7149-37-3 Usage
Uses
Used in Organic Synthesis:
4-Benzoyl-1,3,5,7-tetraphenylheptane-1,7-dione is utilized as a reactant in organic synthesis, where its unique structure allows for the formation of a wide range of new compounds through various chemical reactions. Its ketone functional group and phenyl rings provide multiple sites for further functionalization, making it a versatile component in the synthesis of complex organic molecules.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 4-benzoyl-1,3,5,7-tetraphenylheptane-1,7-dione is employed as a building block for the creation of novel drug candidates. Its structural features may contribute to the development of new therapeutic agents with unique pharmacological properties, potentially leading to advancements in the treatment of various diseases and medical conditions.
Used in Material Science:
4-Benzoyl-1,3,5,7-tetraphenylheptane-1,7-dione also finds application in material science, where it can be incorporated into the design and synthesis of new materials with specific properties. Its chemical structure may be leveraged to create materials with tailored characteristics for use in various applications, such as in electronics, coatings, or other high-tech industries.
Check Digit Verification of cas no
The CAS Registry Mumber 7149-37-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,4 and 9 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7149-37:
(6*7)+(5*1)+(4*4)+(3*9)+(2*3)+(1*7)=103
103 % 10 = 3
So 7149-37-3 is a valid CAS Registry Number.
7149-37-3Relevant academic research and scientific papers
First authentication of Kostanecki's triketone and multimolecular reaction of aromatic aldehydes with acetophenone
Shan, Zixing,Hu, Xiaoyun,Hu, Lin,Peng, Xitian
experimental part, p. 1102 - 1111 (2009/10/17)
A double-component, multimolecular reaction between acetophenone and aromatic aldehydes was achieved under catalysis by the solid-base mixture NaOH/K2CO3, and Kostanecki's triketone, supposed to exist for more than 110 years, was suc
