Ethyl cyanoacetate

CAS : 105-56-6

Ref. 3D-FE60340

Informations sur le produit

• Nom: Ethyl cyanoacetate
• Synonymes: Cyanoacetic acid ethyl ester, (Ethoxycarbonyl)acetonitrile, 2-Cyanoacetic acid ethyl ester, 3-Ethoxy-3-oxopropanenitrile, Acetate, Cyano-, Ethyl, Acetic Acid, Cyano-, Ethylester, Acetic acid, 2-cyano-, ethyl ester, Acetic acid, cyano-, ethyl ester, Cianoacetato De Etilo, Cyanessigsaeure-Aethylester, Cyanoacetate d'ethyle, Cyanoacetic ester, Ethyl 2-cyanoacetate, Ethyl cyanacetate, Ethyl cyanoethanoate, Ethyl α-cyanoacetate, Ethylcyanacetat, Ethyle Cyanacetate, Malonic Ethyl Ester Nitrile, Malonic acid ethyl ester nitrile, Nsc 8844

Description

Ethyl cyanoacetate is a reactive molecule that can be used to measure the redox potential of a solution. The chemical reaction between ethyl cyanoacetate and sodium salts produces an insoluble product, which is coumarin derivatives. Ethyl cyanoacetate has been shown to have anti-inflammatory properties in animal models of inflammatory bowel disease, as well as inhibiting the activity of acetylcholinesterase in rats, which may be due to its structural similarity to acetylcholine. The mechanism for this inhibition has been elucidated by structural biology and chemical reactivity studies. The synthesis of ethyl cyanoacetate involves the conversion of diethyl ketomalonate into ethyl cyanoacetate using anhydrous sodium.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 113.11 g/mol
• Formule: C₅H₇NO₂
• Degré de pureté: Min. 95%
• Couleur/Forme: Clear Liquid
• InChI: InChI=1S/C5H10O2/c1-3-5(6)7-4-2/h3-4H2,1-2H3
• Code InChI: InChIKey=FKRCODPIKNYEAC-UHFFFAOYSA-N
• SMILES: CCOC(=O)CC#N