34257-63-1 Usage
General Description
(N-METHYL-N-PHENYLAMINO)TRIPHENYLPHOSPHONIUM IODIDE is a chemical compound with the formula C25H24NPI. It is a triphenylphosphonium salt that contains a positively charged phosphonium ion and a negatively charged iodide ion. (N-METHYL-N-PHENYLAMINO)TRIPHENYLPHOSPHONIUM IODIDE is widely used in organic chemistry as a strong Lewis acid catalyst, especially in the synthesis of various organic compounds. It is also utilized in the manufacturing of pharmaceuticals and agrochemicals. Additionally, it is known for its antimicrobial and antifungal properties, making it a valuable ingredient in the production of disinfectants and preservatives. Overall, (N-METHYL-N-PHENYLAMINO)TRIPHENYLPHOSPHONIUM IODIDE is a versatile and important chemical in various industrial and scientific applications.
Check Digit Verification of cas no
The CAS Registry Mumber 34257-63-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,2,5 and 7 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 34257-63:
(7*3)+(6*4)+(5*2)+(4*5)+(3*7)+(2*6)+(1*3)=111
111 % 10 = 1
So 34257-63-1 is a valid CAS Registry Number.
InChI:InChI=1/C25H23NP.HI/c1-26(22-14-6-2-7-15-22)27(23-16-8-3-9-17-23,24-18-10-4-11-19-24)25-20-12-5-13-21-25;/h2-21H,1H3;1H/q+1;/p-1
34257-63-1Relevant articles and documents
PHOSPHORORGANISCHE VERBINDUNGEN 89 Quartaere Phosphoniumsalze mit Heteroatomen am Phosphor Herstellung, Eigenschaften und Elektroreduktive Spaltung
Horner, Leopold,Jordan, Manfred
, p. 209 - 214 (2007/10/02)
The half-potential of 35 quaternary phosphonium salts with one or more hetero-atoms attached to phosphorus are reported, and the fission products determined for the electroreduction of nine phosphonium salts.The influence of the ligands attached to phosphorus by hetero-atoms on both the half-wave potential and the course of the fission reaction is discussed.The order of precedence in the cleavage of the ligands at phosphorus is examined to determine whether a meaningful, qualitative order of stability for the corresponding ligands as free radicals can be deduced.
