2-Acetyl-5-bromothiophene

CAS : 5370-25-2

Ref. 3D-FA36703

Informations sur le produit

• Nom: 2-Acetyl-5-bromothiophene
• Synonymes: 1-(5-Bromo-2-thienyl)ethanone, 1-(5-Bromothien-2-Yl)Ethanone, 1-(5-Bromothiophen-2-Yl)Ethanone, 1-(5-Bromothiophen-2-yl)ethan-1-one, 2-Acetyl-5-bromthiophen, 2-Bromo-5-acetylthiophene, 5-Acetyl-2-bromothiophene, 5-Bromo-2-acetylthiophene, Ethanone, 1- (5-bromo-2-thienyl)-, Ketone, 5-bromo-2-thienyl methyl, NSC 80366

Description

2-Acetyl-5-bromothiophene is an organosulfur compound that is a reactive intermediate in the Suzuki coupling reaction. It has been used as a substrate for biological studies of toxicity and cancer, and to generate unsymmetrical compounds with multi-walled carbon light emission. 2-Acetyl-5-bromothiophene also has the ability to inhibit glutamate dehydrogenase and hydroxide solution, which are enzymes necessary for the production of energy in cells. 2-Acetyl-5-bromothiophene is toxic to animals and humans because it can cause cancer and other health problems such as neurotoxicity, liver dysfunction, and kidney damage. 2-Acetyl-5-bromothiophene has been shown to cause DNA strand breaks in human breast cancer cells.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 205.07 g/mol
• Formule: C₆H₅BrOS
• Degré de pureté: Min. 98.5 Area-%
• Couleur/Forme: Powder
• InChI: InChI=1S/C6H5BrOS/c1-4(8)5-2-3-6(7)9-5/h2-3H,1H3
• Code InChI: InChIKey=IGBZCOWXSCWSHO-UHFFFAOYSA-N
• SMILES: CC(=O)c1ccc(Br)s1