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| | Cyclohexanecarbonitrile Basic information |
| | Cyclohexanecarbonitrile Chemical Properties |
| Melting point | 11 °C (lit.) | | Boiling point | 75-76 °C/16 mmHg (lit.) | | density | 0.919 g/mL at 25 °C (lit.) | | refractive index | n20/D 1.4505(lit.) | | Fp | 149 °F | | storage temp. | Keep in dark place,Sealed in dry,Room Temperature | | form | liquid | | color | Colourless | | Henry's Law Constant | 7.3×10-1 mol/(m3Pa) at 25℃, Hilal et al. (2008) | | InChI | 1S/C7H11N/c8-6-7-4-2-1-3-5-7/h7H,1-5H2 | | InChIKey | VBWIZSYFQSOUFQ-UHFFFAOYSA-N | | SMILES | N#CC1CCCCC1 | | CAS DataBase Reference | 766-05-2(CAS DataBase Reference) | | NIST Chemistry Reference | Cyclohexanecarbonitrile(766-05-2) |
| Hazard Codes | T | | Risk Statements | 24/25-36/37/38-23/24/25 | | Safety Statements | 36/37-45-36/37/39-26-23 | | RIDADR | UN 3276 6.1/PG 3 | | WGK Germany | 3 | | RTECS | GU7280000 | | HazardClass | 6.1 | | PackingGroup | Ⅲ | | HS Code | 2926907090 | | Storage Class | 6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects | | Hazard Classifications | Acute Tox. 3 Oral |
| | Cyclohexanecarbonitrile Usage And Synthesis |
| Uses | Cyclohexanecarbonitrile was used as model substrate in rhodium-catalyzed direct ortho-arylation reactions of phenylazoles using arylboron reagents. It was used as probe in the synthesis of an asymmetric, C-magnesiated nitrile. | | Synthesis Reference(s) | Journal of the American Chemical Society, 93, p. 4318, 1971 DOI: 10.1021/ja00746a052
Tetrahedron Letters, 25, p. 3301, 1984 DOI: 10.1016/S0040-4039(01)81369-1
The Journal of Organic Chemistry, 54, p. 4476, 1989 DOI: 10.1021/jo00279a047 |
| | Cyclohexanecarbonitrile Preparation Products And Raw materials |
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