(E)-Ethyl 3-ethoxyacrylate

CAS : 5941-55-9

Ref. 3D-FE165489

Informations sur le produit

• Nom: (E)-Ethyl 3-ethoxyacrylate
• Synonymes: 2-Propenoic acid, 3-ethoxy-, ethyl ester, (2E)-, 2-Propenoic acid, 3-ethoxy-, ethyl ester, (E)-, 3-Eae, 3-Ethoxyacrylic Acid Ethyl Ester, Beta-Ethoxyacrylic Acid Ethyl Ester, Ethoxyacrylic acid ethyl ester, 97%, Ethyl (2-E)-3-ethoxyprop-2-enoate, Ethyl (2E)-3-ethoxy-2-propenoate, Ethyl (E)-3-ethoxy-2-propenoate, Ethyl (E)-3-ethoxyacrylate, Ethyl 3-Ethoxy-2-Propenoate, Ethyl 3-Ethoxyacrylate Stab., Ethyl 3-Ethoxyprop-2-Enoate, Ethyl trans-3-ethoxyacrylate, Ethyl3-ethoxyacrylate, ethyl (2E)-3-ethoxyacrylate, ethyl (E)-3-ethoxyprop-2-enoate, Á-Ethoxyacrylic Acid Ethyl Ester

Description

(E)-Ethyl 3-ethoxyacrylate is a reactive electrophile, which can be used to synthesize a variety of organic compounds. It is the ethyl ester of acrylic acid and has been shown to react with azides, halides, and other electrophiles. For example, (E)-ethyl 3-ethoxyacrylate reacts with ethidium bromide to yield an iminium cation and an azo compound. The reaction mechanism for this reaction proceeds as follows:

(E)-Ethyl 3-ethoxyacrylate + Ethidium bromide → (E)-Ethyl 3-ethoxyacrylate cation + Azo compound

The product distribution depends on the pH of the solution. At low pH, the product is the iminium cation; at high pH, it is the azo compound.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 144.17 g/mol
• Formule: C₇H₁₂O₃
• Degré de pureté: Min. 95%
• InChI: InChI=1S/C7H12O3/c1-3-9-6-5-7(8)10-4-2/h5-6H,3-4H2,1-2H3/b6-5+
• Code InChI: InChIKey=ITQFPVUDTFABDH-AATRIKPKSA-N
• SMILES: CCO/C=C/C(=O)OCC