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CAS RN: 1621994-95-3 | Product Number: M2765
(S)-3-[1-(4-Methoxybenzenesulfonyl)-(4S,5S)-4,5-diphenyl-4,5-dihydro-1H-imidazol-2-yl]-1,1'-binaphthalene-2,2'-diyl Hydrogen Phosphate
Purity: >96.0%(HPLC)
Synonyms:
Product Documents:
| Size | Unit Price | Saitama (Kawaguchi) | Hyogo (Amagasaki) | Stock in other WH |
Shipping Information
|
|---|---|---|---|---|---|
| 50MG |
¥34,800
|
15 | It can be shipped from Saitama warehouse on the same day* | Contact Us |
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* The displayed price is the unit price and does not include consumption tax. The unit prices displayed are the latest and are subject to change without notice.
* To send your quote request for bulk quantities, please click on the "Request Bulk Quote" button. Please note that we cannot offer bulk quantities for some products.
*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 | M2765 |
Purity / Analysis Method
|
>96.0%(HPLC) |
| Molecular Formula / Molecular Weight | C__4__2H__3__1N__2O__7PS = 738.75 |
| Physical State (20 deg.C) | Solid |
Storage Temperature
|
Frozen (<0°C) |
| Condition to Avoid | Heat Sensitive |
| CAS RN | 1621994-95-3 |
| Reaxys Registry Number | 27615196 |
| PubChem Substance ID | 354333322 |
Specifications
| Appearance | White to Yellow to Green powder to crystal |
| Purity(HPLC) | min. 96.0 area% |
| Elemental analysis(Nitrogen) | 3.50 to 4.00 % |
| Specific rotation [a]20/D | +275 to +295 deg(C=0.5, CHCl3) |
| NMR | confirm to structure |
Properties (reference)
| Melting Point | 205 °C(dec.) |
| Specific Rotation | 285° (C=0.5,CHCl3) |
GHS
Related Laws:
Transport Information:
Application
A Chiral Imidazoline-phosphoric Acid Catalyst Usable for the Desymmetrizating Reaction of meso-Aziridine Derivatives

Experimental procedure: The mixture of 1 (3.1 mg, 0.0042 mmol) and Ca(OMe)2 (0.4 mg, 0.0042 mmol) in methanol (0.08 mL) is stirred for 1 h. After removal of the solvent under reduced pressure, N-(2-pyridinesulfonyl)cyclohexaneaziridine (20.0 mg, 0.084 mmol) in toluene (1.68 mL) and molecular sieves 4Å (8.4 mg) are successively added, and the whole mixture is stirred at -20 °C. Then, trimethylsilylisothiocyanate (14.2 µL, 0.101 mmol) is added. After the disappearance of aziridine in the reaction mixture monitored by TLC, the water (3.0 mL) is added. The aqueous layer is extracted with CH2Cl2, the combined organic layer is dried over Na2SO4. Removal of solvent under reduced pressure gives the crude product, which is purified by flash chromatography on silica gel (hexane : ethyl acetate = 50 : 50) to afford the corresponding product as a white solid (24.8 mg, 88% ee) in 99% yield.
References
- Desymmetrization of meso-Aziridines with TMSNCS Using Metal Salts of Novel Chiral Imidazoline-Phosphoric Acid Catalysts
PubMed Literature
Documents
Product Articles
[Product Highlights] A Chiral Imidazoline-phosphoric Acid Catalyst Usable for the Desymmetrizating Reaction of meso-Aziridine DerivativesProduct Documents (Note: Some products will not have analytical charts available.)
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Specifications
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