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CAS 1638771-96-6

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Methyl cis-3-bromocyclobutanecarboxylate

Description:
Methyl cis-3-bromocyclobutanecarboxylate is an organic compound characterized by its cyclobutane ring structure, which is a four-membered carbon ring. The presence of a bromine atom at the 3-position of the cyclobutane ring introduces a halogen substituent, influencing the compound's reactivity and physical properties. The carboxylate functional group, specifically the methyl ester, contributes to its polar characteristics, enhancing solubility in polar solvents. This compound is likely to exhibit typical ester reactivity, including hydrolysis and transesterification. The cis configuration indicates that the bromine and the carboxylate group are on the same side of the cyclobutane ring, which can affect the compound's stereochemistry and potential interactions with biological systems. Methyl cis-3-bromocyclobutanecarboxylate may be of interest in synthetic organic chemistry, particularly in the development of pharmaceuticals or agrochemicals, due to its unique structural features and potential for further functionalization. Safety and handling precautions should be observed, as with all halogenated compounds, due to potential toxicity and environmental impact.
Formula:C6H9BrO2
InChI:InChI=1/C6H9BrO2/c1-9-6(8)4-2-5(7)3-4/h4-5H,2-3H2,1H3/t4-,5+
InChI key:InChIKey=PXUHGFNZFJXRFN-SYDPRGILNA-N
SMILES:C(OC)(=O)[C@@H]1C[C@H](Br)C1
Synonyms:
  • Methyl cis-3-bromocyclobutanecarboxylate
  • Cyclobutanecarboxylic acid, 3-bromo-, methyl ester, cis-
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