791616-65-4 Usage
Description
R-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 organic compound that features two naphthalene rings, a phosphorus atom, and multiple hydroxyl and phenyl groups. As a phosphine oxide and a member of the dioxaphosphepin class, this compound likely possesses a distinctive structure and properties that could be advantageous for particular chemical and industrial applications.
Uses
As the provided materials do not specify the exact uses and applications of R-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, it is not possible to list its uses according to the materials. However, given its classification and chemical structure, it can be inferred that this compound may have potential applications in various fields such as pharmaceuticals, materials science, or as an intermediate in the synthesis of other complex organic molecules. Further research and information would be required to determine its specific uses and potential impacts in different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 791616-65-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,1,6,1 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 791616-65:
(8*7)+(7*9)+(6*1)+(5*6)+(4*1)+(3*6)+(2*6)+(1*5)=194
194 % 10 = 4
So 791616-65-4 is a valid CAS Registry Number.
791616-65-4Relevant articles and documents
Chiral phosphoric acid catalyzed asymmetric friedel-crafts alkylation of indoles with nitroolefins
Tang, Hong-Ying,Zhang, Zhong-Biao
experimental part, 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
Highly enantioselective organocatalytic Biginelli reaction
Chen, Xiao-Hua,Xu, Xiao-Ying,Liu, Hua,Cun, Lin-Feng,Gong, Liu-Zhu
, p. 14802 - 14803 (2008/02/09)
A series of binol- and H8-binol-based phosphoric acids have for the first time been evaluated for their ability to catalyze Biginelli reactions of aldehydes, thiourea or urea, and β-keto esters. A new chiral phosphoric acid, derived from 3,3′-d
