6343-76-6 Usage
Description
[(E)-cyano(phenylamino)methylidene]aminobenzene, a complex organic compound with the molecular formula C14H11N3, is derived from benzene and features a benzene ring with an amino group and a cyano group. A methylidene group is attached to the amino group, endowing the compound with multiple functional groups. This structural complexity suggests a wide range of potential applications in the chemical industry, as well as the possibility of diverse chemical properties that could be harnessed in various chemical reactions and processes. The unique structure also indicates potential for further modification and exploration in organic synthesis and pharmaceutical applications.
Uses
Used in Chemical Industry:
[(E)-cyano(phenylamino)methylidene]aminobenzene is used as a versatile compound for its multiple functional groups, which can be utilized in various chemical reactions and processes. The presence of the amino, cyano, and methylidene groups allows for a range of possible interactions and transformations, making it a valuable component in the synthesis of other complex molecules.
Used in Organic Synthesis:
In the field of organic synthesis, [(E)-cyano(phenylamino)methylidene]aminobenzene is used as a building block for the creation of more complex organic molecules. Its unique structure and functional groups provide opportunities for further modification and exploration, potentially leading to the development of novel compounds with specific properties and applications.
Used in Pharmaceutical Applications:
[(E)-cyano(phenylamino)methylidene]aminobenzene's diverse chemical properties and potential for modification make it a candidate for use in the pharmaceutical industry. It could be employed as a starting material or intermediate in the development of new drugs, particularly those targeting specific biological pathways or receptors.
Used in Research and Development:
[(E)-cyano(phenylamino)methylidene]aminobenzene is also used in research and development settings to study its chemical properties, reactivity, and potential applications. This can lead to a better understanding of its behavior in various chemical environments and the discovery of new uses in different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 6343-76-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,4 and 3 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6343-76:
(6*6)+(5*3)+(4*4)+(3*3)+(2*7)+(1*6)=96
96 % 10 = 6
So 6343-76-6 is a valid CAS Registry Number.
6343-76-6Relevant articles and documents
Chemistry of 4-chloro-5-cyano-1,2,3-dithiazolium chloride
Koutentis, Panayiotis A.,Rees, Charles W.
, p. 111 - 117 (2007/10/03)
The title compound 2, modelled on Appel salt 1, reacts as rapidly as 1 with phenols and anilines; since it lacks a good leaving group at the highly electrophilic C-5 position there is not one low energy reaction pathway, as there is with 1, and the reactions are complex giving more products in lower yields. With phenols it gives 2-aminobenzofuran-3-carbonitriles 3 resulting from initial nucleophilic attack through the phenolic ortho-carbon (Scheme 1). Aniline reacts with 2 largely through nitrogen to give 2-phenyliminopropanedinitrile 7 and the amidine 8, the bis-anilinomalononitrile 9 and the thioamide 10, all derived from 7 (Scheme 2). 1,4-Diaminobenzene reacts similarly with 2 to give the mono- and bis-dicyanoimines 22 and 23, whilst 1,2-diaminobenzene gives the cyclised product 2-aminoquinoxaline-3-carbonitrile 20. 1,8-Diaminonaphthalene gives the sulfur abstraction product, thiadiazine 24, and the quinomethane imine 25 and products derived from it (Scheme 7), in keeping with the high reactivity of the naphthalene ring towards electrophilic substitution. In all of these reactions with aromatic amines, salt 2 is acting as an equivalent of NC-C++-CN (umpolung of malononitrile) whilst with phenols it acts as an equivalent of dicyanocarbene, NC-C??-CN.
