3-Acetamidophenyl acetate

98%

Reagent Code: #137755
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CAS Number 6317-89-1

science Other reagents with same CAS 6317-89-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 193.20 g/mol
Formula C₁₀H₁₁NO₃
badge Registry Numbers
MDL Number MFCD00465580
thermostat Physical Properties
Boiling Point 377.2 °C at 764 mmHg
inventory_2 Storage & Handling
Density 1.206 g/cm3(Predicted)
Storage Room temperature, sealed, dry

description Product Description

Used primarily as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and fine chemicals. It serves as a protected form of 3-aminophenol, allowing selective reactions at other functional sites during multi-step syntheses. Commonly employed in the development of analgesics and anti-inflammatory agents due to its structural similarity to acetaminophen. Also utilized in the preparation of dyes and UV absorbers for polymers, offering stability against photodegradation. Its acetyl-protected amine and phenolic groups make it valuable in peptide synthesis and in the creation of specialty esters for cosmetic formulations.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿920.00
inventory 250mg
10-20 days ฿1,290.00
inventory 1g
10-20 days ฿3,870.00

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3-Acetamidophenyl acetate
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Used primarily as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and fine chemicals. It serves as a protected form of 3-aminophenol, allowing selective reactions at other functional sites during multi-step syntheses. Commonly employed in the development of analgesics and anti-inflammatory agents due to its structural similarity to acetaminophen. Also utilized in the preparation of dyes and UV absorbers for polymers, offering stability against photodegradation. Its

Used primarily as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and fine chemicals. It serves as a protected form of 3-aminophenol, allowing selective reactions at other functional sites during multi-step syntheses. Commonly employed in the development of analgesics and anti-inflammatory agents due to its structural similarity to acetaminophen. Also utilized in the preparation of dyes and UV absorbers for polymers, offering stability against photodegradation. Its acetyl-protected amine and phenolic groups make it valuable in peptide synthesis and in the creation of specialty esters for cosmetic formulations.

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