CAS 197376-41-3

Ethyl 2-(3-bromopyridin-2-yl)acetate

Description:

Ethyl 2-(3-bromopyridin-2-yl)acetate is an organic compound characterized by its ester functional group, which is derived from acetic acid and ethanol. The presence of a bromine atom on the pyridine ring introduces notable reactivity and influences the compound's physical and chemical properties. This compound typically appears as a colorless to pale yellow liquid with a distinctive odor. It is soluble in organic solvents such as ethanol and dichloromethane but has limited solubility in water due to its hydrophobic ethyl group. The bromopyridine moiety can participate in various chemical reactions, making this compound useful in synthetic organic chemistry, particularly in the development of pharmaceuticals and agrochemicals. Its molecular structure allows for potential applications in medicinal chemistry, where the bromine substituent can enhance biological activity or facilitate further chemical modifications. As with many organic compounds, safety precautions should be observed when handling this substance, as it may pose health risks if ingested or inhaled.

2-​Pyridineacetic acid, 3-​bromo-​, ethyl ester

CAS: 197376-41-3

Formula: C₉H₁₀BrNO₂

Purity: 98%

Color and Shape: Liquid

Molecular weight: 244.0852

Ref: IN-DA002ASB

Ethyl 2-(3-bromopyridin-2-yl)acetate

CAS: 197376-41-3

Ethyl 2-(3-bromopyridin-2-yl)acetate

Purity: 99%

Molecular weight: 244.09g/mol

Ref: 54-OR76114

Ethyl 2-(3-bromopyridin-2-yl)acetate

CAS: 197376-41-3

Formula: C₉H₁₀BrNO₂

Purity: 98%

Color and Shape: Liquid

Molecular weight: 244.088

Ref: 10-F232079

Ethyl 2-(3-bromopyridin-2-yl)acetate

CAS: 197376-41-3

Ethyl 2-(3-bromopyridin-2-yl)acetate is a synthetic compound that has been used in the treatment of cancer. It has been shown to be effective against colon cancer and cancer cell lines. Ethyl 2-(3-bromopyridin-2-yl)acetate binds to DNA and inhibits the activity of topoisomerase II, which is an enzyme that maintains the integrity of DNA. This inhibition leads to disruption of DNA synthesis and replication, leading to cell death. The antitumour activity of this compound is due to its ability to create reactive oxygen species (ROS), which lead to oxidative stress in cells.

Formula: C₉H₁₀BrNO₂

Purity: Min. 95%

Molecular weight: 244.09 g/mol

Ref: 3D-XHA37641