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| | (1R)-(-)-Nopol Basic information |
| Product Name: | (1R)-(-)-Nopol | | Synonyms: | (1R)-6,6-DIMETHYLBICYCLO[3.1.1]HEPT-2-ENE-2-ETHANOL;Dimethylbicyclohepteneethanol;(1R)-6,6-dimethylbicyclo[3.1.1]hept-2-en-2-ethanol;6,6-DIMETHYLBICYCLO(3.1.1)HEPT-2-ENE-2-ETHANOL;6,6-DIMETHYL-2-NORPINENE-2-ETHANOL;Bicyclo3.1.1hept-2-ene-2-ethanol, 6,6-dimethyl-, (1R,5S)-;(-)-Nopol, (1R)-6,6-Dimethylbicyclo[3.1.1]hept-2-ene-2-ethanol, 6,6-Dimethyl-2-norpinene-2-ethanol, 6,6-Dimethylbicyclo[3.1.1]hept-2-ene-2-ethanol;(1R)-6,6-Dimethylbicyclo[3.1.1]hept-2-ene-2-ethanol, 6,6-Dimethyl-2-norpinene-2-ethanol | | CAS: | 35836-73-8 | | MF: | C11H18O | | MW: | 166.26 | | EINECS: | 252-744-2 | | Product Categories: | | | Mol File: | 35836-73-8.mol |  |
| | (1R)-(-)-Nopol Chemical Properties |
| Boiling point | 235-236 °C(lit.) | | density | 0.973 g/mL at 25 °C(lit.) | | vapor pressure | 2.17Pa at 20℃ | | refractive index | n20/D 1.493 | | Fp | 210 °F | | storage temp. | Refrigerator, under inert atmosphere | | solubility | Chloroform (Slightly), Methanol (Slightly) | | pka | 15.03±0.10(Predicted) | | form | Oil | | color | Clear Colourless | | optical activity | [α]24/D 37°, neat | | Water Solubility | 333.5mg/L at 20℃ | | Merck | 14,6683 | | BRN | 3196379 | | LogP | 3.09 at 30℃ |
| Hazard Codes | Xn | | Risk Statements | 22-36/37/38 | | Safety Statements | 26-37/39 | | WGK Germany | 3 | | RTECS | RC8870000 | | HS Code | 29061900 |
| | (1R)-(-)-Nopol Usage And Synthesis |
| Chemical Properties | Clear colorless to light yellow liquid | | Uses | (-)-Nopol, is a chiral building block used in chemical synthesis. It is an intermediate that can be used for the synthesis of bulky moiety-modified analogs to the sandalwood odorant Polysantol. | | Definition | ChEBI: (-)-Nopol is a monoterpenoid. | | Application | (1R)-(-)-Nopol may be used in the preparation of optically active O,O-diterpenyl dithiophosphoric and O-terpenyl aryldithiophosphonic acids by reacting with tetraphosphorus decasulfide and 2,4-diaryl 1,3,2,4-dithiadiphosphetane-2,4-disulfides, respectively. It may also react with silver hexafluoroantimonate to form a complex, which can be an effective initiator for the nonthermal curing of epoxy resins by electron beam induced cationic polymerization. | | General Description | (1R)-(-)-Nopol is a chiral terpenol derivative. |
| | (1R)-(-)-Nopol Preparation Products And Raw materials |
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