1572-57-2 Usage
Uses
Used in Organic Synthesis:
[(1E)-2,2,2-trichloroethanimidoyl]propanedinitrile is utilized as a reagent in organic synthesis, specifically for the preparation of a range of nitrogen-containing compounds. Its unique structure allows for the creation of diverse chemical products with potential applications in different industries.
Used in Pesticide and Herbicide Development:
[(1E)-2,2,2-trichloroethanimidoyl]propanedinitrile has been investigated for its potential pesticidal and herbicidal properties, making it a candidate for the development of new and effective solutions in agriculture to control pests and weeds.
Used in Pharmaceutical Industry:
[(1E)-2,2,2-trichloroethanimidoyl]propanedinitrile may also find applications in the pharmaceutical industry, where it could be used in the development of new drugs. Its reactivity and unique chemical structure could be harnessed to create novel therapeutic agents.
Used in Research and Development:
Due to its highly reactive and toxic nature, [(1E)-2,2,2-trichloroethanimidoyl]propanedinitrile is primarily used in controlled laboratory settings for research and development purposes. Scientists can explore its properties and potential applications in a safe and controlled environment.
Check Digit Verification of cas no
The CAS Registry Mumber 1572-57-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,7 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1572-57:
(6*1)+(5*5)+(4*7)+(3*2)+(2*5)+(1*7)=82
82 % 10 = 2
So 1572-57-2 is a valid CAS Registry Number.
1572-57-2Relevant academic research and scientific papers
Copper-catalyzed N-arylation of the adduct of malononitrile and trichloroacetonitrile
Nematpour, Manijeh,Abedi, Elham,Abedi, Elahe,Lotfi, Mahbob
, p. 727 - 730 (2018/09/26)
The synthesis of a novel class of trichloro-1-{(N-arylamino)ethylidene}malononitrile via a copper-catalyzed multicomponent reaction of malononitrile-trichloroacetonitrile adduct and aryl hal-ides in good yields is described. The reported protocol has some advantages such as simple and mild procedure, easy work-up, no column chromatography, available starting materials-catalyst, pure products and good to high yields.
NEW ONE-POT SYNTHESIS OF ENAMINEDINITRILES
Berry, Robert W. H.,Drewry, Peter C.,Hodson, Harold F.
, p. 958 - 975 (2007/10/02)
A convenient procedure is reported for the one-pot preparation of enaminedinitriles.This involves the sodium methoxide-catalysed addition of methanol to a suitably substituted nitrile followed by reaction of the resulting imidate with malononitrile.The mechanism, scope and limitations of the synthesis have been investigated.Spectroscopic evidence is presented that the products exist in the enaminedinitrile rather than in the tautomeric imino form.Various reactions of the compounds including halogen exchange, anion formation and amine displacement have been studied and used to extend the range of enaminedinitriles prepared.
