Cyclohexanol, 4-amino-1-methyl-, trans- is an organic compound characterized by a cyclohexanol structure with an amino group and a methyl group attached to the cyclohexane ring. The "trans" designation indicates the specific stereochemistry of the molecule, where the amino and methyl groups are positioned on opposite sides of the cyclohexane ring. This compound typically exhibits properties associated with alcohols, such as the ability to form hydrogen bonds, which can influence its solubility in water and other solvents. The presence of the amino group also suggests potential basicity and reactivity in various chemical reactions, including nucleophilic substitutions. Cyclohexanol derivatives are often used in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds, making them significant in both industrial and research contexts. The specific characteristics, such as boiling point, melting point, and reactivity, can vary based on the molecular structure and functional groups present, but detailed values would require specific experimental data.

Cyclohexanol, 4-amino-1-methyl-, trans-

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trans-4-Amino-1-methylcyclohexanol

Trans-4-Amino-1-methylcyclohexanol is a hydrogen-bonding molecule that can be synthesized by the reaction of an aldehyde and an amine. It has been shown to react with magnesium to form a Grignard reagent, which can then be used in other reactions such as bromination. Trans-4-Amino-1-methylcyclohexanol has two isomers, cis and trans, which are distinguished by the dihedral angle between their four substituents. The cis isomer has a dihedral angle of zero degrees while the trans isomer has a dihedral angle of 180 degrees. The x-ray structure for the cis isomer was determined and found to have two hydrogen bonds, one with water and one with ether.

CAS 177908-37-1: Cyclohexanol, 4-amino-1-methyl-, trans-

trans-4-Amino-1-methylcyclohexanol

Ref: 54-OR55239

Cyclohexanol, 4-amino-1-methyl-, trans-

Ref: IN-DA0025LC

Trans-4-Amino-1-methylcyclohexanol

Ref: 3D-FT171937