N-Ethylmaleimide (CAS 128-53-0): Applications in Organic Synthesis
Organic synthesis is the bedrock of many modern industries, from pharmaceuticals and agrochemicals to advanced materials. Within this complex field, specific chemical intermediates are indispensable for building intricate molecular structures. N-Ethylmaleimide (CAS 128-53-0) is one such versatile compound, prized for its reactivity and utility in a variety of synthetic pathways. As a leading specialty chemical manufacturer and supplier in China, we are dedicated to providing high-purity N-Ethylmaleimide to researchers and industrial chemists worldwide. This article highlights the key applications of N-Ethylmaleimide in organic synthesis and guides procurement specialists on how to source this essential material.
The maleimide functional group within N-Ethylmaleimide is a powerful electrophile, readily undergoing addition reactions with nucleophiles. This characteristic makes it a valuable component in numerous synthetic transformations:
- Diels-Alder Reactions: The double bond in the maleimide ring can participate in [4+2] cycloaddition reactions, commonly known as Diels-Alder reactions. These reactions are fundamental for constructing cyclic systems, which are prevalent in natural products and pharmaceuticals. N-Ethylmaleimide acts as a reactive dienophile, enabling the synthesis of complex polycyclic frameworks.
- Michael Additions: As previously discussed in the context of protein crosslinking, N-Ethylmaleimide readily undergoes Michael addition with various nucleophiles, including thiols, amines, and carbanions. This reaction is a versatile tool for carbon-carbon and carbon-heteroatom bond formation, allowing for the introduction of functional groups and the extension of carbon chains.
- Synthesis of Heterocycles: The structure of N-Ethylmaleimide lends itself to the synthesis of various nitrogen-containing heterocycles, which are important structural motifs in many biologically active compounds. Through carefully designed reaction sequences, the maleimide core can be transformed into a range of complex heterocyclic systems.
- Polymerization Monomer: N-Ethylmaleimide can also serve as a monomer or co-monomer in the synthesis of specialty polymers. Its incorporation into polymer chains can impart unique properties such as thermal stability or specific chemical reactivity.
For R&D scientists and procurement managers looking to purchase N-Ethylmaleimide, consistency and purity are paramount. Our commitment as a manufacturer in China ensures that we supply N-Ethylmaleimide with a guaranteed purity of 98% HPLC. This high level of purity is critical for achieving reproducible results in organic synthesis and minimizing the formation of unwanted byproducts. We encourage you to request a quote to explore our competitive pricing and discuss your specific quantity requirements.
Sourcing directly from a reputable Chinese manufacturer offers distinct advantages, including cost-effectiveness and a reliable supply chain. We understand that timely delivery of raw materials is crucial for maintaining project timelines and operational efficiency. Our robust logistics network ensures that N-Ethylmaleimide reaches your facility efficiently.
In conclusion, N-Ethylmaleimide (CAS 128-53-0) is a highly valuable intermediate in organic synthesis, enabling key reactions like Diels-Alder cycloadditions and Michael additions for the construction of complex molecules. As a trusted supplier, we provide high-purity material backed by strong manufacturing capabilities. Make N-Ethylmaleimide a staple in your synthetic chemistry toolkit by sourcing from a dependable Chinese manufacturer and supplier.
Perspectives & Insights
Silicon Analyst 88
“The maleimide functional group within N-Ethylmaleimide is a powerful electrophile, readily undergoing addition reactions with nucleophiles.”
Quantum Seeker Pro
“This characteristic makes it a valuable component in numerous synthetic transformations: Diels-Alder Reactions: The double bond in the maleimide ring can participate in [4+2] cycloaddition reactions, commonly known as Diels-Alder reactions.”
Bio Reader 7
“These reactions are fundamental for constructing cyclic systems, which are prevalent in natural products and pharmaceuticals.”