Methyl 4-bromothiophene-2-carboxylate is an organic compound characterized by its thiophene ring, which is a five-membered aromatic heterocycle containing sulfur. The presence of a bromine atom at the 4-position and a carboxylate group at the 2-position contributes to its reactivity and potential applications in organic synthesis. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its purity and form. It is soluble in organic solvents such as ethanol and dichloromethane, but has limited solubility in water due to its hydrophobic thiophene structure. Methyl 4-bromothiophene-2-carboxylate can participate in various chemical reactions, including nucleophilic substitutions and coupling reactions, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Safety precautions should be taken when handling this compound, as it may pose health risks if inhaled or ingested, and appropriate personal protective equipment should be used.

Methyl 4-bromothiophene-2-carboxylate

62224-16-2: 4-Bromo-2-(carbomethoxy)thiophene, 4-Bromo-2-thiophenecarboxylic acid methyl ester

Methyl 4-bromothiophene-2-carboxylate is a dehydrohalogenated mesomeric quinolinium compound with a fluorescence emission maximum at 421 nm. It has been found to be an intermediate in the synthesis of betaines. In addition, it has been used to synthesize carboxylates and chlorides. Methyl 4-bromothiophene-2-carboxylate is also known to be a metabolite of malignant cells that can be used as a biomarker for pancreatic cancer and chronic pancreatitis, as well as being an alkylating agent.

CAS 62224-16-2: Methyl 4-bromothiophene-2-carboxylate

Methyl 4-bromothiophene-2-carboxylate

Ref: 54-OR17259

Methyl 4-bromothiophene-2-carboxylate

Ref: 3D-FM140559

Methyl 4-bromothiophene-2-carboxylate

Ref: IN-DA00EFUC

Methyl 4-bromothiophene-2-carboxylate

Ref: 10-F228151