4'-Methoxyacetoacetanilide

99%

Reagent Code: #205380
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CAS Number 5437-98-9

science Other reagents with same CAS 5437-98-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 207.23 g/mol
Formula C₁₁H₁₃NO₃
badge Registry Numbers
EC Number 226-615-6
MDL Number MFCD00008783
thermostat Physical Properties
Melting Point 115-118 °C
inventory_2 Storage & Handling
Storage Room temperature

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, ink, and coating applications. It plays a key role in diazotization and coupling reactions, contributing to color development and stability in dye formulations. Also utilized in the preparation of certain pharmaceuticals and agrochemicals where anilide derivatives are required. Its methoxy and acetoacetamide functional groups enhance reactivity and solubility, making it suitable for fine chemical synthesis.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿240.00
25g
10-20 days ฿630.00
100g
10-20 days ฿730.00
500g
10-20 days ฿1,347.50
2.5kg
10-20 days ฿12,190.00
4'-Methoxyacetoacetanilide
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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, ink, and coating applications. It plays a key role in diazotization and coupling reactions, contributing to color development and stability in dye formulations. Also utilized in the preparation of certain pharmaceuticals and agrochemicals where anilide derivatives are required. Its methoxy and acetoacetamide functional groups enhance reactivity and solubility, makin

Used primarily as an intermediate in the synthesis of azo dyes and pigments, particularly for producing yellow and orange shades in textile, ink, and coating applications. It plays a key role in diazotization and coupling reactions, contributing to color development and stability in dye formulations. Also utilized in the preparation of certain pharmaceuticals and agrochemicals where anilide derivatives are required. Its methoxy and acetoacetamide functional groups enhance reactivity and solubility, making it suitable for fine chemical synthesis.

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