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Chemodex
(1R)-(-)-Nopol
As low as
58
CHF
CHF 58.00
In stock
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CDX-N0658-G05050 gCHF 58.00
CDX-N0658-G100100 gCHF 90.00
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| Product Details | |
|---|---|
| Synonyms | (1R)-Nopol; (-)-Nopol; NSC1284; 6,6-Dimethyl-2-norpinen-2-ethanol; (1R)-6,6-Dimethylbicyclo[3.1.1]hept-2-ene-2-ethanol |
| Product Type | Chemical |
| Properties | |
| Formula | C11H18O |
| MW | 166.26 |
| CAS | 35836-73-8 |
| RTECS | RC8870000 |
| Source/Host Chemicals | Synthetic |
| Purity Chemicals | ≥98% (GC) |
| Appearance | Colourless viscous liquid. |
| Solubility | Slightly soluble in chloroform or MeOH. |
| Identity | Determined by 1H-NMR. |
| Declaration | Manufactured by Chemodex. |
| Other Product Data |
Click here for Original Manufacturer Product Datasheet |
| InChi Key | ROKSAUSPJGWCSM-UWVGGRQHSA-N |
| Smiles | OCCC1=CC[C@]2([H])C(C)(C)[C@@]1([H])C2 |
| Shipping and Handling | |
| Shipping | AMBIENT |
| Short Term Storage | +20°C |
| Long Term Storage | +20°C |
| Handling Advice | Protect from light and moisture. |
| Use/Stability | Stable for at least 2 years after receipt when stored at RT. |
| Documents | |
| Product Specification Sheet | |
| Datasheet |
 Download PDF |
Description
(1R)-Nopol is a chiral terpenol derivative, that can be used as a building block and intermediate for synthesis. Has been used in the preparation of optically active O,O-diterpenyl dithiophosphoric and O-terpenyl aryldithiophosphonic acids. Reacts 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. Can be used as a starting material for Pinaverium bromide, a selective gastrointestinal calcium ion antagonist used to treat irritable bowel syndrome. Due to its woody and minty aroma, Nopol is often used as a starting material for flavorings and fragrances. Gives a clean note for soaps and detergents.
Product References
(1) D.R. Arnold & X. Du; Can. J. Chem. 72, 403 (1994) | (2) M. Miyazawa, et al.; Phytochem. 39, 337 (1995) | (3) J.V. Crivello & S.S. Liu; J. Polymer Sci. Part A Polymer Chem. 37, 1199 (1999) | (4) L. Cointeaux, et al.; Tetrahedr. Lett. 43, 6275 (2002) | (5) E. Barriau, et al.; Macromolecules 41, 3779 (2008) | (6) R.A. Cherkasov, et al.; Phosph. Sulfur Relat. Elem. 186, 1003 (2011)