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2,5-dimethoxy-3,6-diphenylcyclohexa-2,5-diene-1,4-dione is a chemical compound with the molecular formula C18H16O4. It is a derivative of cyclohexadienedione, featuring two methoxy groups and two phenyl groups attached to the cyclohexadienedione ring. 2,5-dimethoxy-3,6-diphenylcyclohexa-2,5-diene-1,4-dione has garnered attention for its potential pharmaceutical applications, particularly as an anti-inflammatory and analgesic agent. Furthermore, it has been considered for use in organic synthesis and material science due to its unique structure and properties, making it a promising candidate for further research and development across various disciplines.

55458-24-7

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55458-24-7 Usage

Uses

Used in Pharmaceutical Applications:
2,5-dimethoxy-3,6-diphenylcyclohexa-2,5-diene-1,4-dione is used as an anti-inflammatory and analgesic agent for its potential to alleviate pain and reduce inflammation. Its chemical structure allows it to interact with biological targets, offering a new avenue for the treatment of conditions characterized by pain and swelling.
Used in Organic Synthesis:
In the field of organic synthesis, 2,5-dimethoxy-3,6-diphenylcyclohexa-2,5-diene-1,4-dione serves as a valuable intermediate or building block for the creation of more complex organic molecules. Its unique functional groups and structural features make it a versatile component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Material Science:
2,5-dimethoxy-3,6-diphenylcyclohexa-2,5-diene-1,4-dione is utilized in material science for its potential to contribute to the development of new materials with specific properties. Its incorporation into polymers or other materials could lead to advancements in areas such as electronics, coatings, or composite materials, where its structural attributes may impart enhanced performance characteristics.
Used in Research and Development:
2,5-dimethoxy-3,6-diphenylcyclohexa-2,5-diene-1,4-dione is employed in research and development settings to explore its chemical properties, reactivity, and potential applications in various industries. Scientists and researchers investigate its behavior under different conditions and interactions with other compounds to uncover new uses and optimize its performance in existing applications.

Check Digit Verification of cas no

The CAS Registry Mumber 55458-24-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,4,5 and 8 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 55458-24:
(7*5)+(6*5)+(5*4)+(4*5)+(3*8)+(2*2)+(1*4)=137
137 % 10 = 7
So 55458-24-7 is a valid CAS Registry Number.

55458-24-7Relevant academic research and scientific papers

Synthesis of a focused chemical library based on derivatives of embelin, a natural product with proapoptotic and anticancer properties

Viault, Guillaume,Gree, Danielle,Das, Saibal,Yadav, Jhillu Singh,Gree, Rene

, p. 1233 - 1241 (2011/04/17)

The synthesis of new derivatives of embelin, a natural inhibitor of X-linked inhibitor of apoptosis protein (XIAP) is described. The design of these new molecules involved introduction of aromatic groups directly linked to the benzoquinone core. To allow a large flexibility in the nature and the length of the added chain, the strategy involves first aSuzuki-Miyaura reaction with functionalized aromatics, yielding a first generation of molecules. Then, by appropriate use of the functional groups, a second generation of representative embelin derivatives was prepared.

An approach to 3,6-disubstituted 2,5-dioxybenzoquinones via two sequential Suzuki couplings. Three-step synthesis of leucomelone

Gan, Xianwen,Jiang, Wei,Wang, Wei,Hu, Lihong

supporting information; body text, p. 589 - 592 (2009/07/24)

(Chemical Equation Presented) Two sequential Suzuki coupling reactions have been developed for efficient synthesis of synthetically and biologically important 3,6-disubstituted 2,5-dioxybenzoquinone architectures in a highly chemoselective controlled mann

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