223742-01-6 Usage
Description
(2-DICHLOROPHOSPHINOPHENYL)DIPHENYLPHOSPHINE is an organophosphorus compound that features a phosphinophenyl group and two phenyl groups bonded to a central phosphorus atom. It is recognized for its applications in organometallic chemistry and catalysis, where it serves as a versatile ligand. (2-DICHLOROPHOSPHINOPHENYL)DIPHENYLPHOSPHINE also holds promise as a component in the creation of innovative materials and pharmaceuticals, and it has been considered for its flame retardant properties due to its phosphorus content. However, it is imperative to handle this chemical with caution due to its potential hazards and toxicity.
Uses
Used in Organometallic Chemistry:
(2-DICHLOROPHOSPHINOPHENYL)DIPHENYLPHOSPHINE is used as a ligand to facilitate various chemical reactions in organometallic chemistry. Its unique structure allows it to bind with metal atoms, enhancing the reactivity and selectivity of the reactions.
Used in Catalysis:
In the field of catalysis, (2-DICHLOROPHOSPHINOPHENYL)DIPHENYLPHOSPHINE is employed as a ligand to improve the efficiency of catalytic processes. It plays a crucial role in the synthesis of a wide range of organic compounds, contributing to the advancement of chemical processes.
Used in Material Science:
(2-DICHLOROPHOSPHINOPHENYL)DIPHENYLPHOSPHINE is used as a building block in material science for the development of new materials. Its phosphorus-containing structure offers potential applications in creating novel materials with specific properties.
Used in Pharmaceutical Development:
(2-DICHLOROPHOSPHINOPHENYL)DIPHENYLPHOSPHINE is utilized in the pharmaceutical industry as a component in the development of new drugs. Its unique chemical properties make it a valuable candidate for the creation of innovative pharmaceuticals.
Used as a Flame Retardant:
Due to its phosphorus content, (2-DICHLOROPHOSPHINOPHENYL)DIPHENYLPHOSPHINE has been studied for its potential use as a flame retardant. It may be incorporated into materials to enhance their resistance to fire, thereby improving safety standards.
Used in Chemical Research:
In the realm of chemical research, (2-DICHLOROPHOSPHINOPHENYL)DIPHENYLPHOSPHINE serves as a subject of study for understanding its properties, reactivity, and potential applications in various chemical processes and industries.
Check Digit Verification of cas no
The CAS Registry Mumber 223742-01-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,3,7,4 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 223742-01:
(8*2)+(7*2)+(6*3)+(5*7)+(4*4)+(3*2)+(2*0)+(1*1)=106
106 % 10 = 6
So 223742-01-6 is a valid CAS Registry Number.
223742-01-6Relevant articles and documents
New chiral phosphine-phosphonites derived from (2R,3R)-dimethyl tartrate, (S)-binaphthol and (1R,2S)-ephedrine
Schull, Terence L.,Knight, D. Andrew
, p. 207 - 211 (1999)
The reaction of 2-lithiophenyldiphenylphosphine with phosphorus trichloride afforded the new unsymmetric phosphine, dichloro(2- diphenylphosphinophenyl)phosphine (4). Condensation of 4 with (a) (2R,3R)- dimethyl tartrate or (b) (S)-binaphthol in the prese
New non-C2-symmetric phosphine-phosphonites as ligands in asymmetric metal catalysis
Reetz, Manfred T.,Gosberg, Andreas
, p. 2129 - 2137 (2007/10/03)
Starting from 1,2-dibromobenzene, the synthesis of N,N,N',N'-tetraethyl-[2-(diphenylphosphino)phenyl]phosphonous acid tetraamide is possible in two simple steps. This key compound reacts with a variety of chiral diols such as (R)- and (S)-binaphthol, 1,2:5,6-diisopropylidene-D-mannitol or (1R,2R)-1,2-diphenyl-1,2-ethane diol to form the corresponding non-C2-symmetric phosphine-phosphonite compounds. These ligands react with Rh(COD)2BF4 to form bidentate Rh-complexes which serve as catalysts in the asymmetric hydrogenation of dimethyl itaconate with ee values of up to 88%.
