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AD27510

134272-64-3 | 2-Maleimidoethylamine HCl

Packsize Purity Availability Price Discounted Price    Quantity
100mg 96% in stock $6.00 $4.00 -   +
250mg 96% in stock $8.00 $5.00 -   +
1g 96% in stock $20.00 $14.00 -   +
5g 96% in stock $66.00 $46.00 -   +
25g 96% in stock $265.00 $186.00 -   +
100g 96% in stock $875.00 $613.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AD27510
Chemical Name: 2-Maleimidoethylamine HCl
CAS Number: 134272-64-3
Molecular Formula: C6H9ClN2O2
Molecular Weight: 176.6009
MDL Number: MFCD09800491
SMILES: NCCN1C(=O)C=CC1=O.Cl

 

Computed Properties
Complexity: 180  
Covalently-Bonded Unit Count: 2  
Heavy Atom Count: 11  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 2  

 

 

Upstream Synthesis Route
  • 1-(2-Aminoethyl)-1H-pyrrole-2,5-dione hydrochloride, also known as $name$, plays a crucial role in chemical synthesis as a versatile starting material. This compound is frequently utilized in the production of various pharmaceuticals, agrochemicals, and specialty chemicals due to its unique chemical structure and reactivity.In organic synthesis, $name$ serves as a key intermediate in the construction of complex molecules. Its amino and pyrrole functional groups offer opportunities for selective derivatization, enabling the formation of diverse chemical bonds and stereochemistries. The presence of the hydrochloride moiety enhances the compound's solubility and facilitates its manipulation in different reaction conditions.Moreover, 1-(2-Aminoethyl)-1H-pyrrole-2,5-dione hydrochloride is employed in the synthesis of novel heterocyclic compounds and peptidomimetics. Its ability to participate in diverse coupling reactions and cyclization processes makes it a valuable building block for designing bioactive molecules with potential therapeutic applications.Overall, the strategic incorporation of $name$ in chemical synthesis enables the efficient production of structurally diverse compounds with tailored properties, showcasing its significance in the advancement of modern chemistry and drug discovery processes.
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