N-(4-Chlorophenyl)phthalimide

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Reagent Code: #217791
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CAS Number 7386-21-2

science Other reagents with same CAS 7386-21-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 257.67 g/mol
Formula C₁₄H₈ClNO₂
thermostat Physical Properties
Melting Point 196.0-200.0°C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a building block for the development of bioactive molecules due to the presence of the phthalimide group, which is known for its stability and ability to participate in various substitution reactions. Commonly employed in the synthesis of herbicides and fungicides, it also finds use in research settings for the construction of nitrogen-containing heterocyclic compounds. Its chloroaryl moiety enhances reactivity in cross-coupling reactions, making it valuable in medicinal chemistry for designing new drug candidates.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿840.00
inventory 5g
10-20 days ฿2,730.00
inventory 25g
10-20 days ฿9,440.00
inventory 100g
10-20 days ฿28,790.00

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N-(4-Chlorophenyl)phthalimide
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a building block for the development of bioactive molecules due to the presence of the phthalimide group, which is known for its stability and ability to participate in various substitution reactions. Commonly employed in the synthesis of herbicides and fungicides, it also finds use in research settings for the construction of nitrogen-containing heterocyclic compounds. Its chl

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a building block for the development of bioactive molecules due to the presence of the phthalimide group, which is known for its stability and ability to participate in various substitution reactions. Commonly employed in the synthesis of herbicides and fungicides, it also finds use in research settings for the construction of nitrogen-containing heterocyclic compounds. Its chloroaryl moiety enhances reactivity in cross-coupling reactions, making it valuable in medicinal chemistry for designing new drug candidates.

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