60254-10-6 Usage
Description
(2-Hydroxyphenyl)diphenylphosphine is an organophosphorus compound characterized by its phosphine functional group and a hydroxyphenyl group attached to two phenyl rings. This unique structure endows it with versatile chemical properties and reactivity, making it a valuable compound in various synthetic and industrial applications.
Uses
Used in Catalyst Industry:
(2-Hydroxyphenyl)diphenylphosphine is used as a catalyst for the preparation of hydroxy(phosphinoxy)biphenyls, which are important intermediates in the synthesis of various pharmaceuticals and specialty chemicals. Its ability to facilitate selective reactions and improve product yields makes it a preferred choice in this application.
Used in Polymer Industry:
(2-Hydroxyphenyl)diphenylphosphine is used as a catalyst in the formation of ethylene copolymers, which are essential in the production of various plastics and materials with specific properties. Its catalytic activity helps in controlling the polymerization process, leading to copolymers with desired characteristics.
Used in Olefin Copolymerization:
(2-Hydroxyphenyl)diphenylphosphine is used as a catalyst for the copolymerization of ethylene with linear olefins, which is crucial in the manufacturing of polyethylene and other related polymers. Its role in this process ensures the formation of copolymers with tailored properties for specific end-use applications.
Used in Chemical Synthesis:
(2-Hydroxyphenyl)diphenylphosphine is used as a reagent in the silyation of aryl halides, a reaction that is important in the synthesis of various organic compounds, including pharmaceuticals and agrochemicals. Its ability to facilitate the formation of stable silylated products makes it a valuable tool in synthetic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 60254-10-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,2,5 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 60254-10:
(7*6)+(6*0)+(5*2)+(4*5)+(3*4)+(2*1)+(1*0)=86
86 % 10 = 6
So 60254-10-6 is a valid CAS Registry Number.
60254-10-6Relevant articles and documents
Synthesis and characterisation of the water soluble bis-phosphine complex [Ru(η6-cymene)(PPh2(o-C6H 4O)-κ2-P,O)(pta)]+ and an investigation of its cytotoxic effects
Renfrew, Anna K.,Egger, Alexander E.,Scopelliti, Rosario,Hartinger, Christian G.,Dyson, Paul J.
, p. 1144 - 1150 (2010)
Metal complexes bearing phosphine ligands are attracting increasing attention for their applications in medicinal chemistry. In particular, organometallic ruthenium-phosphine complexes have been found to exhibit promising antitumour activity. The synthesis, anticancer activity and reactivity of a novel bis-phosphine complex, [Ru(η6-cymene)(PPh 2(o-C6H4O)-κ2-P,O)(pta)]Cl (pta = 1,3,5-triaza-7-phosphatricyclo[3.3.1.1.]decane), is presented. The complex appears to exhibit its anticancer effect via a different mechanism to other ruthenium-arene pta complexes with labile co-ligands.
Electrophilic d0 Cations of Group 4 Metals (M = Ti, Zr, Hf) Derived from Monopentafulvene Complexes: Direct Formation of Tridentate Cp, O, P -Ligands
Fischer, Malte,Schaper, Raoul,Jaugstetter, Maximilian,Schmidtmann, Marc,Beckhaus, Rüdiger
supporting information, p. 1192 - 1205 (2018/04/17)
The reactions of the monopentafulvene complexes Ti1a and Ti1b with the general formula [CpTi(Cl)(π-η5:σ-η1-C5H4=CR2)] (R = p-tolyl (Ti1a); CR2 = adamantylidene (Ti1b)) with the bidentate P,
Aryl Fluorosulfate Trapped Staudinger Reduction
Ren, Gerui,Zheng, Qinheng,Wang, Hua
supporting information, p. 1582 - 1585 (2017/04/13)
A chemoselective Staudinger reduction/sulfur(VI) fluoride exchange cascade has been developed to join two chemical segments through an aryl sulfamate ester (RNH-SO2-OAr) linkage. Aryl fluorosulfate is exploited in this work as the first tetrahe
