24744-62-5 Usage
Uses
Used in Coordination Chemistry:
(2,2-dimethoxyethyl)(diphenyl)phosphane is utilized as a ligand in coordination chemistry, where it plays a crucial role in the formation and stabilization of metal complexes. Its presence enhances the stability and reactivity of these complexes, making it a valuable component in this field.
Used in Organometallic Catalysis:
In organometallic catalysis, (2,2-dimethoxyethyl)(diphenyl)phosphane serves as a ligand to modify the properties of catalysts, thereby improving their efficiency and selectivity in various chemical reactions. Its ability to fine-tune catalyst performance makes it an indispensable tool in this area.
Used in Pharmaceutical Synthesis:
(2,2-dimethoxyethyl)(diphenyl)phosphane is employed as a synthetic intermediate in the development of pharmaceuticals. Its unique structure and reactivity enable the creation of novel drug candidates with potential therapeutic applications.
Used in Materials Science:
In the field of materials science, (2,2-dimethoxyethyl)(diphenyl)phosphane is used in the development of new functional materials. Its incorporation into these materials can lead to enhanced properties, such as improved conductivity, stability, or specific interactions with other molecules.
Overall, (2,2-dimethoxyethyl)(diphenyl)phosphane is a multifaceted chemical with a wide range of applications across different industries, including coordination chemistry, organometallic catalysis, pharmaceuticals, and materials science. Its unique structure and reactivity make it a valuable asset in these fields.
Check Digit Verification of cas no
The CAS Registry Mumber 24744-62-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,7,4 and 4 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 24744-62:
(7*2)+(6*4)+(5*7)+(4*4)+(3*4)+(2*6)+(1*2)=115
115 % 10 = 5
So 24744-62-5 is a valid CAS Registry Number.
24744-62-5Relevant academic research and scientific papers
Synthesis, physicochemical analysis of two new hemilabile ether-phosphine ligands and their first stable bis-ether-phosphine/cobalt(II) tetrahedral complexes
Warad, Ismail,Barakat, Assem
, p. 17 - 24 (2017/01/03)
New tridentate ether-phosphine {P, 2O} and ether-phosphine oxide {OP, 2O} ligands with P and O donor-atoms have been synthesized starting from ClCH2CH(OCH3)2. The oxidation process of Ph2PCH2CH(OCH3)2 to its oxide derivative Ph2P([dbnd]O)CH2CH(OCH3)2 was monitored by 31P NMR for the first time. The desired ligands and their Co(II) complexes structures were deduced from IR, EA, MS, NMR, UV–Vis., TG/DTG and XRD physical measurements. The tridentate chelating coordination behavior of the ether-phosphine wasn't detected leading only to the mono-dentate coordination mode through the phosphorous atoms to set up a X2Co[η1-Ph2PCH2CH(OCH3)2]2 as final isomer formula (X?=?Cl or Br). The Cl2Co[η1-Ph2PCH2CH(OCH3)2]2 isomer belongs to complex 1 was supported by single crystal measurement. Polar/non-polar intermolecular short contacts were detected by XRD and Hirshfeld surface theoretical analysis.
Palladacycle mediated synthesis of cyano-functionalized chiral 1,2-diphosphine and subsequent functional group transformations
Yuan, Mingjun,Pullarkat, Sumod A.,Li, Yongxin,Leung, Pak-Hing
experimental part, p. 905 - 912 (2011/03/21)
Cyano-functionalized allylic phosphine substrates containing the ortho-metalated (R)-(1-(dimethylamino)ethyl)naphthalene as the chiral auxiliary were synthesized from bromoacetaldehyde dimethylacetal via a one-pot process. The diastereoselective hydrophos
