4-(Aminomethyl)cyclohexanone


Chemical Name: 4-(Aminomethyl)cyclohexanone
CAS Number: 934475-93-1
Product Number: AG00H5IC(AGN-PC-0WAIWS)
Synonyms:
MDL No:
Molecular Formula: C7H13NO
Molecular Weight: 127.1842

Identification/Properties


Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum


Other Analytical Data


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Chemical Structure



In chemical synthesis, 4-(Aminomethyl)cyclohexanone serves as a versatile building block that finds applications in various reactions and transformations. This compound contains a cyclohexanone ring with an aminoethyl group attached at the fourth carbon, imparting unique reactivity and functionality. One key application of 4-(Aminomethyl)cyclohexanone is in the synthesis of heterocyclic compounds. The aminoethyl group can undergo condensation reactions with carbonyl compounds or other reactive groups, leading to the formation of new ring systems. By utilizing the inherent reactivity of the amino group, diverse nitrogen-containing heterocycles can be synthesized, providing access to novel compounds with potentially valuable biological or pharmaceutical properties.Additionally, the presence of both an amine and a ketone functionality in 4-(Aminomethyl)cyclohexanone offers opportunities for further functionalization. The amine group can be involved in various transformations such as acylation, alkylation, or condensation reactions, allowing for the introduction of different substituents. The ketone moiety, on the other hand, can participate in reactions like reduction, oxidation, or nucleophilic addition, expanding the chemical versatility of the molecule.Overall, 4-(Aminomethyl)cyclohexanone plays a crucial role in chemical synthesis by enabling the construction of complex organic molecules through its reactivity and functional groups. Its applications in the development of heterocyclic compounds and the diversification of chemical structures highlight its significance as a valuable building block in organic synthesis.