trans-Ethyl 4-bromocrotonate

CAS : 37746-78-4

Ref. 3D-FE36836

Informations sur le produit

• Nom: trans-Ethyl 4-bromocrotonate
• Synonymes: (E)-Ethyl 4-bromocrotonate, (2E)-4-Bromo-2-butenoic acid ethyl ester, (E)-4-Bromo-2-butenoic acid ethyl ester, (E)-4-Bromobut-2-enoic acid ethyl ester, (E)-ethyl 4-bromobut-2-enoate, 2-Butenoic acid, 4-bromo-, ethyl ester, 2-Butenoic acid, 4-bromo-, ethyl ester, (2E)-, 2-Butenoic acid, 4-bromo-, ethyl ester, (E)-, 4-Bromocrotonic acid ethyl ester, Ai3-52372, Ethyl (E)-4-bromo-2-butenoate, Ethyl (E)-4-bromobutenoate, Ethyl (E)-4-bromocrotonate, Ethyl 4-bromo-2-(E)-butenoate, Ethyl bromocrotonate, Ethyl trans-4-bromo-2-butenoate, Ethylbromocrotonatepract, ethyl (2E)-4-bromobut-2-enoate, ethyl (2Z)-4-bromobut-2-enoate, trans-Ethyl γ-bromocrotonate

Description

Trans-ethyl 4-bromocrotonate is an organic compound that belongs to the class of aldehydes. It is used as a building block in the synthesis of indole-3-pyruvic acid and other β-amino acids, which are biologically active compounds. Trans-ethyl 4-bromocrotonate can be prepared by reacting allyl bromide with ethyl acetoacetate in the presence of hydrochloric acid and sodium salts. The reaction proceeds efficiently at room temperature, making it an efficient method for the preparation of this compound. Trans-ethyl 4-bromocrotonate has been shown to inhibit the activity of pancreatic lipase and may also inhibit other enzymes such as cholesterol esterase or lecithinase. This inhibition activity may be due to its ability to act as an acceptor for halides in these reactions.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 193.04 g/mol
• Formule: C₆H₉BrO₂
• Degré de pureté: Min. 95%
• Couleur/Forme: Liquid
• InChI: InChI=1S/C6H9BrO2/c1-2-9-6(8)4-3-5-7/h3-4H,2,5H2,1H3/b4-3+
• Code InChI: InChIKey=FHGRPBSDPBRTLS-ONEGZZNKSA-N
• SMILES: CCOC(=O)/C=C/CBr