945852-48-2 Usage
Description
S-4-oxide-8,9,10,11,12,13,14,15-octahydro-4-hydroxy-2,6-diphenyl-Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin is a complex chemical compound that features a unique structure with two naphthalene rings and a phosphorus-containing six-membered ring. This dioxaphosphepin derivative is enriched with hydroxy and phenyl groups, contributing to its intricate molecular architecture. The presence of phosphorus and oxygen in its composition suggests that it may exhibit notable chemical and potential biological activities, although the specific applications or effects are not explicitly mentioned in its nomenclature.
Uses
Used in Pharmaceutical Industry:
S-4-oxide-8,9,10,11,12,13,14,15-octahydro-4-hydroxy-2,6-diphenyl-Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin could be utilized as a pharmaceutical agent for the development of new drugs, given its complex structure and the presence of functional groups that may interact with biological targets.
Used in Chemical Research:
In the field of chemical research, this compound may serve as a subject for studying the synthesis of novel organic compounds, the exploration of its reactivity with other molecules, and the investigation of its potential as a catalyst or intermediate in chemical reactions.
Used in Material Science:
S-4-oxide-8,9,10,11,12,13,14,15-octahydro-4-hydroxy-2,6-diphenyl-Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin's unique structure and properties might make it a candidate for the development of new materials with specific characteristics, such as high thermal stability, unique electronic properties, or specific binding affinities.
Check Digit Verification of cas no
The CAS Registry Mumber 945852-48-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,5,8,5 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 945852-48:
(8*9)+(7*4)+(6*5)+(5*8)+(4*5)+(3*2)+(2*4)+(1*8)=212
212 % 10 = 2
So 945852-48-2 is a valid CAS Registry Number.
945852-48-2Relevant articles and documents
Chiral phosphoric acid catalyzed asymmetric friedel-crafts alkylation of indoles with nitroolefins
Tang, Hong-Ying,Zhang, Zhong-Biao
, p. 2038 - 2046 (2011/11/30)
Asymmetric Michael-type Friedel-Crafts (F-C) alkylations of indoles with nitroolefins catalyzed by a chiral H8-BINOL-based phosphoric acid were investigated. The reactions took place very smoothly in the presence of only 5 mol-% of catalyst at
Chiral Bronsted acid-catalyzed direct asymmetric Mannich reaction
Guo, Qi-Xiang,Liu, Hua,Guo, Chang,Luo, Shi-Wei,Gu, Yi,Gong, Liu-Zhu
, p. 3790 - 3791 (2008/02/03)
A chiral Bronsted acid-catalyzed direct asymmetric Mannich reaction has been described. Various phosphoric acids, prepared from BINOL and H8-BINOL derivatives, have been evaluated for catalyzing the direct Mannich reaction. In the presence of a
ASYMMETRIC-SYNTHESIS CATALYST BASED ON CHIRAL BROENSTED ACID AND METHOD OF ASYMMETRIC SYNTHESIS WITH THE CATALYST
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Page/Page column 30, (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.
