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(1-phenylcyclohexyl)methanamine
$360.00
CAS No.: 17380-54-0
Catalog No.: WLZ1881
Purity: 95%
MF: C13H19N
MW: 189.302
Storage: 2-8 degree Celsius
SMILES: C1(=CC=CC=C1)C1(CCCCC1)CN
Catalog No.: WLZ1881
Purity: 95%
MF: C13H19N
MW: 189.302
Storage: 2-8 degree Celsius
SMILES: C1(=CC=CC=C1)C1(CCCCC1)CN
For R&D use only. Not for human or animal use.
CAS NO.: 17380-54-0; (1-phenylcyclohexyl)methanamine. PROPERTIES: This cyclohexylamine derivative features a phenyl group attached to a cyclohexane ring connected to an amine group, creating a molecule with potential applications in organic synthesis and pharmaceutical research. The (1-phenylcyclohexyl)methanamine typically appears as a colorless to pale yellow liquid with moderate solubility in common organic solvents. Its molecular structure includes a cyclohexane ring that influences the electronic and steric properties of the molecule. For optimal stability and to prevent degradation, this compound should be stored at 2-8 degree Celsius in a tightly sealed container under anhydrous conditions. When handling, appropriate safety measures including nitrile gloves and safety goggles are essential. This compound is sensitive to moisture and may hydrolyze in aqueous environments. In case of accidental spillage, clean the area with a damp cloth and dispose of materials according to local regulations. APPLICATIONS: The (1-phenylcyclohexyl)methanamine serves as a versatile building block in organic synthesis, particularly for creating cyclohexyl-substituted amines. The amine group provides a handle for further functionalization through reactions such as acylation or alkylation. In medicinal chemistry, this compound functions as an intermediate for developing pharmaceuticals targeting enzyme inhibitors and receptor modulators. The phenyl substituent contributes to target binding affinity and selectivity. Additionally, the molecule finds utility in materials science as a monomer for creating polymers with specific electronic and optical properties. Researchers utilizing this compound benefit from its functional group versatility, enabling the development of diverse molecular architectures for applications ranging from drug discovery to advanced materials.
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