82105-88-2 Usage
Description
(4-Ethoxybenzyl)triphenylphosphonium Bromide is a white powder chemical compound that serves as a versatile reagent in organic synthesis and has applications in enhancing the transport of certain molecules across artificial membranes.
Uses
Used in Organic Synthesis:
(4-Ethoxybenzyl)triphenylphosphonium Bromide is used as a Wittig reagent for the synthesis of various organic compounds. It aids in the conversion of aldehydes and ketones into olefins, which are essential in the production of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (4-Ethoxybenzyl)triphenylphosphonium Bromide is used to enhance the transport of ionized chloraphenicol succinate across an artificial membrane. This application is crucial for improving the bioavailability and effectiveness of certain drugs, allowing for better drug delivery systems and potentially leading to more efficient treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 82105-88-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,1,0 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 82105-88:
(7*8)+(6*2)+(5*1)+(4*0)+(3*5)+(2*8)+(1*8)=112
112 % 10 = 2
So 82105-88-2 is a valid CAS Registry Number.
InChI:InChI=1/C27H26OP.BrH/c1-2-28-24-20-18-23(19-21-24)22-29(25-12-6-3-7-13-25,26-14-8-4-9-15-26)27-16-10-5-11-17-27;/h3-21H,2,22H2,1H3;1H/q+1;
82105-88-2Relevant articles and documents
Alkoxylated p-phenylenevinylene oligomers: Synthesis and spectroscopic and electrochemical properties
Ndayikengurukiye, Henri,Jacobs, Sven,Tachelet, Wim,Van Der Looy, Johan,Pollaris, Anne,Geise, Herman J.,Claeys, Magda,Kauffmann, Jean M.,Janietz, Silvia
, p. 13811 - 13828 (2007/10/03)
Twenty-one n-alkoxy substituted phenylenevinylene oligomers were synthesized, varying in size, number and position of the OR groups. IR,MS and solubility data are presented. NMR measurements provided the molecular structure as well as information about conformations and molecular dynamics. UV and of cyclic voltammetric data give correlations of chemical structure (number and position of OR substituents) with separate HOMO and LUMO energies.
