Mehrabi, Hossein team published research in ARKIVOC (Gainesville, FL, United States) in 2021 | 70-23-5

Safety of Ethyl 3-bromo-2-oxopropanoate, Ethyl bromopyruvate molecular formula is C5H7BrO3 and its molecular weight is 195.01 g/mol. The purity is usually 95%.

Ethyl bromopyruvate is used in a synthesis of thioxothiazolidines from carbon disulfide and primary amines.

Ethyl bromopyruvate is a chemical inhibitor that inhibits the enzyme pyruvate dehydrogenase, which is responsible for the conversion of pyruvic acid to acetyl-CoA. This inhibition leads to a decrease in ATP levels and can cause metabolic disorders. Ethyl bromopyruvate is used as an anthelmintic drug and in asymmetric synthesis. It is also used in the synthesis of thiostrepton, an antibiotic that has been shown to have antimicrobial activity against Gram-positive bacteria, including Staphylococcus aureus and Streptococcus pneumoniae., 70-23-5.

Dehydrobromination, Grignard reactions, reductive coupling, Wittig reaction, and several nucleophilic substitution reactions are some of the principal reactions which involve organic bromides. 70-23-5, formula is C5H7BrO3, Name is Ethyl 3-bromo-2-oxopropanoate. Organic compounds having carbon bonded to bromine are called organic bromides. Safety of Ethyl 3-bromo-2-oxopropanoate.

Mehrabi, Hossein;Alizadeh-Bami, Farzaneh;Meydani, Azam;Besharat, Soheila research published 《 An eco-friendly approach for the synthesis of 1,2,5-trisubstituted and 4-amino-1,2,5-tetrasubstituted imidazoles via a multi-component condensation》, the research content is summarized as follows. The synthesis of 1,2,5-trisubstituted imidazoles I (Ar = Ph, 2-chlorophenyl; Ar1 = Ph, 4-tolyl, 4-bromophenyl, etc.) and 4-amino-1,2,5-tetrasubstituted imidazoles II (Ar2 = 4-chlorophenyl, 4-bromophenyl; Ar3 = 4-tolyl, 4-methoxyphenyl, 3-nitrophenyl) was demonstrated via a two-step cyclo-condensation reaction of aryl amines Ar1NH2, carbonitriles ArCN, and Et bromopyruvate or aryl amines Ar3NH2 and arylglyoxals Ar2C(O)CHO in ethanol heated under reflux in the presence of iron (III) chloride (FeCl3), and disodium phosphate (Na2HPO4) as catalysts, resp. All the products I and II were obtained in good to excellent yields and their structures were established from their spectroscopic data.

Safety of Ethyl 3-bromo-2-oxopropanoate, Ethyl bromopyruvate molecular formula is C5H7BrO3 and its molecular weight is 195.01 g/mol. The purity is usually 95%.

Ethyl bromopyruvate is used in a synthesis of thioxothiazolidines from carbon disulfide and primary amines.

Ethyl bromopyruvate is a chemical inhibitor that inhibits the enzyme pyruvate dehydrogenase, which is responsible for the conversion of pyruvic acid to acetyl-CoA. This inhibition leads to a decrease in ATP levels and can cause metabolic disorders. Ethyl bromopyruvate is used as an anthelmintic drug and in asymmetric synthesis. It is also used in the synthesis of thiostrepton, an antibiotic that has been shown to have antimicrobial activity against Gram-positive bacteria, including Staphylococcus aureus and Streptococcus pneumoniae., 70-23-5.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary