4'-Amino-3'-(trifluoromethyl)acetanilide

98%

Reagent Code: #136411
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CAS Number 1579-89-1

science Other reagents with same CAS 1579-89-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 218.18 g/mol
Formula C₉H₉F₃N₂O
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system active agents. It serves as a building block in the development of fluorinated organic compounds, where the trifluoromethyl group enhances metabolic stability and bioavailability. Also employed in the preparation of agrochemicals and specialty polymers due to its electron-withdrawing properties and structural resilience. Its amino and amide functionalities allow for further chemical modifications, making it valuable in medicinal chemistry research and development.

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Test Parameter Specification
Appearance Report Result
Purity (Nonaqueous Titration)(%) 98-102
Melting Point (C) 118-122
NMR confirm to structure
Melting Point (°C) 118-122

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿1,320.00
4'-Amino-3'-(trifluoromethyl)acetanilide
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system active agents. It serves as a building block in the development of fluorinated organic compounds, where the trifluoromethyl group enhances metabolic stability and bioavailability. Also employed in the preparation of agrochemicals and specialty polymers due to its electron-withdrawing properties and structural resilience. Its amino

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system active agents. It serves as a building block in the development of fluorinated organic compounds, where the trifluoromethyl group enhances metabolic stability and bioavailability. Also employed in the preparation of agrochemicals and specialty polymers due to its electron-withdrawing properties and structural resilience. Its amino and amide functionalities allow for further chemical modifications, making it valuable in medicinal chemistry research and development.

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