(R)-1-[4-(Trifluoromethyl)phenyl]ethylamine

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Reagent Code: #37376
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CAS Number 578027-35-7

science Other reagents with same CAS 578027-35-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 189.1776 g/mol
Formula C₉H₁₀F₃N
badge Registry Numbers
MDL Number MFCD06761837
thermostat Physical Properties
Boiling Point 168.6 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.37g/cm3
Storage room temperature

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) with specific enantiomeric properties. It plays a key role in creating compounds for treating central nervous system disorders, such as antidepressants and antipsychotics. Its trifluoromethyl group enhances the metabolic stability and bioavailability of the final drug molecules. Additionally, it is employed in asymmetric synthesis to produce optically pure intermediates for agrochemicals and fine chemicals.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,284.00

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(R)-1-[4-(Trifluoromethyl)phenyl]ethylamine
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) with specific enantiomeric properties. It plays a key role in creating compounds for treating central nervous system disorders, such as antidepressants and antipsychotics. Its trifluoromethyl group enhances the metabolic stability and bioavailability of the final drug molecules. Additionally, it is employed in asymmetric synthesis to produce optically pure inter

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) with specific enantiomeric properties. It plays a key role in creating compounds for treating central nervous system disorders, such as antidepressants and antipsychotics. Its trifluoromethyl group enhances the metabolic stability and bioavailability of the final drug molecules. Additionally, it is employed in asymmetric synthesis to produce optically pure intermediates for agrochemicals and fine chemicals.

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