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CAS 35207-70-6

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trans-3-Chlorocyclobutanecarboxylic acid

Description:
Trans-3-Chlorocyclobutanecarboxylic acid is a cyclic carboxylic acid characterized by a cyclobutane ring with a chlorine substituent at the 3-position and a carboxylic acid functional group. This compound exhibits a unique three-dimensional structure due to the constraints of the cyclobutane ring, which can influence its reactivity and interactions with other molecules. The presence of the chlorine atom introduces both electronegative character and steric effects, potentially affecting the compound's acidity and reactivity in chemical reactions. As a carboxylic acid, it can participate in typical acid-base reactions, forming salts and esters. The trans configuration indicates that the chlorine and carboxylic acid groups are positioned on opposite sides of the ring, which can impact the compound's physical properties, such as boiling and melting points, as well as its solubility in various solvents. Overall, trans-3-Chlorocyclobutanecarboxylic acid is of interest in organic synthesis and may have applications in pharmaceuticals or agrochemicals due to its structural features.
Formula:C5H7ClO2
InChI:InChI=1/C5H7ClO2/c6-4-1-3(2-4)5(7)8/h3-4H,1-2H2,(H,7,8)/t3-,4-
SMILES:C1[C@@H](C[C@H]1Cl)C(=O)O
Synonyms:
  • Cyclobutanecarboxylic Acid, 3-Chloro-, Trans-
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