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CAS 1523606-40-7

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Cyclobutaneacetic acid, 3-amino-, hydrochloride (1:1), trans-

Description:
Cyclobutaneacetic acid, 3-amino-, hydrochloride (1:1), trans- is a chemical compound characterized by its unique structure, which includes a cyclobutane ring and an acetic acid moiety with an amino group. This compound is typically encountered as a hydrochloride salt, indicating that it is protonated and exists in a stable ionic form. The trans configuration suggests that specific substituents on the cyclobutane ring are oriented in a way that minimizes steric hindrance, which can influence its reactivity and interactions. The presence of the amino group introduces basic properties, allowing for potential interactions with acids and other electrophiles. This compound may exhibit solubility in polar solvents due to the presence of both hydrophilic (amino and carboxylic acid) and hydrophobic (cyclobutane) components. Its applications may span various fields, including pharmaceuticals and organic synthesis, where it could serve as an intermediate or a building block for more complex molecules. As with many chemical substances, safety and handling precautions should be observed due to potential biological activity or reactivity.
Formula:C6H11NO2·ClH
InChI:InChI=1/C6H11NO2.ClH/c7-5-1-4(2-5)3-6(8)9;/h4-5H,1-3,7H2,(H,8,9);1H/t4-,5-;
InChI key:InChIKey=VULUUIGASJOBOK-BPNVWSNHNA-N
SMILES:C(C(O)=O)[C@H]1C[C@H](N)C1.Cl
Synonyms:
  • Cyclobutaneacetic acid, 3-amino-, hydrochloride (1:1), trans-
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