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| | (Aminomethyl)cyclohexane Basic information |
| | (Aminomethyl)cyclohexane Chemical Properties |
| Melting point | -8°C | | Boiling point | 159-161 °C (lit.) | | density | 0.87 g/mL at 25 °C (lit.) | | refractive index | n20/D 1.462(lit.) | | Fp | 110 °F | | form | Liquid | | pka | 10.42±0.29(Predicted) | | color | Clear colorless to slightly yellow | | Water Solubility | Slightly soluble in water. | | Sensitive | Air Sensitive | | BRN | 635751 | | CAS DataBase Reference | 3218-02-8(CAS DataBase Reference) | | NIST Chemistry Reference | c-C6H11CH2NH2(3218-02-8) |
| Hazard Codes | C | | Risk Statements | 10-34 | | Safety Statements | 16-26-36/37/39-45 | | RIDADR | UN 2734 8/PG 2 | | WGK Germany | 3 | | RTECS | GV6128000 | | HazardClass | 8 | | PackingGroup | II | | HS Code | 29213099 |
| | (Aminomethyl)cyclohexane Usage And Synthesis |
| Chemical Properties | Clear colorless to slightly yellow liquid | | Uses | Cyclohexanemethylamine was used in the synthesis of Schiff′s base ligand, 4-methyl-2,6-bis(cyclohexylmethyliminomethyl)-phenol, which forms hexanuclear zinc(II) complexes. Cyclohexanemethylamine was used during the synthesis of 1-acyl-4 cycloalkyl/arylsemicarbazides and 1-acyl-5-benzyloxy/hydroxyl carbamoylcarbazides from the nonsteroidal anti-inflammatory drugs. | | Synthesis Reference(s) | Tetrahedron Letters, 18, p. 2737, 1977 DOI: 10.1016/S0040-4039(01)83059-8
Synthesis, p. 441, 1981 DOI: 10.1055/s-1981-29473 |
| | (Aminomethyl)cyclohexane Preparation Products And Raw materials |
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