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| | 1,1-DIMETHOXYCYCLOHEXANE Basic information |
| Product Name: | 1,1-DIMETHOXYCYCLOHEXANE | | Synonyms: | 1,1-DIMETHOXYCYCLOHEXANE;Cyclohexanone dimethyl ketal 99%;TIMTEC-BB SBB008403;CYCLOHEXANONE DIMETHYL ACETAL;CYCLOHEXANONE DIMETHYL KETAL;DIMETHOXYCYCLOHEXANE;1,1-Dimethoxycyclohexane >;Cyclohexane, 1,1-dimethoxy- | | CAS: | 933-40-4 | | MF: | C8H16O2 | | MW: | 144.21 | | EINECS: | | | Product Categories: | | | Mol File: | 933-40-4.mol |  |
| | 1,1-DIMETHOXYCYCLOHEXANE Chemical Properties |
| Boiling point | 83 °C/50 mmHg (lit.) | | density | 0.948 g/mL at 25 °C (lit.) | | refractive index | n20/D 1.439(lit.) | | Fp | 50°C | | solubility | Chloroform (Soluble), Ethyl Acetate (Slightly) | | form | clear liquid | | color | Colorless to Yellow | | CAS DataBase Reference | 933-40-4(CAS DataBase Reference) |
| Risk Statements | 10-18 | | Safety Statements | 16-51 | | RIDADR | 3271 | | WGK Germany | 3 | | HS Code | 2911.00.5000 | | HazardClass | 3 | | PackingGroup | III |
| | 1,1-DIMETHOXYCYCLOHEXANE Usage And Synthesis |
| Uses | 1,1-Dimethoxycyclohexane is a useful research chemical used in the preparation of N-??substituted valiolamine derivatives as potential oral antidiabetic agents. | | Synthesis Reference(s) | Canadian Journal of Chemistry, 61, p. 366, 1983 DOI: 10.1139/v83-065
Tetrahedron Letters, 30, p. 6151, 1989 DOI: 10.1016/S0040-4039(01)93328-3 | | General Description | Cyclohexanone dimethyl ketal reacts with trimethylsilane in the presence of trimethylsilyl triflate to form the corresponding ether. It can also undergo allylation and propargylation in the presence of indium to form the corresponding homoallylic or homopropargylic alcohol, respectively. |
| | 1,1-DIMETHOXYCYCLOHEXANE Preparation Products And Raw materials |
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