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CAS RN: 1208985-45-8 | Product Number: T2579
(1S,4S,5S)-4,7,7-Trimethyl-6-thiabicyclo[3.2.1]octane
![(1S,4S,5S)-4,7,7-Trimethyl-6-thiabicyclo[3.2.1]octane No-Image](/medias/Tci-440-T2579.jpg?context=bWFzdGVyfHJvb3R8MjkzMzd8aW1hZ2UvanBlZ3xhR1k1TDJnd055ODVNemc1TVRRNE1EUTFNelF5TDFSamFTMDBOREJmVkRJMU56a3VhbkJufDE1NTA3MmY1ZjNhMTliMDhhMGMxNzcwM2ZjYzgzMGM4ZjMxMjAxMzQwYzU2NjQ4YjgyMDY0OWViMWQxN2VmNzE)
Purity: >98.0%(GC)
Synonyms:
- (+)-Isothiocineole
Product Documents:
Size | Unit Price | Shanghai | Tianjin | Japan* |
---|---|---|---|---|
1G |
¥610.00
|
3 | 1 | 20 |
5G |
¥1,690.00
|
3 | 1 | 11 |
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Product Number | T2579 |
Purity / Analysis Method | >98.0%(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 | 1208985-45-8 |
Reaxys Registry Number | 105189 |
PubChem Substance ID | 125307479 |
Specifications
Appearance | Colorless to Almost colorless clear liquid |
Purity(GC) | min. 98.0 % |
Optical purity(GC) | min. 97.0 ee% |
NMR | confirm to structure |
Properties (reference)
Flash point | 79 °C |
Specific Rotation | 67° (neat) |
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. |
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Customs Control Conditions (Q) |
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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