Antiseptics

Application Chiral resolving agent. Used in the synthesis of nonpeptide oxytocin antagonists.

(1 S )-(-)-Camphanic chloride is a chiral derivatizing agent . It can be prepared by reacting (-)-(1 S ,4 R )-camphanic acid with thionyl chloride.

(1 S )-(-)-Camphanic chloride is a chiral derivatizing agent . It can be prepared by reacting (-)-(1 S ,4 R )-camphanic acid with thionyl chloride.

(1S)-(-)-Camphor

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

Application (1 S , 2 S )-1,2-Bis(4-nitrophenyl)ethylenediamine dihydrochloride can be used to prepare a fluorous Fe-salen complex, which is used as a catalyst in the asymmetric epoxidation of C-C double bonds.

Application (1 S , 2 S )-1,2-di-1-Naphthyl-ethylenediamine dihydrochloride can be used to synthesize N , N &#8242-[(1 S ,2 S )-1,2-di-1-naphthyl-ethylene]bis2-propenamide, a chiral monomer, to prepare polymeric chiral stationary phase for HPLC.

(1 S ,2 R ,5 S )-(+)-menthol is a chiral secondary alcohol. Its alcohol group can be protected as 2-tetrahydrofuranyl ether by reacting with bromotrichloromethane and tetrahydrofuran.

(1 S ,2 R ,5 S )-(+)-menthol is a chiral secondary alcohol. Its alcohol group can be protected as 2-tetrahydrofuranyl ether by reacting with bromotrichloromethane and tetrahydrofuran.

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for catalytic efficiency.

(1S,2S)-(-)-N,N'-Dimethyl-1,2-bis[3-(trifluoromethyl)phenyl]ethylenediamine

(1S,2S)-1,2-Bis(2,4,6-trimethylphenyl)ethylenediamine dihydrochloride