6565-32-8 Usage
Physical state
Colorless liquid The compound appears as a colorless liquid, which means it does not have a color and is in a liquid state at room temperature.
Solubility
Insoluble in water, soluble in organic solvents This property indicates that the compound does not dissolve well in water but dissolves easily in organic solvents, such as alcohols, ethers, and hydrocarbons.
Uses
Building block in pharmaceuticals and agrochemicals, intermediate in fragrances and flavorings The compound is commonly used as a starting material in the synthesis of pharmaceuticals and agrochemicals, as well as an intermediate in the production of fragrances and flavorings.
Biological activity
Enhances the biological activity of organic molecules The presence of this compound in a molecule can improve its ability to interact with biological systems, making it more effective in its intended application.
Safety precautions
Causes skin and eye irritation, hazardous if ingested or inhaled It is important to handle this chemical with care, as it can cause irritation to the skin and eyes, and can be harmful if swallowed or breathed in.
Check Digit Verification of cas no
The CAS Registry Mumber 6565-32-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,6 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6565-32:
(6*6)+(5*5)+(4*6)+(3*5)+(2*3)+(1*2)=108
108 % 10 = 8
So 6565-32-8 is a valid CAS Registry Number.
6565-32-8Relevant articles and documents
Ni-NiO heterojunctions: a versatile nanocatalyst for regioselective halogenation and oxidative esterification of aromatics
Bhardwaj, Nivedita,Goel, Bharat,Indra, Arindam,Jain, Shreyans K.,Singh, Ajit Kumar,Tripathi, Nancy
, p. 14177 - 14183 (2021/08/16)
Herein, we report a facile method for the synthesis of Ni-NiO heterojunction nanoparticles, which we utilized for the nuclear halogenation reaction of phenol and substituted phenols usingN-bromosuccinimide (NBS). A remarkablepara-selectivity was achieved for the halogenated products under semi-aqueous conditions. Interestingly, blocking of thepara-position of phenol offeredortho-selective halogenation. In addition, the Ni-NiO nanoparticles catalyzed the oxidative esterification of carbonyl compounds with alcohol, diol or dithiol in the presence of a catalytic amount of NBS. It was observed that the aromatic carbonyls substituted with an electron-donating group favoured nuclear halogenation, whereas an electron-withdrawing group substitution in carbonyl compounds facilitated the oxidation reaction. In addition, the catalyst was magnetically separated and recycled 10 times. The tuned electronic structure at the Ni-NiO heterojunction controlled selectivity and activity as no suchpara-selectivity was observed with commercially available NiO or Ni nanoparticles.
