4-ethyl-2-nitrophenol

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Reagent Code: #184046
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CAS Number 56520-98-0

science Other reagents with same CAS 56520-98-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 167.16 g/mol
Formula C₈H₉NO₃
thermostat Physical Properties
Boiling Point 267ºC at 760mmHg
inventory_2 Storage & Handling
Density 1.261g/cm3
Storage Room temperature

description Product Description

Used primarily as an intermediate in the synthesis of agrochemicals and dyes. It serves in the production of certain herbicides and insecticides due to its nitrophenolic structure, which can be further modified to enhance biological activity. Also utilized in research settings for developing novel organic compounds, especially those requiring selective substitution on aromatic rings. Its reactivity allows for transformations such as reductions, alkylations, and coupling reactions in multi-step synthetic pathways.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿2,040.00
inventory 1g
10-20 days ฿2,700.00
inventory 5g
10-20 days ฿9,430.00
inventory 25g
10-20 days ฿33,720.00

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4-ethyl-2-nitrophenol
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Used primarily as an intermediate in the synthesis of agrochemicals and dyes. It serves in the production of certain herbicides and insecticides due to its nitrophenolic structure, which can be further modified to enhance biological activity. Also utilized in research settings for developing novel organic compounds, especially those requiring selective substitution on aromatic rings. Its reactivity allows for transformations such as reductions, alkylations, and coupling reactions in multi-step synthetic

Used primarily as an intermediate in the synthesis of agrochemicals and dyes. It serves in the production of certain herbicides and insecticides due to its nitrophenolic structure, which can be further modified to enhance biological activity. Also utilized in research settings for developing novel organic compounds, especially those requiring selective substitution on aromatic rings. Its reactivity allows for transformations such as reductions, alkylations, and coupling reactions in multi-step synthetic pathways.

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