55552-25-5 Usage
Uses
Used in Pharmaceutical Industry:
(alpha-Ethoxyvinyl)triphenylphosphonium bromide is used as a reagent for the preparation of hydrazones and hydroxylamino phosphine oxides, which are important intermediates in the synthesis of various pharmaceutical compounds. Its ability to facilitate dehydrogenation, alkylation, and base hydrolysis of phosphonioalkyl-substituted hydrazines and hydroxylamines contributes to the development of novel drug candidates with potential therapeutic applications.
Used in Chemical Research:
In the field of chemical research, (alpha-ethoxyvinyl)triphenylphosphonium bromide serves as a valuable tool for exploring new reaction pathways and understanding the underlying mechanisms involved in the formation of complex organic molecules. Its unique reactivity allows researchers to design and synthesize new compounds with specific properties and functions, which can be further investigated for their potential applications in various industries.
Used in Material Science:
(alpha-ethoxyvinyl)triphenylphosphonium bromide's ability to participate in dehydrogenation, alkylation, and base hydrolysis reactions also makes it a promising candidate for the development of new materials with tailored properties. For instance, it can be used to synthesize novel polymers, catalysts, or other advanced materials that can find applications in areas such as electronics, energy storage, or environmental remediation.
Check Digit Verification of cas no
The CAS Registry Mumber 55552-25-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,5,5 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 55552-25:
(7*5)+(6*5)+(5*5)+(4*5)+(3*2)+(2*2)+(1*5)=125
125 % 10 = 5
So 55552-25-5 is a valid CAS Registry Number.
55552-25-5Relevant academic research and scientific papers
Ovakimyan,Barsegyan,Kikoyan,Indzhikyan
, p. 1069 - 1073 (2005)
Triphenyl- and tributyl[2-(2-phenylhydrazino)ethyl]phosphonium salts undergo dehydrogenation on heating to form the corresponding phenylhydrazones in high yields. The phenylhydrazone formed from the triphenylphosphonium salt can also be prepared from trip
