CAS 134448-46-7

5-(2,4-Dichlorophenyl)-2-furoic acid

Description:

5-(2,4-Dichlorophenyl)-2-furoic acid is an organic compound characterized by its furoic acid structure, which features a furan ring fused with a carboxylic acid group. The presence of the 2,4-dichlorophenyl substituent introduces significant polarity and potential for hydrogen bonding due to the electronegative chlorine atoms. This compound typically exhibits solid-state properties at room temperature and is likely to be sparingly soluble in water, while being more soluble in organic solvents. Its molecular structure suggests potential applications in pharmaceuticals or agrochemicals, particularly as an intermediate in the synthesis of biologically active compounds. The compound may also exhibit specific reactivity patterns due to the functional groups present, making it of interest in various chemical reactions. Safety data should be consulted for handling and storage, as the presence of chlorine atoms may indicate potential toxicity or environmental hazards. Overall, 5-(2,4-Dichlorophenyl)-2-furoic acid is a compound of interest in organic chemistry with diverse applications.

Formula: C₁₁H₆Cl₂O₃

InChI: InChI=1/C11H6Cl2O3/c12-6-1-2-7(8(13)5-6)9-3-4-10(16-9)11(14)15/h1-5H,(H,14,15)

SMILES: c1cc(c(cc1Cl)Cl)c1ccc(C(=O)O)o1

Synonyms:

• 5-(2,4-Dichlorophenyl)Furan-2-Carboxylic Acid

5-(2,4-Dichlorophenyl)-2-furoic acid

CAS: 134448-46-7

Formula: C₁₁H₆Cl₂O₃

Color and Shape: Solid

Molecular weight: 257.0695

Ref: IN-DA003M39

5-(2,4-Dichlorophenyl)-2-furoic acid

CAS: 134448-46-7

5-(2,4-Dichlorophenyl)-2-furoic acid is an antibacterial agent that has been shown to have a cytotoxic effect on tumor cells. The biological activity of this compound has been shown in vitro and in vivo. 5-(2,4-Dichlorophenyl)-2-furoic acid has been found to inhibit the growth of tumor cells by interfering with their metabolism and inhibiting the synthesis of DNA, RNA and proteins. 5-(2,4-Dichlorophenyl)-2-furoic acid also inhibits the growth of microorganisms such as Enterococcus faecalis. This antibiotic has been shown to destroy bacterial cell walls by oxidation of chitin at the interface between the cell wall and cytoplasmic membrane. The mechanism for this action is not yet clear, but it may involve photoelectrical effects or generation of reactive oxygen species.

Formula: C₁₁H₆Cl₂O₃

Purity: Min. 95%

Molecular weight: 257.07 g/mol

Ref: 3D-JFA44846