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CAS 52679-49-9

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3-(2-bromo-4,5-dimethoxyphenyl)propanoic acid

Description:
3-(2-Bromo-4,5-dimethoxyphenyl)propanoic acid, with the CAS number 52679-49-9, is an organic compound characterized by its propanoic acid backbone substituted with a brominated aromatic ring. The presence of the bromine atom and two methoxy groups on the aromatic ring significantly influences its chemical properties, including its reactivity and solubility. This compound typically exhibits moderate solubility in organic solvents and may have limited solubility in water due to the hydrophobic nature of the aromatic system. The methoxy groups can participate in hydrogen bonding, potentially affecting its interactions in biological systems. As a carboxylic acid, it can undergo typical acid-base reactions, forming salts and esters. The bromine substituent may also impart unique reactivity, making it a useful intermediate in organic synthesis. Overall, this compound's structure suggests potential applications in medicinal chemistry and material science, particularly in the development of pharmaceuticals or as a building block in organic synthesis.
Formula:C11H13BrO4
InChI:InChI=1/C11H13BrO4/c1-15-9-5-7(3-4-11(13)14)8(12)6-10(9)16-2/h5-6H,3-4H2,1-2H3,(H,13,14)
InChI key:SJTJBIRPIITRRT-UHFFFAOYSA-N
SMILES:COc1cc(CCC(=O)O)c(cc1OC)Br
Synonyms:
  • Benzenepropanoic Acid, 2-Bromo-4,5-Dimethoxy-
  • 3-(2-Bromo-4,5-dimethoxyphenyl)propanoic acid
  • Benzenepropanoic acid, 2-bromo-4,5-dimethoxy- (9CI)
  • 2-BROMO-4,5-DIMETHOXYHYDROCINNAMIC ACID
  • 2-Bromo-4,5-dimethoxy-Benzenepropanoic Acid (9CI)
  • 5-diMethoxy-
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