2-Fluoro-5-(trifluoromethyl)aniline

97%

Reagent Code: #59120
label
Alias 3-Amino-4-fluorobenzotrifluoride 4-fluoro-3-aminobenzotrifluoride 2-fluoro-5-trifluoromethylaniline
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CAS Number 535-52-4

science Other reagents with same CAS 535-52-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 179.12 g/mol
Formula C₇H₅F₄N
badge Registry Numbers
MDL Number MFCD00007653
thermostat Physical Properties
Boiling Point 155 °C(lit.)
inventory_2 Storage & Handling
Density 1.378 g/mL at 25 °C(lit.)
Storage room temperature

description Product Description

This chemical is primarily utilized in the synthesis of pharmaceutical compounds and agrochemicals. It serves as a key intermediate in the production of active ingredients for drugs targeting various diseases, including cancer and infections, due to its unique fluorine-containing structure that enhances biological activity. In agriculture, it is employed in the development of herbicides and pesticides, where its trifluoromethyl group contributes to improved efficacy and stability. Additionally, it finds applications in organic synthesis for creating complex molecules used in material science and specialty chemicals.

format_list_bulleted Product Specification

Test Parameter Specification
Purity (GC) 96.5-100%
Purity (Titration by HClO4) 96.5-102.5%
Refractive Index (n20D) 1.46-1.462
Specific Gravity (2020) 1.397-1.4
Appearance Colorless to amber liquid
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿280.00
inventory 5g
10-20 days ฿300.00
inventory 25g
10-20 days ฿700.00
inventory 100g
10-20 days ฿2,650.00

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2-Fluoro-5-(trifluoromethyl)aniline
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This chemical is primarily utilized in the synthesis of pharmaceutical compounds and agrochemicals. It serves as a key intermediate in the production of active ingredients for drugs targeting various diseases, including cancer and infections, due to its unique fluorine-containing structure that enhances biological activity. In agriculture, it is employed in the development of herbicides and pesticides, where its trifluoromethyl group contributes to improved efficacy and stability. Additionally, it finds applications in organic synthesis for creating complex molecules used in material science and specialty chemicals.
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