220150-70-9 Usage
Uses
Used in Pharmaceutical Industry:
(1S,2S)-1,2-N,N'-BIS[(METHANE-SULFONYL)AMINO]-CYCLOHEXANE is used as a chiral resolving agent in chromatography for the production of enantiomerically pure drugs. It helps in separating the enantiomers of chiral compounds, which is crucial for the development of single-enantiomer drugs with desired therapeutic effects and reduced side effects.
Used in Organic Synthesis:
(1S,2S)-1,2-N,N'-BIS[(METHANE-SULFONYL)AMINO]-CYCLOHEXANE is used as a resolving agent for chiral amines in organic synthesis. It aids in obtaining enantiomerically pure amines, which are essential for the synthesis of various pharmaceuticals, agrochemicals, and other chiral molecules.
Used in Metal-Catalyzed Reactions:
(1S,2S)-1,2-N,N'-BIS[(METHANE-SULFONYL)AMINO]-CYCLOHEXANE can also be used as a ligand in metal-catalyzed reactions. Its chiral nature allows it to influence the stereochemistry of the reaction products, enabling the synthesis of enantiomerically enriched compounds.
Overall, (1S,2S)-1,2-N,N'-BIS[(METHANE-SULFONYL)AMINO]-CYCLOHEXANE is an important chemical compound with various applications in the field of organic chemistry and pharmaceuticals, particularly in the resolution of chiral compounds and the synthesis of enantiomerically pure products.
Check Digit Verification of cas no
The CAS Registry Mumber 220150-70-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,1,5 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 220150-70:
(8*2)+(7*2)+(6*0)+(5*1)+(4*5)+(3*0)+(2*7)+(1*0)=69
69 % 10 = 9
So 220150-70-9 is a valid CAS Registry Number.
220150-70-9Relevant academic research and scientific papers
Radi, Marco,Maga, Giovanni,Alongi, Maddalena,Angeli, Lucilla,Samuele, Alberta,Zanoli, Samantha,Bellucci, Luca,Tafi, Andrea,Casaluce, Gianni,Giorgi, Gianluca,Armand-Ugon, Mercedes,Gonzalez, Emmanuel,Este, José A.,Baltzinger, Mireille,Bec, Guillaume,Dumas, Philippe,Ennifar, Eric,Botta, Maurizio
, p. 840 - 851 (2009)
The role played by stereochemistry in the C2-substituent (left part) on the S-DABO scaffold for anti-HIV-1 activity has been investigated for the first time. A series of S-DABO analogues, where the double bond in the C2-substituent is replaced by an enant
