(11bS)​-8,​9,​10,​11,​12,​13,​14,​15-Octahydro-​4-​hydroxy-​2,​6-​bis[4-​(trifluoromethyl)​phenyl]​-4-​oxide-dinaphtho[2,​1-​d:1',​2'-​f]​[1,​3,​2]​dioxaphosphepin

≥98%,≥99%e.e.

  • Product Code: 70177
Molecular Weight: 644.5 g./mol Molecular Formula: C₃₄H₂₇F₆O₄P
EC Number: MDL Number:
Melting Point: Boiling Point:
Density: Storage Condition: room temperature, dry
Product Description: This compound is primarily utilized in advanced organic synthesis, particularly in the development of specialized catalysts and ligands. Its unique structure, featuring trifluoromethyl groups and a dioxaphosphepin ring, makes it highly effective in facilitating asymmetric reactions, which are crucial for producing enantiomerically pure compounds. These reactions are widely applied in the pharmaceutical industry to synthesize active pharmaceutical ingredients (APIs) with high precision and efficiency. Additionally, its stability and reactivity under various conditions make it a valuable component in the creation of novel materials, such as polymers and coatings, where specific chemical properties are required. The compound’s ability to act as a chiral inducer also finds applications in agrochemical research, aiding in the development of more effective and selective pesticides.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days $1,139.13
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(11bS)​-8,​9,​10,​11,​12,​13,​14,​15-Octahydro-​4-​hydroxy-​2,​6-​bis[4-​(trifluoromethyl)​phenyl]​-4-​oxide-dinaphtho[2,​1-​d:1',​2'-​f]​[1,​3,​2]​dioxaphosphepin
This compound is primarily utilized in advanced organic synthesis, particularly in the development of specialized catalysts and ligands. Its unique structure, featuring trifluoromethyl groups and a dioxaphosphepin ring, makes it highly effective in facilitating asymmetric reactions, which are crucial for producing enantiomerically pure compounds. These reactions are widely applied in the pharmaceutical industry to synthesize active pharmaceutical ingredients (APIs) with high precision and efficiency. Additionally, its stability and reactivity under various conditions make it a valuable component in the creation of novel materials, such as polymers and coatings, where specific chemical properties are required. The compound’s ability to act as a chiral inducer also finds applications in agrochemical research, aiding in the development of more effective and selective pesticides.
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