5-Chloro-2-ethoxyaniline

95%

Reagent Code: #164067
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CAS Number 15793-48-3

science Other reagents with same CAS 15793-48-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 171.62 g/mol
Formula C₈H₁₀ClNO
badge Registry Numbers
MDL Number MFCD07791193
thermostat Physical Properties
Melting Point 21-22 °C
inventory_2 Storage & Handling
Storage Room temperature, dry, light-proof

description Product Description

Used primarily as an intermediate in the synthesis of azo dyes and pigments, particularly for producing yellow and orange shades in textile, leather, and printing ink applications. It also serves in the manufacture of certain agrochemicals, including herbicides and pesticides, due to its reactivity in forming carbon-nitrogen bonds. Its chloro and amino functional groups allow for easy modification in organic reactions, making it valuable in pharmaceutical research for building more complex molecules. Additionally, it is employed in the production of specialty polymers where aromatic amines contribute to thermal stability and mechanical strength.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿620.00
inventory 250mg
10-20 days ฿1,330.00
inventory 1g
10-20 days ฿3,880.00

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5-Chloro-2-ethoxyaniline
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Used primarily as an intermediate in the synthesis of azo dyes and pigments, particularly for producing yellow and orange shades in textile, leather, and printing ink applications. It also serves in the manufacture of certain agrochemicals, including herbicides and pesticides, due to its reactivity in forming carbon-nitrogen bonds. Its chloro and amino functional groups allow for easy modification in organic reactions, making it valuable in pharmaceutical research for building more complex molecules. Add

Used primarily as an intermediate in the synthesis of azo dyes and pigments, particularly for producing yellow and orange shades in textile, leather, and printing ink applications. It also serves in the manufacture of certain agrochemicals, including herbicides and pesticides, due to its reactivity in forming carbon-nitrogen bonds. Its chloro and amino functional groups allow for easy modification in organic reactions, making it valuable in pharmaceutical research for building more complex molecules. Additionally, it is employed in the production of specialty polymers where aromatic amines contribute to thermal stability and mechanical strength.

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