Cyclohexylamine - Wikipedia
Like other amines, it is a weak base, compared to strong bases such as NaOH, but it is a stronger base than its aromatic analog, aniline. It is a useful intermediate in the production of many other organic compounds (e.g. cyclamate)
Cyclohexylamine | C6H11NH2 | CID 7965 - PubChem
Cyclohexylamine is a primary aliphatic amine consisting of cyclohexane carrying an amino substituent. It has a role as a human xenobiotic metabolite and a mouse metabolite. It is a conjugate base of a cyclohexylammonium. Cyclohexylamine has been reported in Phaseolus vulgaris and Zanthoxylum asiaticum with data available. View More...
Cyclohexylamine - NIST Chemistry WebBook
Chemical structure: This structure is also available as a 2d Mol file or as a computed 3d SD file The 3d structure may be viewed using Java or Javascript. Permanent link for this species. Use this link for bookmarking this species for future reference.
Cyclohexylamine - (Organic Chemistry) - Vocab, Definition
Cyclohexylamine is an organic compound with the chemical formula C$_6$H$_{11}$NH$_2$. It is a primary amine derived from the cyclic hydrocarbon cyclohexane, and it exhibits the characteristic properties of aliphatic amines, including basicity and nucleophilicity.
Cyclohexylamine - NIST Chemistry WebBook
Follow the links above to find out more about the data in these sites and their terms of usage. The National Institute of Standards and Technology (NIST) uses its best efforts to deliver a high quality copy of the Database and to verify that the data contained therein have been selected on the basis of sound scientific judgment.
Cyclohexylamine - NIST Chemistry WebBook
Chemical structure: This structure is also available as a 2d Mol file or as a computed 3d SD file The 3d structure may be viewed using Java or Javascript. Permanent link for this species. Use this link for bookmarking this species for future reference.
Cyclohexylamine: Properties, Reactions, Production and Uses
Aug 14, 2024 · Cyclohexylamine is a weak base with a pKb of 3.4 that has similar reactivity of primary aliphatic amines. It forms salts with both Brønsted and Lewis acids. Exhaustive alkylation leads to quaternary ammonium cation formation. Cyclohexylamine reacts with carbon dioxide and carbon disulfide to produce carbamates and thiocarbamates, respectively.
Cyclohexylamine - an overview | ScienceDirect Topics
Explain the difference between the pK a values of the conjugate acids of the following bases. Answer: The smaller p K a of the conjugate acid of compound II means that it is the stronger acid. Thus, the second amine is the weaker base.
2.9: Organic Acids and Organic Bases - Chemistry LibreTexts
predict the relative acidity of two organic molecules from their structures. predict the relative basicity of two organic molecules from their structures. This page explains the acidity of simple organic acids and looks at the factors which affect their relative strengths.
Cyclohexylamine - chemeurope.com
Like other amines, it is of mildly alkaline nature, compared to strong bases such as NaOH, but it is a stronger base than its aromatic sister compound aniline, which differs only in that its ring is aromatic.