474318-78-0 Usage
Uses
Used in Dye Industry:
[2,4-Dibromo-6-(methyl-NNO-azoxy)phenyl]amine is used as a dye intermediate for its ability to produce vibrant colors. It is particularly useful in the production of dyes for textiles and plastics, enhancing the visual appeal and colorfastness of these materials.
Used in Pigment Industry:
In addition to its role in the dye industry, [2,4-Dibromo-6-(methyl-NNO-azoxy)phenyl]amine is also utilized as a pigment in various industrial applications. Its color-enhancing properties make it a valuable component in the creation of pigments for a wide range of products, including inks, coatings, and paints.
Caution:
It is important to handle [2,4-Dibromo-6-(methyl-NNO-azoxy)phenyl]amine with care, as it may pose health risks if not properly managed. Safety measures should be taken to minimize exposure and ensure the well-being of those who work with this chemical compound.
Check Digit Verification of cas no
The CAS Registry Mumber 474318-78-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,4,3,1 and 8 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 474318-78:
(8*4)+(7*7)+(6*4)+(5*3)+(4*1)+(3*8)+(2*7)+(1*8)=170
170 % 10 = 0
So 474318-78-0 is a valid CAS Registry Number.
474318-78-0Relevant articles and documents
Selective reduction of the nitro group in the presence of the azoxy group. Synthesis of 2-(alkyl-NNO-azoxy)anilines
Lipilin, D. L.,Churakov, A. M.,Strelenko, Yu. A.,Tartakovsky, V. A.
, p. 311 - 318 (2007/10/03)
Tin(II) chloride selectively reduces the aromatic nitro group to the amino group, the azoxy group remaining intact. This allows the preparation of 2-(R-NNO-azoxy)anilines from 2-(R-NNO-azoxy)nitrobenzenes bearing electron-donating or weak electron-withdrawing substituents (Me or Br) in the benzene ring and alkyl substituents at the distal N atom of the azoxy group. The presence of electron-withdrawing substituents at the azoxy group (for example, CO2Et) leads to a change in the direction of the reaction resulting in selective reduction of the azoxy group to the hydrazo group.
