30866-56-9 Usage
Uses
Used in Organic Synthesis:
1-(2-chlorophenyl)-5-phenylpentane-1,3,5-trione is used as an intermediate in the synthesis of various organic compounds. Its unique structure allows for a range of chemical transformations, making it a valuable building block for the creation of new molecules with specific properties and functions.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 1-(2-chlorophenyl)-5-phenylpentane-1,3,5-trione is used as a starting material for the development of novel drugs. Its potential reactivity and structural diversity enable researchers to explore its applications in the design and synthesis of new therapeutic agents.
Used in Chemical Reactions:
Due to its complex structure, 1-(2-chlorophenyl)-5-phenylpentane-1,3,5-trione is used as a reactant in various chemical reactions. Its aromatic and aliphatic characteristics facilitate interactions with other molecules, making it a useful compound for studying reaction mechanisms and developing new synthetic methods.
Check Digit Verification of cas no
The CAS Registry Mumber 30866-56-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,8,6 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 30866-56:
(7*3)+(6*0)+(5*8)+(4*6)+(3*6)+(2*5)+(1*6)=119
119 % 10 = 9
So 30866-56-9 is a valid CAS Registry Number.
30866-56-9Relevant academic research and scientific papers
Thermal addition reaction of aroylketene with 1-aryl-1- trimethylsilyloxyethylenes: Aromatic substituent effects of aroylketene and aryltrimethylsilyloxyethylene on their reactivity
Saitoh,Oyama,Sakurai,Niimura,Hinata,Horiguchi,Toda,Sano
, p. 956 - 966 (2007/10/03)
The thermal addition reaction of various aroylketenes (C) generated by the thermolysis of 5-aryldioxofurans (A) to 1-aryl-1-trimethylsilyloxyethylenes gave 1,5-diarylpentane-1,3,5-triones (D) and 2,6-diaryl-4H-pyran-4-ones (E). The introduction of electron withdrawing substituents in the aroylketene and of electron donating substituents facilitated the addition reaction. The observed substituent effects and the reaction mechanism are interpreted in terms of molecular orbital analyses.
