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CAS RN: 5718-75-2 | Product Number: T2578
(1R,4R,5R)-4,7,7-Trimethyl-6-thiabicyclo[3.2.1]octane
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![(1R,4R,5R)-4,7,7-Trimethyl-6-thiabicyclo[3.2.1]octane](/_ui/responsive/theme-tci/images/missing_product_zoom.jpg "(1R,4R,5R)-4,7,7-Trimethyl-6-thiabicyclo[3.2.1]octane")
Purity: >94.0%(GC)
Synonyms:
- (-)-Isothiocineole
Product Documents:
| Size | Unit Price | Same Day | 2-3 Business Days | Other Lead Time |
Shipping Information
|
|---|---|---|---|---|---|
| 1G |
$119.00
|
6 | 5 | It can be shipped in about 4-5 weeks after ordering | |
| 5G |
$450.00
|
6 | 0 | It can be shipped in about 4-5 weeks after ordering |
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* The storage conditions are subject to change without notice.
| Product Number | T2578 |
| Purity / Analysis Method | >94.0%(GC) |
| Molecular Formula / Molecular Weight | C__1__0H__1__8S = 170.31 |
| Physical State (20 deg.C) | Liquid |
| Storage Temperature | Room Temperature (Recommended in a cool and dark place, <15°C) |
| CAS RN | 5718-75-2 |
| Reaxys Registry Number | 80225 |
| PubChem Substance ID | 125307478 |
Specifications
| Appearance | Colorless to Almost colorless clear liquid |
| Purity(GC) | min. 94.0 % |
| Optical purity(GC) | min. 98.0 ee% |
Properties (reference)
| Boiling Point | 84 °C/5 mmHg |
| Flash point | 79 °C |
| Specific Gravity (20/20) | 1.00 |
| Specific Rotation | -70° (C=1.32,CHCl3) |
| Refractive Index | 1.52 |
GHS
| Signal Word | Warning |
| Hazard Statements | H227 : Combustible liquid. |
| Precautionary Statements | P501 : Dispose of contents/ container to an approved waste disposal plant. P210 : Keep away from heat/sparks/open flames/hot surfaces. No smoking. P280 : Wear protective gloves/ eye protection/ face protection. P370 + P378 : In case of fire: Use dry sand, dry chemical or alcohol-resistant foam to extinguish. P403 + P235 : Store in a well-ventilated place. Keep cool. |
Related Laws:
Transport Information:
| H.S.code* | 2934.99-000 |
Application
Chiral Sulfides for Optically Active Three-membered Rings
References
- 1) Practical and Highly Selective Sulfur Ylide Mediated Asymmetric Epoxidations and Aziridinations Using an Inexpensive, Readily Available Chiral Sulfide. Applications to the Synthesis of Quinine and Quinidine
- 2) Asymmetric synthesis of cyclopropyl phosphonates using chiral terpenyl sulfonium and selenonium ylidesw
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