4413-26-7 Usage
Description
[1-(Hydroxyimino)ethyl]phenyl-diazene, with the molecular formula C8H9N3O, is an azo compound featuring a phenyl group connected to a nitrogen atom, to which a hydroxyiminoethyl group is also attached. [1-(Hydroxyimino)ethyl]phenyl-diazene is known for its stability and azo dye characteristics, making it a valuable asset in the realms of organic synthesis, chemical research, and the development of innovative materials and pharmaceuticals. Furthermore, it holds significant interest for studying chemical reactions and mechanisms involving azo compounds.
Uses
Used in Organic Synthesis:
[1-(Hydroxyimino)ethyl]phenyl-diazene is used as a key intermediate in the synthesis of various organic compounds. Its unique structure allows for a wide range of reactions, making it a versatile building block for creating complex molecules with potential applications in different industries.
Used in Chemical Research:
As a stable azo compound, [1-(Hydroxyimino)ethyl]phenyl-diazene is utilized in chemical research to study the properties and reactivity of azo compounds. This understanding can lead to the development of new synthetic methods and the discovery of novel chemical reactions.
Used in Material Development:
[1-(Hydroxyimino)ethyl]phenyl-diazene's azo dye properties make it a candidate for the development of new materials with specific characteristics, such as color, stability, or reactivity. These materials could find applications in various industries, including textiles, plastics, and coatings.
Used in Pharmaceutical Research:
[1-(Hydroxyimino)ethyl]phenyl-diazene's potential applications extend to the pharmaceutical industry, where it could be used as a starting material for the synthesis of new drugs or as a probe to study biological processes involving azo compounds.
Used in the Study of Chemical Reactions and Mechanisms:
[1-(Hydroxyimino)ethyl]phenyl-diazene's reactivity and structural features make it an interesting subject for researchers studying the mechanisms of chemical reactions involving azo compounds. This knowledge can contribute to the advancement of chemical science and the development of more efficient synthetic routes.
Check Digit Verification of cas no
The CAS Registry Mumber 4413-26-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,1 and 3 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4413-26:
(6*4)+(5*4)+(4*1)+(3*3)+(2*2)+(1*6)=67
67 % 10 = 7
So 4413-26-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H9N3O/c1-7(11-12)9-10-8-5-3-2-4-6-8/h2-6,12H,1H3
4413-26-7Relevant articles and documents
Polyaromatic hydrocarbon derivatized azo-oximes of cobalt(iii) for the ligand-redox controlled electrocatalytic oxygen reduction reaction
Dinda, Soumitra,Roy, Syamantak,Patra, Sarat Chandra,Bhandary, Subhrajyoti,Pramanik, Kausikisankar,Ganguly, Sanjib
, p. 3737 - 3747 (2020/03/17)
A pair of ligands HLPyr1a and HLAnc1b (Pyr = pyrene, Anc = anthracene) incorporating π-electron-rich polycyclic aromatic hydrocarbons (PAHs), viz. pyrene and anthracene moieties respectively, in conjunction with electron-poor azo-oxime groups was synthesized. The tris complexes [CoIII(LPyr)3] 2a and [CoIII(LAnc)3] 2b were also prepared and structurally authenticated by X-ray diffraction. They exhibit significant redox and optoelectronic properties, which were analyzed by density functional theory (DFT) and time dependent density functional theory (TD-DFT). Theoretical investigation further revealed that the coordinated ligands act as superior electron reservoirs in comparison to the free ligands and transfer electrons through the PAH moieties. This property was smartly exploited to scrutinize the aptitude of the cobalt(iii) complexes for the electrocatalytic oxygen reduction reaction (ORR). The catalytic process proceeds via a 4-electron transfer pathway to form hydroxide ions in alkaline medium. The role of the PAHs in the complexes 2a and 2b in providing a pool of electrons was further emphasized via substituting them with phenyl groups, as in [CoIII(LPh)3] 2c, when the catalytic ORR activity was significantly diminished. Moreover, the activity was completely lost when the PAHs were replaced by methyl groups, as in [CoIII(LMe)3] 2d.
