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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 Chemical Structure of (1S,4S,5S)-4,7,7-Trimethyl-6-thiabicyclo[3.2.1]octane](/medias/Tci-440-T2579.jpg?context=bWFzdGVyfHJvb3R8MjkzMzd8aW1hZ2UvanBlZ3xhR1k1TDJnd055ODVNemc1TVRRNE1EUTFNelF5TDFSamFTMDBOREJmVkRJMU56a3VhbkJufDE1NTA3MmY1ZjNhMTliMDhhMGMxNzcwM2ZjYzgzMGM4ZjMxMjAxMzQwYzU2NjQ4YjgyMDY0OWViMWQxN2VmNzE) 
									 
							Purity: >98.0%(GC)
Synonyms:
						
						- (+)-Isothiocineole
Product Documents:
                    
				| Size | Unit Price | Same Day | 2-3 Business Days | Other Lead Time | Shipping Information   | 
|---|---|---|---|---|---|
| 1G | 
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| 5G | 
                                                $217.00 | 7 | 0 | Contact Us | 
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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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						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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![Thumbnail of (1S,4S,5S)-4,7,7-Trimethyl-6-thiabicyclo[3.2.1]octane](/medias/Tci-98-T2579.jpg?context=bWFzdGVyfHJvb3R8NDU3MXxpbWFnZS9qcGVnfGFHVTRMMmd3TkM4NU16ZzVNVFE0TVRFd09EYzRMMVJqYVMwNU9GOVVNalUzT1M1cWNHY3wwMTcxZmJjYmFiZTU0NDE0ZWZmN2MyNjRkMmYwZGZjZGI4OTQzZTFmNTUxN2I3YzdiYTA5NzFkOWYwYTJmOGVj)
![(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](/_ui/responsive/theme-tci/images/missing_product_zoom.jpg) 
       
	