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Home  > 1,​1,​1-Trifluoro-​N-​[(11bR)​-​4-​oxido-​2,​6-​diphenyldinaphtho[2,​1-​d:1',​2'-​f]​[1,​3,​2]​dioxaphosphepin-​4-​yl]methanesulfonamide

AI67822

1010799-98-0 | 1,​1,​1-Trifluoro-​N-​[(11bR)​-​4-​oxido-​2,​6-​diphenyldinaphtho[2,​1-​d:1',​2'-​f]​[1,​3,​2]​dioxaphosphepin-​4-​yl]methanesulfonamide

Packsize Purity Availability Price Discounted Price    Quantity
50mg 97% in stock $129.00 $90.00 -   +
100mg 97% in stock $192.00 $135.00 -   +
250mg 97% in stock $306.00 $214.00 -   +
1g 97% in stock $760.00 $532.00 -   +

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Description
Catalog Number: AI67822
Chemical Name: 1,​1,​1-Trifluoro-​N-​[(11bR)​-​4-​oxido-​2,​6-​diphenyldinaphtho[2,​1-​d:1',​2'-​f]​[1,​3,​2]​dioxaphosphepin-​4-​yl]methanesulfonamide
CAS Number: 1010799-98-0
Molecular Formula: C33H21F3NO5PS
Molecular Weight: 631.5575
SMILES: C1=CC=C(C=C1)C2=CC3=CC=CC=C3C4=C2OP(=O)(OC5=C4C6=CC=CC=C6C=C5C7=CC=CC=C7)NS(=O)(=O)C(F)(F)F

 

Upstream Synthesis Route 
  • The compound 1,1,1-Trifluoro-N-[(11bR)-4-oxido-2,6-diphenyldinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl]methanesulfonamide is commonly utilized in chemical synthesis as a powerful reagent for various reactions. It serves as an important building block in the creation of complex organic molecules, particularly in the realm of medicinal and material chemistry. This compound's unique structural features enable it to participate in a wide range of transformations, including asymmetric catalysis, cross-coupling reactions, and heterocycle synthesis. Its remarkable reactivity and selective functional groups make it a valuable tool for organic chemists seeking to access novel structures and enhance synthetic efficiency.
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