26264-27-7 Usage
Uses
Used in Chemical Reactions:
(C6H5)3PBH2N(CH3)3+(PF6)-=(C6H5)3PBH2N(CH3)3PF6 is used as a reagent in various chemical reactions for its stability and high solubility in organic solvents, which allows for efficient participation in a wide range of synthetic processes.
Used in Pharmaceutical Industry:
(C6H5)3PBH2N(CH3)3+(PF6)-=(C6H5)3PBH2N(CH3)3PF6 is used as a starting material or intermediate in the synthesis of pharmaceutical compounds, taking advantage of its unique structural features and reactivity.
Used in Material Science:
(C6H5)3PBH2N(CH3)3+(PF6)-=(C6H5)3PBH2N(CH3)3PF6 is used in the development of new materials, such as organic conductors or advanced polymers, due to its potential to form complexes with various other molecules and ions.
Used in Analytical Chemistry:
(C6H5)3PBH2N(CH3)3+(PF6)-=(C6H5)3PBH2N(CH3)3PF6 can be employed as an ion-pairing agent in analytical chemistry, particularly in chromatographic techniques, to improve the separation and detection of certain compounds.
Used in Electrochemistry:
(C6H5)3PBH2N(CH3)3+(PF6)-=(C6H5)3PBH2N(CH3)3PF6 may be utilized in electrochemical applications, such as in the development of new electrolytes for batteries or supercapacitors, due to its ionic nature and stability.
Check Digit Verification of cas no
The CAS Registry Mumber 26264-27-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,2,6 and 4 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 26264-27:
(7*2)+(6*6)+(5*2)+(4*6)+(3*4)+(2*2)+(1*7)=107
107 % 10 = 7
So 26264-27-7 is a valid CAS Registry Number.
26264-27-7Relevant academic research and scientific papers
Smith, Gary L.,Kelly, Henry C.
, p. 2000 - 2004 (1969)
Salts containing bis(ligand)dihydroboron(1+) ions of the type LL′BH2+, where L and L′ are electron-donating ligands coordinated to boron through different group V or VI elements, including nitrogen, phosphorus, arsenic, and sulfur, have been prepared by displacement of halide ion from a (trialkyl donor)-haloborane adduct by the appropriate neutral ligand. Halide and hexafluorophosphate salts of the compounds have been characterized. The method is quite general for the preparation of a wide variety of boronium ions, as further illustrated by the synthesis of chelated boron(1+) ions and a dinuclear boron(2+) ion from the reaction of N,N,N′,N′-tetramethylethylenediamine with mono- and dihaloborane adducts of trimethylamine.
