2241598-30-9 Usage
Description
(R)-N-((S)-(2-(dicyclohexylphosphanyl)phenyl)(naphthalen-1-yl)methyl)-2-methylpropane-2-sulfinamide is a complex sulfinamide compound characterized by its intricate molecular structure. It features a sulfinamide group, a naphthalen-1-yl, and a dicyclohexylphosphanylphenyl group attached to a 2-methylpropane-2-sulfinamide moiety. (R)-N-((S)-(2-(dicyclohexylphosphanyl)phenyl)(naphthalen-1-yl)methyl)-2-methylpropane-2-sulfinamide is likely to have pharmaceutical or biological applications, potentially serving as a chiral ligand or catalyst in asymmetric synthesis reactions due to its stereochemical properties. The presence of phosphanyl and sulfinamide groups suggests that it could be involved in mediating chemical reactions or biological processes in a specific and controlled manner.
Uses
Used in Pharmaceutical Industry:
(R)-N-((S)-(2-(dicyclohexylphosphanyl)phenyl)(naphthalen-1-yl)methyl)-2-methylpropane-2-sulfinamide is used as a chiral ligand or catalyst for its potential role in asymmetric synthesis reactions, which are crucial in the production of enantiomerically pure pharmaceutical compounds. Its unique structure allows for the creation of molecules with specific stereochemistry, which is essential for the activity, safety, and efficacy of many drugs.
Used in Chemical Synthesis:
In the field of chemical synthesis, (R)-N-((S)-(2-(dicyclohexylphosphanyl)phenyl)(naphthalen-1-yl)methyl)-2-methylpropane-2-sulfinamide is used as a catalyst to facilitate specific and controlled chemical reactions. Its phosphanyl and sulfinamide groups may enable the compound to mediate reactions with high selectivity, leading to the production of desired products with minimal side reactions or byproducts.
Used in Research and Development:
(R)-N-((S)-(2-(dicyclohexylphosphanyl)phenyl)(naphthalen-1-yl)methyl)-2-methylpropane-2-sulfinamide is also used in research and development for studying its potential applications in various fields. Its unique structure and properties make it an interesting candidate for exploring new reaction mechanisms, biological activities, and potential therapeutic uses. Researchers may utilize this compound to gain insights into the behavior of similar molecules and develop new strategies for drug design and chemical synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 2241598-30-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 2,2,4,1,5,9 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2241598-30:
(9*2)+(8*2)+(7*4)+(6*1)+(5*5)+(4*9)+(3*8)+(2*3)+(1*0)=159
159 % 10 = 9
So 2241598-30-9 is a valid CAS Registry Number.
2241598-30-9Relevant articles and documents
Palladium-Catalyzed Enantioselective Reductive Heck Reactions: Convenient Access to 3,3-Disubstituted 2,3-Dihydrobenzofuran
Zhang, Zhan-Ming,Xu, Bing,Qian, Yanyan,Wu, Lizuo,Wu, Yuanqi,Zhou, Lujia,Liu, Yu,Zhang, Junliang
, p. 10373 - 10377 (2018)
The first example of highly enantioselective intramolecular hydroarylation of allyl aryl ethers was realized by palladium-catalyzed reductive heck reactions utilizing a new chiral sulfinamide phosphine ligand (N-Me-XuPhos). N-Me-XuPhos can be easily prepared on gram scale from readily available starting materials in a one-pot synthesis approach. A series of optically active 2,3-dihydrobenzofurans bearing a quaternary stereocenter were obtained in good yields and with excellent enantioselectivities. The practicality of this reaction was validated in the straightforward synthesis of CB2 receptor agonists. Moreover, deuterium was efficiently incorporated into the products.
