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Usage

Uses

Used in Organic Light-Emitting Diode (OLED) Manufacturing:
R-3,3'-Bis(3,5-bis(methyl)phenyl)-1,1'-binaphthyl-2,2'-diyl hydrogenphosphate is used as a host material in OLED devices for its high photoluminescence efficiency. It helps improve the performance and stability of OLEDs, making it a crucial component in the manufacturing process.
Used in Electronic Devices:
Due to its high thermal and chemical stability, R-3,3'-Bis(3,5-bis(methyl)phenyl)-1,1'-binaphthyl-2,2'-diyl hydrogenphosphate is utilized in various electronic devices to ensure their durability and reliability. Its unique properties contribute to the overall performance and longevity of these devices.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, the compound's high chemical stability and unique structure may also make it a potential candidate for use in the pharmaceutical industry, possibly as a starting material for the synthesis of pharmaceutical compounds or as a component in drug delivery systems.
Used in Chemical Research:
R-3,3'-Bis(3,5-bis(methyl)phenyl)-1,1'-binaphthyl-2,2'-diyl hydrogenphosphate's unique properties and high stability may also make it valuable in chemical research, where it can be used to study the effects of various chemical reactions and processes on its structure and properties, potentially leading to new discoveries and applications.

Upstream product

• 75714-60-2 (S)-3-bromo-1-(3-bromo-2-methoxynaphthalen-1-yl)-2-methoxynaphthalene 
• 75640-87-8 (S)-2,2'-dimethoxy-1,1'-dinaphthyl 
• 215433-51-5 (S)-3,3’-bis(3,5-dimethylphenyl)-[1,1‘-binaphthalene]-2,2’-diol 

Relevant academic research and scientific papers

Organocatalytic asymmetric synthesis of propargylamines with two adjacent stereocenters: Mannich-type reactions of in situ generated C-alkynyl imines with β-keto esters

Side by side: The title reaction is catalyzed by the chiral Bronsted acid (S)-1, and affords hitherto less accessible chiral propargylamines, having two adjacent stereocenters, in good to excellent diastereo- and enantioselectivities. Boc=tert-butoxycarbonyl. Copyright

RETRACTED ARTICLE: Enantioselective organocatalytic hantzsch synthesis of polyhydroquinolines

The four-component Hantzsch reaction provides access to pharmaceutically important dihydropyridines. To expand the utility of this method, we have developed a route under organocatalytic conditions with good yields and excellent ee's. Through catalyst scr

Chiral lithium salts of phosphoric acids as Lewis acid-base conjugate catalysts for the enantioselective cyanosilylation of ketones

The catalytic enantioselective cyanosilylation of aromatic ketones was developed by using chiral lithium salts of (R)-BINOL- or (S)-BINAM-derived phosphoric acid compounds. In the presence of 10 mol% of chiral conjugate lithium salts, the corresponding tertiary cyanohydrins were obtained in high yields with moderate to high enantio-selectivities. This is the first efficient example of asymmetric catalysis using lithium salts of synthetically useful chiral phosphoric acid compounds. A possible catalytic mechanism and transition states are also discussed as a preliminary working hypothesis.