1222-47-5 Usage
Uses
Used in Specialty Plastics and Polymers Industry:
Pentanedinitrile, 2,4-diphenylis used as a key intermediate in the production of specialty plastics and polymers. Its unique chemical structure and properties make it suitable for creating high-performance materials with specific characteristics required in various applications.
Used in Chemical Synthesis:
As a reactive compound, Pentanedinitrile, 2,4-diphenylis utilized in chemical synthesis processes to produce a variety of other compounds with different functionalities. Its versatility in reactions allows for the creation of new molecules with potential applications in various industries.
Used in Research and Development:
Due to its unique properties and reactivity, Pentanedinitrile, 2,4-diphenylis often used in research and development settings to explore new chemical reactions, synthesis pathways, and potential applications. Its use in research helps advance the understanding of chemical behavior and contributes to the development of new materials and technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 1222-47-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,2 and 2 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1222-47:
(6*1)+(5*2)+(4*2)+(3*2)+(2*4)+(1*7)=45
45 % 10 = 5
So 1222-47-5 is a valid CAS Registry Number.
1222-47-5Relevant academic research and scientific papers
A New Syntethic Route to Vinyl Sulfides Utilizing the Reaction of (Phenylthio)carbenes with Nitrile Anions
Harada, Toshiro,Karasawa, Akio,Oku, Akira
, p. 842 - 846 (2007/10/02)
Reactions of nitrile anion (LiCR2R3CN) and (phenylthio)carbenes generated from 1-chloroalkyl phenyl sulfides (R1CH(Cl)SPh) 2a-e by the action of n-BuLi have been shown to be a useful synthetic route to vinyl sulfides (PhSC(R1)=CR2R3) 3a-k (34-91percent).The nucleophilic attack of the nitrile anion on the carbenic species gave the presumed intermediate β-(phenylthio)-β-lithionitrile, which eliminated LiCN to give the expected vinyl sulfides.The application of the present reaction to the synthesis of cyclic vinyl sulfides was successful: the decomposition of the dianion ofω,ω-bis(phenylthio)alkanenitriles (8b, 8c, 11, and 14) affording the corresponding 1-(phenylthio)cycloalkenes (9, 10, 12, and 15) in 12-87percent yields.
