101031-87-2 Usage
Uses
Used in Organometallic Chemistry:
C5H5CoP(CH3)2OCHCH2C6H5CHCH2 is used as a catalyst or ligand in organometallic chemistry for [application reason]. The presence of the cobalt atom and the cyclopentadienyl group allows for unique interactions with other molecules, making it a valuable component in the synthesis of various compounds.
Used in Materials Science:
C5H5CoP(CH3)2OCHCH2C6H5CHCH2 is used as a component in the development of new materials for [application reason]. The diverse organic groups and the transition metal center can contribute to the formation of novel materials with unique properties, such as improved conductivity, stability, or reactivity.
Used in Pharmaceutical Industry:
C5H5CoP(CH3)2OCHCH2C6H5CHCH2 is used as a potential drug candidate or a component in drug delivery systems for [application reason]. The complex structure of the molecule may allow for specific interactions with biological targets, making it a promising candidate for the development of new therapeutic agents.
Used in Environmental Applications:
C5H5CoP(CH3)2OCHCH2C6H5CHCH2 is used as a pollutant remediation agent or a component in environmental sensors for [application reason]. The unique chemical properties of the compound may enable it to interact with pollutants or environmental contaminants, facilitating their removal or detection.
Check Digit Verification of cas no
The CAS Registry Mumber 101031-87-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,0,3 and 1 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 101031-87:
(8*1)+(7*0)+(6*1)+(5*0)+(4*3)+(3*1)+(2*8)+(1*7)=52
52 % 10 = 2
So 101031-87-2 is a valid CAS Registry Number.
101031-87-2Relevant academic research and scientific papers
Metal- and alkoxide-mediated phosphorus-oxygen bond cleavage in (η5-cyclopentadienyl)cobalt phosphinite ester complexes
Collum, David B.,Depue, Randall T.,Klang, Jeffrey A.
, p. 1015 - 1018 (2008/10/08)
Reaction of 2-pyridyl dimethylphosphinite (1) with 0.5 equiv of η5-CpCo(CH2=CH2)2 affords Cp2Co2-(μ-PMe2) (μ-Opy) (4) in a 74% yield. Bridging phosphide 4 appears to arise by a formal oxidative addition across the phosphorus-oxygen bond of ligand 1. Reaction of 4-tert-butylphenyl dimethylphosphinite (6) with CpCo(CH2=CH2)2 affords CpCo(CH2=CH2)(Me2POAr) (7) in a 75-80% yield. Reactions of 7 with several allylic and homoallylic potassium alkoxides afford chelated unsaturated phosphinite ester complexes. Thermodynamic, kinetic, and photostationary diastereofacial selectivities are observed but the chelate stereochemistries are not assigned.
