1054-59-7 Usage
General Description
The chemical "(diphenylphosphoryl-phenyl-phosphoryl)benzene" is a synthetic compound with the chemical formula C24H20O2P2. (diphenylphosphoryl-phenyl-phosphoryl)benzene is a type of organophosphorus compound, which are commonly used in pesticides, flame retardants, and other industrial applications. The chemical structure of "(diphenylphosphoryl-phenyl-phosphoryl)benzene" consists of two phenyl groups attached to a central benzene ring, with phosphoryl groups bonded to the phenyl groups. (diphenylphosphoryl-phenyl-phosphoryl)benzene may have potential uses in various chemical reactions and industrial processes due to its unique molecular structure and properties. However, it is important to handle and use compounds like "(diphenylphosphoryl-phenyl-phosphoryl)benzene" with caution, as organophosphorus compounds can be toxic and hazardous to human health and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 1054-59-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,5 and 4 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1054-59:
(6*1)+(5*0)+(4*5)+(3*4)+(2*5)+(1*9)=57
57 % 10 = 7
So 1054-59-7 is a valid CAS Registry Number.
InChI:InChI=1/C24H20O2P2/c25-27(21-13-5-1-6-14-21,22-15-7-2-8-16-22)28(26,23-17-9-3-10-18-23)24-19-11-4-12-20-24/h1-20H
1054-59-7Relevant articles and documents
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Spanier,Caropreso
, p. 199 (1969)
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Reaction of quinoline-5,8-diones with selected charged phosphorus nucleophiles
Nycz, Jacek E.,Malecki, Grzegorz,Chikkali, Samir,Hajdok, Imre,Singh, Priti
, p. 564 - 572 (2012)
The redox reactivity of the two quinoline-5,8-dione derivatives2-methyl-5, 8-dioxo-5,8-dihydroquinoline-7-amine (2a) and N-(2-methyl-5,8-dioxo-5,8- dihydroquinolin-7-yl)acet-amide (2b)has been demonstrated by their reaction with negatively charged three-c
New approaches to the synthesis of diphosphine dioxides and hypophosphoric acid esters
Nycz, Jacek E.,Musiol, Robert
, p. 310 - 316 (2007/10/03)
An union >P-O- has been applied as an efficient synthetic precursor of four coordination compounds of the R2P(O)-(O)PR 2 type, namely diphosphine dioxides (R = alkyl, aryl) as well as hypophosphoric acid esters (R = alkoxy, aryloxy), in a one-pot reaction. Furthermore, there were elaborated some mechanistic aspects of the origin of the >P(O)-O-(O)PP-O- and >P(O)X (X= Cl, Br) electrophiles. Attention is focused on the synthesis of the >P(O)-(O)P compounds.
Reactions of P_Cl compounds in presence of SMI2
Sasaki, Mitsuru,Collin, Jacqueline,Kagan, Henri B.
, p. 2493 - 2496 (2007/10/02)
Conversion of P-Cl to P-H and P-C bonds are induced by SmI2 in mild conditions. Especially phosphines oxides and sulfides are obtained in good yields.
