27761-33-7 Usage
Uses
Used in Organic Synthesis:
4-[(2,5-dimethylphenyl)hydrazono]cyclohexa-2,5-dien-1-one is used as a synthetic intermediate for the preparation of various organic compounds due to its reactivity and the ability to form new compounds with diverse applications.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 4-[(2,5-dimethylphenyl)hydrazono]cyclohexa-2,5-dien-1-one is used as a potential lead compound for the development of new drugs. Its unique structure and reactivity may contribute to the discovery of novel therapeutic agents.
Used in Biological Activity Studies:
4-[(2,5-dimethylphenyl)hydrazono]cyclohexa-2,5-dien-1-one is used as a subject of biological activity studies to explore its potential uses in medicine. Further research is needed to understand its interactions with biological systems and its therapeutic potential.
Due to the presence of the hydrazone group, 4-[(2,5-dimethylphenyl)hydrazono]cyclohexa-2,5-dien-1-one may exhibit interesting chemical properties, such as the ability to react with various functional groups, which could lead to the formation of new compounds with a wide range of applications across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 27761-33-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,7,6 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 27761-33:
(7*2)+(6*7)+(5*7)+(4*6)+(3*1)+(2*3)+(1*3)=127
127 % 10 = 7
So 27761-33-7 is a valid CAS Registry Number.
27761-33-7Relevant academic research and scientific papers
Modified clays as efficient acid-base catalyst systems for diazotization and diazocoupling reactions
Bahulayan, Damodaran,John, Litka,Lalithambika, Malathy
, p. 863 - 869 (2007/10/03)
Diazotization and diazocoupling reactions of aniline and its substituted derivatives with phenol and other aromatic amines over ecofriendly clay catalysts is described. This inexpensive, non-corrosive and reusable catalysts were found to exhibit bifunctional catalytic properties for these reactions. No considerable decrease in the efficiency of the catalysts were observed after five cycles of operation. The new method totally avoids the use of acids and alkalies.
