75304-65-3 Usage
Description
4-[(E)-(2-chlorophenyl)diazenyl]-3,5-dimethyl-1H-pyrazol-1-yl(pyridin-4-yl)methanone is a complex chemical compound belonging to the class of pyrazole derivatives. It features a diazenyl group and a pyridinyl group, contributing to its unique chemical properties. With a molecular formula of C18H16ClN7O and a molecular weight of 375.5 g/mol, this compound is known for its application as a reagent in chemical reactions and as a building block in organic synthesis. Although its potential pharmacological properties are of interest, further research is necessary to explore its full range of possible uses and effects.
Uses
Used in Chemical Synthesis:
4-[(E)-(2-chlorophenyl)diazenyl]-3,5-dimethyl-1H-pyrazol-1-yl(pyridin-4-yl)methanone is used as a reagent in the chemical synthesis industry for its ability to participate in various chemical reactions. Its unique structure allows it to be a valuable building block in creating more complex molecules.
Used in Organic Synthesis:
In the field of organic synthesis, 4-[(E)-(2-chlorophenyl)diazenyl]-3,5-dimethyl-1H-pyrazol-1-yl(pyridin-4-yl)methanone serves as a key component in the development of novel organic compounds. Its versatility in reacting with other molecules makes it a promising candidate for creating new substances with potential applications in various industries.
Used in Pharmaceutical Research:
The potential pharmacological properties of 4-[(E)-(2-chlorophenyl)diazenyl]-3,5-dimethyl-1H-pyrazol-1-yl(pyridin-4-yl)methanone make it a candidate for further research in the pharmaceutical industry. Its unique structure may lead to the discovery of new drugs or therapeutic agents, pending further investigation into its biological activities and safety profile.
Used in Material Science:
4-[(E)-(2-chlorophenyl)diazenyl]-3,5-dimethyl-1H-pyrazol-1-yl(pyridin-4-yl)methanone's complex structure and chemical properties may also find applications in material science, where it could be utilized in the development of new materials with specific properties, such as improved conductivity, stability, or reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 75304-65-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,3,0 and 4 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 75304-65:
(7*7)+(6*5)+(5*3)+(4*0)+(3*4)+(2*6)+(1*5)=123
123 % 10 = 3
So 75304-65-3 is a valid CAS Registry Number.