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CAS RN: 1089663-51-3 | Product Number: T3080
N-(2-Thiophenesulfonyl)-L-prolinamide
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Purity: >98.0%(HPLC)
Synonyms:
Product Documents:
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| 100MG |
$119.00
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1 | 0 | It can be shipped in about 3-4 weeks after ordering |
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| Product Number | T3080 |
| Purity / Analysis Method | >98.0%(HPLC) |
| Molecular Formula / Molecular Weight | C__9H__1__2N__2O__3S__2 = 260.33 |
| Physical State (20 deg.C) | Solid |
| Storage Temperature | Room Temperature (Recommended in a cool and dark place, <15°C) |
| CAS RN | 1089663-51-3 |
| Reaxys Registry Number | 19412755 |
| PubChem Substance ID | 253661577 |
Specifications
| Appearance | White to Light yellow powder to crystal |
| Purity(HPLC) | min. 98.0 area% |
| Optical purity(LC) | min. 99.0 ee% |
| Elemental analysis(Nitrogen) | 10.30 to 11.00 % |
| NMR | confirm to structure |
Properties (reference)
GHS
Related Laws:
Transport Information:
| H.S.code* | 2935.90-000 |
Application
Prolinamide Catalyzing Asymmetric Aldol Reactions
Experimental procedure: 4,6-Dibromoisatin (25 mg, 0.082 mmol) is added to a mixture of N-(2-thiophenesulfonyl)-L-prolinamide TFA salt (1.5 mg, 0.004 mmol) and water (14 μL, 0.8 mmol) in acetone (1.2 mL, 16.4 mmol) at 0 °C. After stirring for 8 h, the solvent is removed under reduced pressure to give a residue that is purified by column chromatography (hexane:EtOAc = 1:1) to give (R)-convolutamydine (29.6 mg, 99%, 95% ee).
References
- Enantioselective Synthesis of (R)-Convolutamydine A with New N-Heteroarylsulfonylprolinamides
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