51764-05-7 Usage
Uses
Used in Organic Synthesis:
2,3-diphenylpentanedinitrile is utilized as a precursor in the synthesis of various organic compounds, providing a foundation for the creation of complex molecules. Its presence in the synthesis process is crucial for the development of new chemical entities with potential applications in different fields.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 2,3-diphenylpentanedinitrile is employed as a building block for the production of complex molecules. Its structural properties make it a valuable component in the design and synthesis of new pharmaceutical agents, contributing to the development of innovative treatments and therapies.
Used in Agrochemical Industry:
2,3-diphenylpentanedinitrile also finds application in the agrochemical industry, where it is used in the synthesis of compounds with potential pesticidal or herbicidal properties. Its role in this industry is pivotal for the development of new agrochemicals aimed at enhancing crop protection and productivity.
Used in Research and Development:
2,3-diphenylpentanedinitrile is also used in research and development settings to explore its biological activity and pharmacological properties. Studies on 2,3-diphenylpentanedinitrile are conducted to understand its potential as a therapeutic agent and to uncover new avenues for its application in medicine and other industries.
Check Digit Verification of cas no
The CAS Registry Mumber 51764-05-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,7,6 and 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 51764-05:
(7*5)+(6*1)+(5*7)+(4*6)+(3*4)+(2*0)+(1*5)=117
117 % 10 = 7
So 51764-05-7 is a valid CAS Registry Number.
51764-05-7Relevant academic research and scientific papers
Reconstructed hydrotalcite as a highly active heterogeneous base catalyst for carbon-carbon bond formations in the presence of water
Ebitani, Kohki,Motokura, Ken,Mori, Kohsuke,Mizugaki, Tomoo,Kaneda, Kiyotomi
, p. 5440 - 5447 (2007/10/03)
The aldol reaction of carbonyl compounds is efficiently catalyzed by reconstructed hydrotalcites, obtained by treating the Mg-Al mixed oxide with water, as solid base catalysts in the presence of water. The catalysis of the reconstructed hydrotalcites is attributable to the surface base sites, created during the organization of the layered structure, with uniformly distributed strength. Furthermore, the reconstructed hydrotalcites provide a unique acid-base bifunctional surface capable of promoting the Knoevenagel and Michael reactions of nitriles with carbonyl compounds.
Water-soluble calixarenes as new inverse phase-transfer catalysts. Their application to aldol-type condensation and Michael addition reactions in water
Shimizu, Shoichi,Shirakawa, Seiji,Suzuki, Takashi,Sasaki, Yasuyuki
, p. 6169 - 6173 (2007/10/03)
Aldol-type condensation and Michael addition reactions of activated methyl and methylene compounds in aqueous NaOH solution have been developed without the need for any added organic solvents. The water-soluble calix[n]arenes, which contain trimethylammon
EXTENSION DE LA REACTION DE MICHAEL EN PRESENCE CsF/Si(OR)4
Boyer, J.,Corriu, R. J. P.,Perz, R.,Reye, C.
, p. 117 - 122 (2007/10/02)
An extension of the Michael reaction is described.CsF in the presence of Si(OR)4 is found to be very efficient for carrying out Michael additions of monoketones and arylacetonitriles on different kinds of Michael acceptors: α,β unsaturated ketones, esters
