13565-45-2 Usage
Uses
Used in Pharmaceutical and Agrochemical Synthesis:
(E)-3-(4-chlorophenyl)-1-o-tolylprop-2-en-1-one is used as a starting material for the synthesis of various pharmaceuticals and agrochemicals. Its unique chemical structure allows for the creation of a wide range of compounds with potential therapeutic and pesticidal properties.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (E)-3-(4-chlorophenyl)-1-o-tolylprop-2-en-1-one is used as a valuable compound for further study. Its demonstrated biological activities and pharmacological properties make it a promising candidate for the development of new drugs and therapeutic agents.
Used in Organic Chemistry:
(E)-3-(4-chlorophenyl)-1-o-tolylprop-2-en-1-one is also utilized in organic chemistry for the synthesis of other organic compounds. Its versatility in chemical reactions and its unique structure contribute to its importance in this field.
Used in Laboratory Settings:
(E)-3-(4-chlorophenyl)-1-o-tolylprop-2-en-1-one is commonly used in research and laboratory settings for various experiments and studies. Its properties make it a useful tool for understanding the behavior of similar compounds and for developing new synthetic methods.
Check Digit Verification of cas no
The CAS Registry Mumber 13565-45-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,5,6 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 13565-45:
(7*1)+(6*3)+(5*5)+(4*6)+(3*5)+(2*4)+(1*5)=102
102 % 10 = 2
So 13565-45-2 is a valid CAS Registry Number.
13565-45-2Relevant academic research and scientific papers
Zhang, Ning,Yang, Daoshan,Wei, Wei,Yuan, Li,Nie, Fafa,Tian, Laijin,Wang, Hua
, p. 3258 - 3263 (2015)
A silver-catalyzed double-decarboxylative protocol has been proposed for the construction of chalcone derivatives via cascade coupling of substituted α-keto acids with cinnamic acids under the mild aqueous conditions. The developed method for constructing C-C bonds via double-decarboxylative reactions is efficient, practical, and environmentally benign by using the readily available starting materials. It should provide a promising synthesis candidate for the formation of diverse and useful chalcone derivatives in the fields of synthetic and pharmaceutical chemistry.
