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Home  > (11bS)-4-Hydroxy-2,6-bis(2,4,6-triisopropylphenyl)dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepine 4-oxide

AH92585

874948-63-7 | (11bS)-4-Hydroxy-2,6-bis(2,4,6-triisopropylphenyl)dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepine 4-oxide

Packsize Purity Availability Price Discounted Price    Quantity
100mg 98% +99%ee in stock $17.00 $12.00 -   +
250mg 98% +99%ee in stock $41.00 $29.00 -   +
1g 98% +99%ee in stock $162.00 $114.00 -   +
5g 98% +99%ee in stock $808.00 $566.00 -   +
10g 98% +99%ee in stock $1,397.00 $978.00 -   +

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*All prices are in USD.

Description
Catalog Number: AH92585
Chemical Name: (11bS)-4-Hydroxy-2,6-bis(2,4,6-triisopropylphenyl)dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepine 4-oxide
CAS Number: 874948-63-7
Molecular Formula: C50H57O4P
Molecular Weight: 752.9589
MDL Number: MFCD10567009
SMILES: CC(c1cc(cc(c1c1cc2ccccc2c2c1OP(=O)(O)Oc1c2c2ccccc2cc1c1c(cc(cc1C(C)C)C(C)C)C(C)C)C(C)C)C(C)C)C

 

Upstream Synthesis Route
  • The product "(11bS)-4-Hydroxy-2,6-bis(2,4,6-triisopropylphenyl)dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepine 4-oxide" serves as a versatile reagent in chemical synthesis. This compound, characterized by its unique structure containing a phosphorane oxide moiety and triisopropylphenyl groups, demonstrates remarkable reactivity and selectivity in a variety of synthetic transformations.In organic chemistry, this compound is commonly used as a catalyst or chiral ligand in asymmetric catalysis due to its ability to induce enantioselectivity in various reactions. For instance, it can facilitate asymmetric additions, cyclizations, and transformations of carbonyl compounds, olefins, and heteroatom nucleophiles with high efficiency and control. The chiral nature of the molecule plays a crucial role in governing the stereochemical outcomes of these reactions, leading to the formation of enantiomerically pure products.Additionally, the phosphorane oxide functionality in the molecule can participate in various nucleophilic substitution and cross-coupling reactions, providing a useful handle for further derivatization and functionalization of organic molecules. Its presence can enable the formation of new phosphorus-containing compounds or the modification of existing structures, thereby expanding the synthetic possibilities in organic chemistry.Overall, the application of "(11bS)-4-Hydroxy-2,6-bis(2,4,6-triisopropylphenyl)dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepine 4-oxide" in chemical synthesis showcases its significance as a valuable tool for designing and executing complex organic transformations with precision and control.
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