6342-95-6 Usage
Uses
Used in Organic Synthesis:
(4-nitrophenyl)(2,3,4-trimethoxyphenyl)methanone is used as an intermediate in the synthesis of various organic compounds. Its unique structure allows for further functionalization and modification, making it a valuable building block for creating complex organic molecules.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (4-nitrophenyl)(2,3,4-trimethoxyphenyl)methanone is used as a starting material for the development of new drugs. Its potential biological activities and chemical properties make it a promising candidate for the creation of novel therapeutic agents.
Used in Chemical Research:
(4-nitrophenyl)(2,3,4-trimethoxyphenyl)methanone is also utilized in chemical research to study the properties and reactivity of phenylpropanoids and polyketides. This helps in understanding the structure-activity relationships and the potential applications of these compounds in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 6342-95-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,4 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6342-95:
(6*6)+(5*3)+(4*4)+(3*2)+(2*9)+(1*5)=96
96 % 10 = 6
So 6342-95-6 is a valid CAS Registry Number.
6342-95-6Relevant academic research and scientific papers
On the synthesis and biological properties of isocombretastatins: A case of ketone homologation during Wittig reaction attempts
Stocker, Vivien,Ghinet, Alina,Leman, Marie,Rigo, Benoit,Millet, Regis,Farce, Amaury,Desravines, Deborah,Dubois, Joelle,Waterlot, Christophe,Gautret, Philippe
, p. 3683 - 3696 (2013/04/11)
New isocombretastatins were synthesized by reacting the corresponding phenstatin analogs with CH3PPh3Br in presence of tBuOK. These new derivatives showed significant activities against cellular proliferation and tubulin polymerization. In particular, monomethoxylated derivatives of phenstatin and isoCA-4 exhibit similar activities to those of parent phenstatin. Attempts of the Wittig reaction on 2- (or 4-) methoxy-4′-nitrobenzophenones in the same conditions do not lead to the expected isocombretastatins but to methyleneketones with the exclusion of triphenylphosphine. A mechanism for this new ketone homologation was proposed.
