Boc-(+/-)-trans-2-aminocyclohexanol is a chemical compound characterized by the presence of a Boc (tert-butyloxycarbonyl) protecting group attached to a trans-2-aminocyclohexanol structure. This compound features a cyclohexane ring with an amino group and a hydroxyl group, which are positioned in a trans configuration relative to each other. The Boc group serves as a protective moiety for the amino functionality, facilitating various synthetic applications, particularly in peptide synthesis and organic transformations. The compound is typically a white to off-white solid and is soluble in organic solvents such as dichloromethane and methanol, but may have limited solubility in water. Its chirality is indicated by the (+/-) designation, suggesting the presence of both enantiomers in the mixture. The compound is of interest in medicinal chemistry and organic synthesis due to its potential applications in drug development and as an intermediate in the synthesis of more complex molecules. Proper handling and storage conditions should be observed, as with many organic compounds, to ensure safety and stability.

Boc-(+/-)-trans-2-aminocyclohexanol

121282-70-0: trans-N-Boc-2-aminocyclohexanol

Tert-Butyl (trans-2-hydroxycyclohexyl)carbamate

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CAS 121282-70-0: Boc-(+/-)-trans-2-aminocyclohexanol

Boc-(+/-)-trans-2-aminocyclohexanol

Ref: IN-DA009D4J

Tert-Butyl (trans-2-hydroxycyclohexyl)carbamate

Ref: 10-F224672

tert-Butyl (trans-2-hydroxycyclohexyl)carbamate

Ref: 3D-FB140643