N-(3-chlorophenyl)-maleimide

95%

Reagent Code: #219696
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CAS Number 1204-35-9

science Other reagents with same CAS 1204-35-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 207.618 g/mol
Formula C₁₀H₆ClNO₂
badge Registry Numbers
MDL Number MFCD00022570
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of functional polymers and specialty resins, particularly in the development of high-performance thermosetting materials. Its reactive maleimide group enables participation in Michael addition reactions and radical polymerizations, making it valuable in creating crosslinked networks for coatings, adhesives, and composites with enhanced thermal and chemical resistance. Also employed in the modification of proteins and biomolecules for research applications due to its selective reactivity with thiol and amine groups. Additionally, it serves as a building block in the preparation of pharmaceuticals and agrochemicals where aromatic and imide functionalities are required.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,520.00
inventory 1g
10-20 days ฿7,250.00
inventory 5g
10-20 days ฿24,260.00
inventory 25g
10-20 days ฿88,020.00

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N-(3-chlorophenyl)-maleimide
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Used as a key intermediate in the synthesis of functional polymers and specialty resins, particularly in the development of high-performance thermosetting materials. Its reactive maleimide group enables participation in Michael addition reactions and radical polymerizations, making it valuable in creating crosslinked networks for coatings, adhesives, and composites with enhanced thermal and chemical resistance. Also employed in the modification of proteins and biomolecules for research applications due t

Used as a key intermediate in the synthesis of functional polymers and specialty resins, particularly in the development of high-performance thermosetting materials. Its reactive maleimide group enables participation in Michael addition reactions and radical polymerizations, making it valuable in creating crosslinked networks for coatings, adhesives, and composites with enhanced thermal and chemical resistance. Also employed in the modification of proteins and biomolecules for research applications due to its selective reactivity with thiol and amine groups. Additionally, it serves as a building block in the preparation of pharmaceuticals and agrochemicals where aromatic and imide functionalities are required.

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