Cis-3-Aminocyclobutanemethanol is a cyclic amine with a unique structure that features a four-membered cyclobutane ring. This compound is characterized by the presence of an amino group and a hydroxymethyl group, which contribute to its reactivity and potential applications in organic synthesis and medicinal chemistry. The "cis" designation indicates that the amino and hydroxymethyl groups are positioned on the same side of the cyclobutane ring, influencing its stereochemistry and potentially its biological activity. The compound is typically a colorless to pale yellow liquid or solid, depending on its purity and form. Its molecular structure allows for hydrogen bonding, which can enhance solubility in polar solvents. Due to its functional groups, cis-3-Aminocyclobutanemethanol may exhibit properties such as being a potential building block for pharmaceuticals or other organic compounds. Additionally, its unique ring structure may impart specific conformational characteristics that could be relevant in drug design and development. As with many amines, it may also participate in various chemical reactions, including alkylation and acylation.

cis-3-Aminocyclobutanemethanol

142733-66-2: Cis-3-Aminocyclobutanemethanol is a cyclic amine with a unique structure that features a four-membered cyclobutane ring. This compound is characterized by the presence of an amino group and a hydroxymethyl group, which contribute to its reactivity and potential applications in organic synthesis and medicinal chemistry. The "cis" designation indicates that the amino and hydroxymethyl groups are positioned on the same side of the cyclobutane ring, influencing its stereochemistry and potentially its biological activity. The compound is typically a colorless to pale yellow liquid or solid, depending on its purity and form. Its molecular structure allows for hydrogen bonding, which can enhance solubility in polar solvents. Due to its functional groups, cis-3-Aminocyclobutanemethanol may exhibit properties such as being a potential building block for pharmaceuticals or other organic compounds. Additionally, its unique ring structure may impart specific conformational characteristics that could be relevant in drug design and development. As with many amines, it may also participate in various chemical reactions, including alkylation and acylation.

CAS 142733-66-2

cis-3-Aminocyclobutanemethanol

Cyclobutanemethanol,3-amino-,cis-(9CI)

Ref: IN-DA009JVD

(cis-3-Aminocyclobutyl)methanol

Ref: 10-F363484

cis-3-Aminocyclobutanemethan-1-ol HCl

Ref: 3D-SFA73366