CAS 166168-16-7: trans-L-4-(Boc-aminomethyl)-cyclohexane methanamine

Description: Trans-L-4-(Boc-aminomethyl)-cyclohexane methanamine is a chemical compound characterized by its bicyclic structure, which includes a cyclohexane ring and an amine functional group. The "Boc" in its name refers to the tert-butyloxycarbonyl protecting group, commonly used in organic synthesis to protect amines during chemical reactions. This compound is typically utilized in the field of medicinal chemistry and peptide synthesis due to its ability to serve as a building block for more complex molecules. Its trans configuration indicates the specific spatial arrangement of substituents around the cyclohexane ring, which can influence its reactivity and interaction with biological targets. The presence of the methanamine group suggests that it has potential applications in drug development, particularly in the design of compounds that can interact with biological systems. Overall, this compound is significant in synthetic organic chemistry, particularly in the development of pharmaceuticals and biologically active molecules.

Formula: C₁₃H₂₆N₂O₂

InChI: InChI=1/C13H26N2O2/c1-13(2,3)17-12(16)15-9-11-6-4-10(8-14)5-7-11/h10-11H,4-9,14H2,1-3H3,(H,15,16)/t10-,11-

Synonyms:

• Tert-Butyl {[Trans-4-(Aminomethyl)Cyclohexyl]Methyl}Carbamate

Carbamic acid, N-[[trans-4-(aminomethyl)cyclohexyl]methyl]-, 1,1-dimethylethyl ester

CAS: 166168-16-7

• Formula: C₁₃H₂₆N₂O₂
• Purity: 95%
• Color and Shape: Liquid
• Molecular weight: 242.3577

trans-4-(Boc-Aminomethyl)-cyclohexanemethanamine

CAS: 166168-16-7

• Purity: 97%
• Color and Shape: Solid
• Molecular weight: 242.363

trans-4-(Boc-aminomethyl)cyclohexanemethanamine

CAS: 166168-16-7

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• Formula: C₁₃H₂₆N₂O₂
• Purity: Min. 95%
• Molecular weight: 242.36 g/mol