(S)-3,3’-Bis(phenyl)-1,1’-bi-2-naphthol

≥98%,99%e.e.

Reagent Code: #65625
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CAS Number 102490-05-1

science Other reagents with same CAS 102490-05-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 438.5 g/mol
Formula C₃₂H₂₂O₂
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

(S)-3,3’-Bis(phenyl)-1,1’-bi-2-naphthol is widely used as a chiral ligand in asymmetric synthesis. It plays a crucial role in catalyzing enantioselective reactions, such as hydrogenation, alkylation, and Diels-Alder reactions, enabling the production of chiral compounds with high enantiomeric purity. This compound is particularly valuable in the pharmaceutical industry for synthesizing enantiomerically pure drugs, where the specific chirality can significantly impact the drug's efficacy and safety. Additionally, it is employed in the development of chiral catalysts and materials for organic electronics, contributing to advancements in optoelectronic devices and sensors. Its robust chiral framework also makes it useful in analytical chemistry for chiral separation techniques, aiding in the resolution of racemic mixtures.

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Test Parameter Specification
Appearance Off-White Powder
Purity (%) 98-100
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,915.00

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(S)-3,3’-Bis(phenyl)-1,1’-bi-2-naphthol
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(S)-3,3’-Bis(phenyl)-1,1’-bi-2-naphthol is widely used as a chiral ligand in asymmetric synthesis. It plays a crucial role in catalyzing enantioselective reactions, such as hydrogenation, alkylation, and Diels-Alder reactions, enabling the production of chiral compounds with high enantiomeric purity. This compound is particularly valuable in the pharmaceutical industry for synthesizing enantiomerically pure drugs, where the specific chirality can significantly impact the drug's efficacy and safety. Addit

(S)-3,3’-Bis(phenyl)-1,1’-bi-2-naphthol is widely used as a chiral ligand in asymmetric synthesis. It plays a crucial role in catalyzing enantioselective reactions, such as hydrogenation, alkylation, and Diels-Alder reactions, enabling the production of chiral compounds with high enantiomeric purity. This compound is particularly valuable in the pharmaceutical industry for synthesizing enantiomerically pure drugs, where the specific chirality can significantly impact the drug's efficacy and safety. Additionally, it is employed in the development of chiral catalysts and materials for organic electronics, contributing to advancements in optoelectronic devices and sensors. Its robust chiral framework also makes it useful in analytical chemistry for chiral separation techniques, aiding in the resolution of racemic mixtures.

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