878111-16-1 Usage
Description
S-4-oxide-4-hydroxy-2,6-bis(4-nitrophenyl)-Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin is a complex chemical compound that belongs to the class of dioxaphosphepins. It features a phosphorus atom bonded to two oxygen atoms, along with two nitrophenyl groups and a dinaphtho skeleton. This highly functionalized and potentially reactive molecule is of interest in chemical synthesis and potential biological applications due to its unique properties.
Uses
Used in Chemical Synthesis:
S-4-oxide-4-hydroxy-2,6-bis(4-nitrophenyl)-Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin is used as a key intermediate in chemical synthesis for the development of new materials and compounds. Its unique structure and functional groups make it a valuable component in creating novel chemical entities.
Used in Pharmaceutical Development:
In the pharmaceutical industry, S-4-oxide-4-hydroxy-2,6-bis(4-nitrophenyl)-Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin is used as a starting material for the synthesis of potential drug candidates. Its hydroxy and nitro groups may offer unique properties that can be exploited for the development of new therapeutic agents.
Used in Material Science:
S-4-oxide-4-hydroxy-2,6-bis(4-nitrophenyl)-Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin is utilized in material science for the exploration of its potential in creating new materials with specific properties. Its complex molecular structure and functional groups may contribute to the development of advanced materials for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 878111-16-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,8,1,1 and 1 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 878111-16:
(8*8)+(7*7)+(6*8)+(5*1)+(4*1)+(3*1)+(2*1)+(1*6)=181
181 % 10 = 1
So 878111-16-1 is a valid CAS Registry Number.
878111-16-1Relevant articles and documents
Synthesis of novel chiral phosphoric acid-bearing two acidic phenolic hydroxyl groups and its catalytic evaluation for enantioselective Friedel-Crafts alkylation of indoles and enones
Liu, Xiong-Li,Yu, Zhang-Biao,Pan, Bo-Wen,Chen, Lin,Feng, Ting-Ting,Zhou, Ying
, p. 628 - 634 (2015/03/30)
A novel chiral phosphoric acid catalyst bearing two acidic phenolic hydroxyl groups was synthesized. Its catalytic activity as a chiral Br?sted acid has been examined in the enantioselective Friedel-Crafts alkylation of indoles and enones as a model reaction. In comparison with the other chiral phosphoric acid catalysts, the reaction catalyzed by the novel chiral catalyst afforded the desired 3-substituted indoles in a higher enantioselectivity (up to 69% ee).
ASYMMETRIC-SYNTHESIS CATALYST BASED ON CHIRAL BROENSTED ACID AND METHOD OF ASYMMETRIC SYNTHESIS WITH THE CATALYST
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Page/Page column 24, (2010/11/08)
A compound usable as an asymmetric synthesis catalyst which can be easily synthesized without using any metal such as a lanthanoid group element; a method of asymmetric synthesis with the compound; and a chiral compound obtained by the asymmetric synthesis method. A Broensted acid is used as a catalyst in asymmetric synthesis, the chiral Broensted acid being represented by formula (1) below or formula (3) below. The asymmetric synthesis method employs the catalyst. Asymmetric synthesis with the catalyst gives a chiral compound.
