2'-Chloroacetoacetanilide

≥98%

Reagent Code: #161072
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CAS Number 93-70-9

science Other reagents with same CAS 93-70-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 211.64 g/mol
Formula C₁₀H₁₀ClNO₂
badge Registry Numbers
MDL Number MFCD00018224
thermostat Physical Properties
Melting Point 107°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used primarily as an intermediate in the synthesis of azo dyes and pigments, especially for producing yellow and orange shades in textile, ink, and paint applications. It plays a key role in the preparation of certain herbicides and pharmaceuticals due to its reactive functional groups. Its acetoacetyl moiety allows for condensation reactions with aromatic amines, making it valuable in organic synthesis for creating nitrogen-containing heterocyclic compounds. Also utilized in the development of agrochemicals, where it contributes to the formation of active ingredients in selective weed control agents.

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿1,100.00
inventory 100g
10-20 days ฿2,570.00
inventory 250g
10-20 days ฿4,570.00
inventory 1kg
10-20 days ฿11,980.00
inventory 5kg
10-20 days ฿56,780.00

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2'-Chloroacetoacetanilide
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Used primarily as an intermediate in the synthesis of azo dyes and pigments, especially for producing yellow and orange shades in textile, ink, and paint applications. It plays a key role in the preparation of certain herbicides and pharmaceuticals due to its reactive functional groups. Its acetoacetyl moiety allows for condensation reactions with aromatic amines, making it valuable in organic synthesis for creating nitrogen-containing heterocyclic compounds. Also utilized in the development of agrochemi

Used primarily as an intermediate in the synthesis of azo dyes and pigments, especially for producing yellow and orange shades in textile, ink, and paint applications. It plays a key role in the preparation of certain herbicides and pharmaceuticals due to its reactive functional groups. Its acetoacetyl moiety allows for condensation reactions with aromatic amines, making it valuable in organic synthesis for creating nitrogen-containing heterocyclic compounds. Also utilized in the development of agrochemicals, where it contributes to the formation of active ingredients in selective weed control agents.

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