N-(2-chloroethyl)phthalimide

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Reagent Code: #218404
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CAS Number 6270-06-0

science Other reagents with same CAS 6270-06-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 209.629 g/mol
Formula C₁₀H₈ClNO₂
badge Registry Numbers
MDL Number MFCD00129356
thermostat Physical Properties
Melting Point 82-84 °C
Boiling Point 328.2 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the preparation of nitrogen-containing compounds. It serves as a protected form of 2-chloroethylamine, allowing selective alkylation in pharmaceutical synthesis. Commonly employed in the production of heterocyclic compounds and bioactive molecules, including certain antitumor agents and neurological drugs. Its stability and reactivity make it valuable in ring-opening reactions and in the construction of complex amine architectures.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,590.00
inventory 10g
10-20 days ฿2,870.00
inventory 25g
10-20 days ฿6,400.00

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N-(2-chloroethyl)phthalimide
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Used primarily as an intermediate in organic synthesis, especially in the preparation of nitrogen-containing compounds. It serves as a protected form of 2-chloroethylamine, allowing selective alkylation in pharmaceutical synthesis. Commonly employed in the production of heterocyclic compounds and bioactive molecules, including certain antitumor agents and neurological drugs. Its stability and reactivity make it valuable in ring-opening reactions and in the construction of complex amine architectures.

Used primarily as an intermediate in organic synthesis, especially in the preparation of nitrogen-containing compounds. It serves as a protected form of 2-chloroethylamine, allowing selective alkylation in pharmaceutical synthesis. Commonly employed in the production of heterocyclic compounds and bioactive molecules, including certain antitumor agents and neurological drugs. Its stability and reactivity make it valuable in ring-opening reactions and in the construction of complex amine architectures.

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