also extends to the preparation of fine chemicals and specialty materials.
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