2241598-34-3

Basic information

• Product Name: (S)-N-((R)-(3,5-di-tert-butyl-4-methoxyphenyl)(2-(dicyclohexylphosphanyl)phenyl)methyl)-N,2-dimethylpropane-2-sulfinamide
• CAS NO: 2241598-34-3
• Molecular Weight: 639.967
• Mol File: 2241598-34-3.mol

Chemical Properties

• Boiling Point: 702.9±70.0 °C(Predicted)
• CAS DataBase Reference: (S)-N-((R)-(3,5-di-tert-butyl-4-methoxyphenyl)(2-(dicyclohexylphosphanyl)phenyl)methyl)-N,2-dimethylpropane-2-sulfinamide(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-N-((R)-(3,5-di-tert-butyl-4-methoxyphenyl)(2-(dicyclohexylphosphanyl)phenyl)methyl)-N,2-dimethylpropane-2-sulfinamide(2241598-34-3)
• EPA Substance Registry System: (S)-N-((R)-(3,5-di-tert-butyl-4-methoxyphenyl)(2-(dicyclohexylphosphanyl)phenyl)methyl)-N,2-dimethylpropane-2-sulfinamide(2241598-34-3)

Safety Data

• Hazardous Substances Data: 2241598-34-3(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
(S)-N-((R)-(3,5-di-tert-butyl-4-methoxyphenyl)(2-(dicyclohexylphosphanyl)phenyl)methyl)-N,2-dimethylpropane-2-sulfinamide is used as a chiral ligand for asymmetric synthesis, which is crucial in the development of enantiomerically pure drugs. (S)-N-((R)-(3,5-di-tert-butyl-4-methoxyphenyl)(2-(dicyclohexylphosphanyl)phenyl)methyl)-N,2-dimethylpropane-2-sulfinamide's unique structural features allow for the creation of pharmaceuticals with improved efficacy and reduced side effects.
Used in Materials Science:
In the field of materials science, (S)-N-((R)-(3,5-di-tert-butyl-4-methoxyphenyl)(2-(dicyclohexylphosphanyl)phenyl)methyl)-N,2-dimethylpropane-2-sulfinamide can be utilized in the development of novel materials with specific properties, such as improved stability or reactivity, due to its unique molecular structure.
Used in Organic Chemistry Research:
(S)-N-((R)-(3,5-di-tert-butyl-4-methoxyphenyl)(2-(dicyclohexylphosphanyl)phenyl)methyl)-N,2-dimethylpropane-2-sulfinamide serves as a valuable compound in organic chemistry research, where it can be employed in the synthesis of complex organic molecules and the study of reaction mechanisms, further expanding the understanding of organic chemistry and its applications.

Upstream product

• 333-27-7 methyl trifluoromethanesulfonate 
• 108756-88-3 (dicyclohexylphosphino)borane 
• 583-53-9 2,3-dibromobenzene 
• 74684-38-1 2-(3-(tert-butyl)-5-formylphenyl)-2-methylpropanenitrile 
• 829-84-5 dicyclohexylphosphane 
• 74-88-4 methyl iodide 
• 1383686-30-3 (2-bromophenyl)-dicyclohexylphosphine borane 

Relevant articles and documents

Sequential Pd0- and PdII-Catalyzed Cyclizations: Enantioselective Heck and Nucleopalladation Reactions

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