
CAS 142733-63-9
:methyl cis-3-(boc-amino)cyclobutanecarboxylate
Description:
Methyl cis-3-(Boc-amino)cyclobutanecarboxylate is a chemical compound characterized by its cyclobutane ring structure, which is a four-membered carbon ring. The presence of a Boc (tert-butyloxycarbonyl) protecting group indicates that this compound is likely used in peptide synthesis or other organic reactions where amine protection is necessary. The "cis" configuration suggests that the substituents on the cyclobutane are oriented on the same side, which can influence the compound's reactivity and steric interactions. The methyl ester functional group contributes to its solubility in organic solvents and may participate in esterification or hydrolysis reactions. This compound is typically utilized in synthetic organic chemistry, particularly in the development of pharmaceuticals or biologically active molecules. Its specific properties, such as melting point, boiling point, and reactivity, would depend on the overall molecular structure and the presence of functional groups. Safety data and handling precautions should be consulted due to potential hazards associated with chemical synthesis and reactivity.
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Found 3 products.
Methyl cis-3-(Boc-amino)cyclobutanecarboxylate
CAS:Formula:C11H19NO4Purity:97%Color and Shape:SolidMolecular weight:229.2729Methyl cis-3-(Boc-amino)cyclobutanecarboxylate
CAS:<p>Methyl cis-3-(Boc-amino)cyclobutanecarboxylate</p>Formula:C11H19NO4Purity:≥95%Color and Shape: white powderMolecular weight:229.27g/mol


