957790-93-1

Basic information

• Product Name: (11bR)-2,6-bis[3,5-bis(1,1-diMethylethyl)-4-Methoxyphenyl]-4-hydroxy-4-oxide-Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin
• Synonyms: (11bR)-2,6-bis[3,5-bis(1,1-diMethylethyl)-4-Methoxyphenyl]-4-hydroxy-4-oxide-Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin;(R)-3,3'-Bis[3,5-bis(1,1-dimeth ylethyl)-4-methoxyphenyl]1,1' -binaphthyl-2,2'-diyl Hydrogen Phosphate
• CAS NO: 957790-93-1
• Molecular Formula: C50H57O6P
• Molecular Weight: 784.957741
• Mol File: 957790-93-1.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 860.7±75.0 °C(Predicted)
• Appearance: /
• Density: 1.21±0.1 g/cm3(Predicted)
• PKA: 1.12±0.20(Predicted)
• CAS DataBase Reference: (11bR)-2,6-bis[3,5-bis(1,1-diMethylethyl)-4-Methoxyphenyl]-4-hydroxy-4-oxide-Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin(CAS DataBase Reference)
• NIST Chemistry Reference: (11bR)-2,6-bis[3,5-bis(1,1-diMethylethyl)-4-Methoxyphenyl]-4-hydroxy-4-oxide-Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin(957790-93-1)
• EPA Substance Registry System: (11bR)-2,6-bis[3,5-bis(1,1-diMethylethyl)-4-Methoxyphenyl]-4-hydroxy-4-oxide-Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin(957790-93-1)

Safety Data

• Hazardous Substances Data: 957790-93-1(Hazardous Substances Data)

Usage

Description

(11bR)-2,6-bis[3,5-bis(1,1-diMethylethyl)-4-Methoxyphenyl]-4-hydroxy-4-oxide-Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin is a complex organic compound characterized by its unique molecular structure. It features two naphthalene rings connected by a dioxaphosphepin bridge, with multiple methyl, methoxy, and hydroxy groups attached to the aromatic rings. This highly sterically hindered diphosphine oxide is known for its distinctive properties and potential applications in various fields.

Uses

Used in Asymmetric Catalysis:
(11bR)-2,6-bis[3,5-bis(1,1-diMethylethyl)-4-Methoxyphenyl]-4-hydroxy-4-oxide-Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin serves as a valuable ligand in asymmetric catalysis, a branch of chemistry focused on the synthesis of enantiomerically pure compounds. Its unique steric and electronic properties enable the development of efficient and selective catalytic systems for a wide range of chemical reactions.
Used in Organometallic Chemistry:
(11bR)-2,6-bis[3,5-bis(1,1-diMethylethyl)-4-Methoxyphenyl]-4-hydroxy-4-oxide-Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin also finds application in organometallic chemistry, where it can act as a ligand for the formation of metal complexes. Its structural features allow for the fine-tuning of the electronic and steric properties of the resulting complexes, which can be employed in various catalytic processes and as precursors for the synthesis of advanced materials.
Used in the Development of New Chemical Processes:
The unique structure and properties of (11bR)-2,6-bis[3,5-bis(1,1-diMethylethyl)-4-Methoxyphenyl]-4-hydroxy-4-oxide-Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin make it a promising candidate for the development of innovative chemical processes. Its ability to act as a ligand in asymmetric catalysis and organometallic chemistry can lead to the discovery of new synthetic routes and the production of novel compounds with potential applications in various industries.
Used in the Synthesis of Advanced Materials:
(11bR)-2,6-bis[3,5-bis(1,1-diMethylethyl)-4-Methoxyphenyl]-4-hydroxy-4-oxide-Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin's distinctive features also make it a valuable building block for the synthesis of advanced materials with unique properties. Its potential use in the development of new materials can contribute to the advancement of various fields, such as pharmaceuticals, materials science, and nanotechnology, where innovative materials with specific characteristics are constantly sought after.