text.skipToContent text.skipToNavigation

Maximum quantity allowed is 999

Please select the quantity

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:
50MG
$436.00
1   1   16  

* Items in stock locally ship in 1-2 business days. Items from Japan stock are able to ship from a US warehouse within 2 weeks. Please contact TCI for lead times on items not in stock. Excludes regulated items and items that ship on ice.
* To send your quote request for bulk quantities, please click on the "Request 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)
Properties (reference)
Melting Point 205 °C(dec.)
Specific Rotation 285° (C=0.5,CHCl3)
GHS
Related Laws:
Transport Information:
HS Number 2935.90.9500
Application
A Chiral Imidazoline-phosphoric Acid Catalyst Usable for the Desymmetrizating Reaction of meso-Aziridine Derivatives

M2765

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


PubMed Literature


Product Documents (Note: Some products will not have analytical charts available.)
Safety Data Sheet (SDS)
Please select Language.

The requested SDS is not available.

Please Contact Us for more information.

Specifications
C of A & Other Certificates
Please enter Lot Number Incorrect Lot Number. Please input only the 4-5 alphanumeric characters before the hyphen.

The product with the lot number searched for has been discontinued and no related documentation is available.

Sample C of A
This is a sample C of A and may not represent a recently manufactured lot of the product.

A sample C of A for this product is not available at this time.

Analytical Charts
Please enter Lot Number Incorrect Lot Number. Please input only the 4-5 alphanumeric characters before the hyphen.

The requested analytical chart is not available. Sorry for the inconvenience.

The product with the lot number searched for has been discontinued and no related documentation is available.

Other Documents

Session Status
Your session will timeout in 10 minutes. You will be redirected to the HOME page after session timeout. Please click the button to continue session from the same page. minute. You will be redirected to the HOME page after session timeout. Please click the button to continue session from the same page.

Your session has timed out. You will be redirected to the HOME page.