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CAS RN: 247089-85-6 | Product Number: T2814
(R)-(-)-p-Toluenesulfinamide
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Purity: >98.0%(HPLC)
Synonyms:
Product Documents:
| Size | Unit Price | Hyderabad | Japan* | Quantity |
|---|---|---|---|---|
| 200MG |
₹4,300.00
|
3 | 3 |
|
| 1G |
₹15,400.00
|
3 | 9 |
|
*Upon orders receipt, Hyderabad stocks will be dispatched on the same day.
*Items available in Japan warehouse will be dispatched in 10-12 working days.
*INR price is exclusive of domestic taxes applicable.
*TCI frequently reviews storage conditions to optimize them. Please note that the latest information on the storage temperature for the products is described on our website.
| Product Number | T2814 |
Purity / Analysis Method 
|
>98.0%(HPLC) |
| Molecular Formula / Molecular Weight | C__7H__9NOS = 155.22 |
| Physical State (20 deg.C) | Solid |
| Storage Temperature
|
Room Temperature (Recommended in a cool and dark place, <15°C) |
| Packaging and Container
|
1G-Glass Bottle with Plastic Insert (View image), 200MG-Glass Bottle with Plastic Insert (View image) |
| CAS RN | 247089-85-6 |
| Reaxys Registry Number | 8110323 |
| PubChem Substance ID | 354334152 |
| MDL Number | MFCD06858374 |
Specifications
| Appearance | White to Orange to Green powder to crystal |
| Purity(HPLC) | min. 98.0 area% |
| Purity(with Total Nitrogen) | min. 97.0 % |
| Melting point | 116.0 to 120.0 °C |
| Specific rotation [a]20/D | -81.0 to -91.0 deg(C=1, CHCL3) |
Properties (reference)
| Melting Point | 118 °C |
| Specific Rotation | -86° (C=1,CHCl3) |
| Solubility (soluble in) | Methanol |
GHS
Related Laws:
Transport Information:
Application
Sufinamide for the Synthesis of Chiral Amines
Experimental procedure (1 to 2): In a flask equipped with argon is placed a solution of THF (100 mL) and NaHMDS (1.0 mol/L solution in THF, 148 mL, 148 mmol, 6 eq.) at -78 °C. Methyl acetate (7.85 mL, 98.8 mmol, 4 eq.) in THF (20 mL) is added slowly, and the solution is stirred for 1 h. At this time anhydrous ether (20 mL) and 1 (7.48 g, 24.7 mmol, 1 eq.) in THF (20 mL) are added. The reaction mixture is stirred at -78 °C for 3.5 h and quenched with sat. NH4Cl (50 mL). The solution is washed with ethyl acetate (3 x 150 mL), the organic phases are combined, dried (Na2SO4), and concentrated. Purification by flash chromatography (50% EtOAc/hexane) gives 2 (8.80 g, 85% yield) as an oil.
References
- Alkaloid Synthesis Using Chiral δ-Amino β-Ketoesters: A Stereoselective Synthesis of (－)-Lasubine II
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