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Cyclohexylamine is used as an intermediate in synthesis of other organic compounds. It is the precursor to sulfenamide -based reagents used as accelerators for vulcanization. It is a building block for pharmaceuticals (e.g., mucolytics, analgesics, and bronchodilators ).
Jan 13, 2016 · 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. ChEBI. Cyclohexylamine is a natural product found in Phaseolus vulgaris and Zanthoxylum asiaticum with data available.
Cyclohexylamine. Formula: C 6 H 13 N. Molecular weight: 99.1741. IUPAC Standard InChI: InChI=1S/C6H13N/c7-6-4-2-1-3-5-6/h6H,1-5,7H2. IUPAC Standard InChIKey: PAFZNILMFXTMIY-UHFFFAOYSA-N. CAS Registry Number: 108-91-8. Chemical structure: This structure is also available as a 2d Mol file or as a computed 3d SD file.
CYCLOHEXYLAMINE is a clear to yellow liquid with an ammonia odor. It is highly flammable, corrosive, and toxic. Learn about its hazards, reactivity, firefighting, and response recommendations.
Molecular weight: 99.1741. IUPAC Standard InChI:InChI=1S/C6H13N/c7-6-4-2-1-3-5-6/h6H,1-5,7H2 Copy. IUPAC Standard InChIKey:PAFZNILMFXTMIY-UHFFFAOYSA-N Copy. CAS Registry Number: 108-91-8. 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 .
Find chapters and articles on cyclohexylamine, a secondary amine derived from cyclohexane, in various books and journals. Learn about its basicity, acidity, reaction kinetics, and applications in catalysis and organic chemistry.
cyclohexylamine. ChEBI ID. CHEBI:15773. Definition. A primary aliphatic amine consisting of cyclohexane carrying an amino substituent. Stars. This entity has been manually annotated by the ChEBI Team. Secondary ChEBI IDs. CHEBI:14054, CHEBI:23485, CHEBI:4017. Supplier Information. Download. Molfile XML SDF.
