5778-00-7 Usage
Uses
Used in Pharmaceutical Research:
(2-Benzoylphenyl)(4-chlorophenyl)methanone is utilized as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of drugs with specific therapeutic properties, making it a valuable component in medicinal chemistry.
Used in Organic Synthesis:
As a ketone derivative, (2-benzoylphenyl)(4-chlorophenyl)methanone serves as a versatile building block in organic synthesis. It can be used to create a wide range of organic compounds, contributing to the advancement of chemical research and the creation of novel molecules with potential applications.
Used in Materials Science:
(2-Benzoylphenyl)(4-chlorophenyl)methanone may possess properties that make it useful in the synthesis of materials with specific characteristics. Its incorporation into materials science research can lead to the development of new materials with tailored properties for various applications.
Used in Nanotechnology:
(2-benzoylphenyl)(4-chlorophenyl)methanone's unique structure and properties also make it a candidate for use in nanotechnology. It can potentially be employed in the design and synthesis of nanoscale materials and devices, contributing to the advancement of this cutting-edge field.
Check Digit Verification of cas no
The CAS Registry Mumber 5778-00-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,7 and 8 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5778-00:
(6*5)+(5*7)+(4*7)+(3*8)+(2*0)+(1*0)=117
117 % 10 = 7
So 5778-00-7 is a valid CAS Registry Number.
5778-00-7Relevant academic research and scientific papers
Copper-catalyzed benzylic C-H oxygenation under an oxygen atmosphere via N-H imines as an intramolecular directing group
Zhang, Line,Ang, Gim Yean,Chiba, Shunsuke
, p. 1622 - 1625 (2011/05/05)
Copper-catalyzed benzylic C-H oxygenation under an oxygen atmosphere was developed starting from carbonitriles and Grignard reagents via N-H imine intermediates. The present process is characterized by the following two-step sequence in a one-pot manner: (1) addition of Grignard reagents to carbonitriles to form N-H imines and (2) benzylic C-H oxygenation (C=O bond formation) triggered by 1,5-hydrogen atom transfer with transient iminyl copper species.
