6477-28-7 Usage
Ketone derivative
Structure This compound is a derivative of a ketone, which is a class of organic compounds with a carbonyl functional group (C=O) bonded to two carbon atoms.
Key intermediate
Synthesis This compound serves as a crucial intermediate in the synthesis of various important organic compounds, making it valuable in chemical research and production.
Applications
Pharmaceutical, agrochemical, and fragrance industries 1-phenyl-3-(2,4,6-trimethylphenyl)propane-1,3-dione is widely used in the production of pharmaceuticals, agrochemicals, and fragrances due to its versatile chemical properties.
Physical form
Yellowish to greenish crystalline powder The compound appears as a yellowish to greenish crystalline powder, which is a common form for many organic compounds.
Solubility
Insoluble in water, soluble in organic solvents 1-phenyl-3-(2,4,6-trimethylphenyl)propane-1,3-dione does not dissolve in water but can dissolve in many organic solvents, such as ethanol or acetone.
Hazardous nature
Potentially hazardous, strict safety protocols This compound is potentially hazardous, and it is essential to handle it with care and follow strict safety protocols to minimize risks to human health and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 6477-28-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,7 and 7 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6477-28:
(6*6)+(5*4)+(4*7)+(3*7)+(2*2)+(1*8)=117
117 % 10 = 7
So 6477-28-7 is a valid CAS Registry Number.
6477-28-7Relevant articles and documents
Synthesis of dibenzoylmethane derivatives and inhibition of mutagenicity in Salmonella typhimurium
Choshi,horimoto,Wang,Nagase,Ichikawa,Sugino,Hibino
, p. 1047 - 1049 (2007/10/02)
Twenty dibenzoylmethanes with methyl, methoxy, bromo, chloro, or fluoro substitution on either one or both benzene rings were synthesized and assayed for inhibition of the mutagenicity of 2-nitrofluorene in S. typhimurium TA98. 2,2-Dimethoxy, 3,3-dimethoxy and 3,3,4,4-tetramethoxydibenzoylmethane was as active as dibenzoylmethane. None of the halogen-substituted dibenzoylmethanes were active. These results demonstrate that dibenzoylmethanes can inhibit the mutagenicity of 2-nitrofluorene, and that modifications made on the benzene rings of dibenzoylmethane cannot enhance the antimutagenicity of this parent compound.
