153358-05-5 Usage
Uses
Used in Chemical Synthesis:
2-(Diphenylphosphino)benzaldehyde oxime, 95% is used as a reagent for the synthesis of various organic compounds. Its unique structure allows it to participate in a range of chemical reactions, making it a valuable tool in the synthesis of complex molecules.
Used in Catalysis:
2-(Diphenylphosphino)benzaldehyde oxime, 95% is used as a catalyst in the rearrangement and dehydration of aldoximes. Its phosphino group and oxime functionality enable it to facilitate these reactions, leading to the formation of desired products with improved efficiency and selectivity.
Used in Pharmaceutical Industry:
2-(Diphenylphosphino)benzaldehyde oxime, 95% is used as a catalyst in the synthesis of pharmaceutical compounds. Its ability to promote the rearrangement and dehydration of aldoximes can be particularly useful in the production of complex drug molecules, potentially leading to more efficient and cost-effective manufacturing processes.
Used in Research and Development:
2-(Diphenylphosphino)benzaldehyde oxime, 95% is used as a research tool in the development of new synthetic methods and catalytic processes. Its unique properties make it an interesting candidate for exploring novel reaction pathways and improving existing synthetic strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 153358-05-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,3,5 and 8 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 153358-05:
(8*1)+(7*5)+(6*3)+(5*3)+(4*5)+(3*8)+(2*0)+(1*5)=125
125 % 10 = 5
So 153358-05-5 is a valid CAS Registry Number.
153358-05-5Relevant academic research and scientific papers
Mild and efficient copper-catalyzed N-arylation of alkylamines and N-H heterocycles using an oxime-phosphine oxide ligand
Xu, Lei,Zhu, Di,Wu, Fan,Wang, Rongliang,Wan, Boshun
, p. 6553 - 6560 (2007/10/03)
A mild and efficient copper-catalyzed system for N-arylation of alkylamines and N-H heterocycles with aryl iodides using a novel, readily prepared and highly stable oxime-functionalized phosphine oxide ligand was developed. The coupling reactions could even be performed in solvent-free conditions with moderate to good yields.
POLYMERIZABLE DERIVATIVES OF TRIPHENYLPHOSPHINE. ACYLATION OF TRIARYLPHOSPHINES BEARING ALCOHOL OR AMINE SUBSTITUENTS WITH ACRYLOYLCHLORIDE AND METHACRYLOYLCHLORIDE
Nikitidis, Antonios,Andersson, Carlaxel
, p. 141 - 152 (2007/10/02)
Methods to prepare amino substituted triaryl-phosphines viz.N-methyl-2-(diphenylphosphino)benzylamine, N-t-butyl-2-(diphenylphosphino)benzylamine and α,N-dimethyl-4-(diphenylphosphino)benzylamine are presented.The acylation of amino and alcohol substituted triarylphosphines have been studied and the amides N-methacryloyl-N-methyl-4-(diphenylphosphino)benzylamine, N-methacryloyl-2-(diphenylphosphino)aniline, N-methacryloyl-N-methyl-4-(diphenylphosphino)benzylamine, N-methyl-N-propionyl-4-(diphenylphosphino)benzylamine, N-methyl-N-propionyl-2-(diphenylphosphino)benzylamine and N-acryloyl-N-methyl-4-(diphenylphosphino)benzylamine and the ester 2-(diphenylphosphino)benzyl methacrylate have been prepared. Key words: Phosphine; monomer; acylation; acryloylchloride; methacryloylchloride polymer-bound.
