Product Description
Chemical name: 2-((2S,3S)-4-(Anthracen-9-yl)-3-(tert-butyl)-2,3-dihydrobenzo[d1,3]oxaphosphol-2-yl)pyridine
Synonyms: 2-((2S,3S)-4-(Anthracen-9-yl)-3-(tert-butyl)-2,3-dihydrobenzo[d1,3]oxaphosphol-2-yl)pyridine
2-((2S,3S)-4-(Anthracen-9-yl)-3-(tert-butyl)-2,3-dihydrobenzo[d1,3]oxaphosphol-2-yl)pyridine,97% (>99% ee)
Cas no: 2565792-34-7
Purity: 95%
Molecular formula: C30H26NOP
Molecular Weight:447.5
Appearance:SOLID Chiral Ligand for Advanced ResearchThis (S,S) enantiomeric phosphine oxide is a finely tuned reagent designed for applications in cutting-edge asymmetric synthesis and homogeneous catalysis. Its optically active center and complex aromatic framework provide selectivity and efficiency in developing novel chemical reactions, making it valuable in both academic and industrial laboratories.
Safe Handling and Storage RecommendationsGiven its slight sensitivity to moisture and light, the compound should be stored in a sealed container, under inert atmosphere, at 2-8C and protected from prolonged exposure to light. Personal protective equipment and a fume hood are essential during handling to prevent unintended exposure, ensuring safety throughout laboratory usage.
FAQ's of 2-((2S,3S)-4-(Anthracen-9-yl)-3-(tert-butyl)-2,3-dihydrobenzo[d][1,3] oxaphosphol-2-yl)pyridine:
Q: How should 2-((2S,3S)-4-(Anthracen-9-yl)-3-(tert-butyl)-2,3-dihydrobenzo[d][1,3]oxaphosphol-2-yl)pyridine be safely handled in the laboratory?
A: This compound should be handled with personal protective equipment, including gloves and eye protection, inside a fume hood. Direct contact with skin or eyes must be avoided, and all transfers should be conducted to minimize exposure to air and moisture.
Q: What is the primary usage of this chiral phosphine oxide compound?
A: It is primarily employed as a chiral ligand in homogeneous catalysis and asymmetric synthesis, facilitating the development of enantioselective reactions in chemical research and ligation studies.
Q: Where should I store this compound, and under what conditions?
A: The best storage conditions include keeping the solid at 2-8C (refrigerated), protected from light, in a tightly sealed container under an inert atmosphere to prevent moisture and light degradation.
Q: What benefits does the (S,S) enantiomeric form provide in research applications?
A: The optically pure (S,S) configuration grants selective interaction in chiral environments, thereby enabling enhanced control and efficiency in asymmetric synthesis and catalysis, which is crucial for creating enantiomerically pure products.
Q: When should spectral data or certificates of analysis be requested?
A: Spectral data such as NMR, HPLC, and MS can be requested from the supplier upon purchase or as needed to confirm quality, purity, and identity for specific research requirements.
Q: How is this product typically supplied and packaged?
A: It is usually distributed in small laboratory pack sizes (10 mg to 1 g) within sealed bottles or vials maintained under inert gas, ensuring stability during storage and transit.