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2,5-Cyclohexadiene-1,4-dione, 2-chloro-6-(2,4,6-trichlorophenoxy)- is a complex organic chemical compound with the molecular formula C12H5Cl5O3. It is a derivative of cyclohexadiene-dione, featuring a chlorinated phenoxy group attached to the cyclohexadiene ring. 2,5-Cyclohexadiene-1,4-dione, 2-chloro-6-(2,4,6-trichlorophenoxy)- is characterized by its unique structure, which includes a cyclohexadiene ring with two carbonyl groups at the 1 and 4 positions, a chlorine atom at the 2 position, and a 2,4,6-trichlorophenoxy group at the 6 position. The compound may have potential applications in various chemical industries, such as the synthesis of pharmaceuticals, agrochemicals, or other specialty chemicals, due to its reactive functional groups and unique structure. However, it is important to note that the specific uses and properties of 2,5-Cyclohexadiene-1,4-dione, 2-chloro-6-(2,4,6-trichlorophenoxy)- would require further investigation and characterization.

7714-21-8

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7714-21-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7714-21-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,1 and 4 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7714-21:
(6*7)+(5*7)+(4*1)+(3*4)+(2*2)+(1*1)=98
98 % 10 = 8
So 7714-21-8 is a valid CAS Registry Number.

7714-21-8Relevant academic research and scientific papers

Formation of dimer-type ketals in the reaction of 2,4,6-trichlorophenol and 2,4,6-trichloro-m-cresol with calcium hypochlorite in methanol: Conversion to quinones and other compounds

Heasley, Victor L.,Anderson, James D.,Bowman, Zachery S.,Hanley Jr., John C.,Sigmund, Geoffery A.,Van Horn, David,Shellhamer, Dale F.

, p. 6827 - 6830 (2007/10/03)

2,4,6-Trichlorophenol (2) and 2,4,6-trichloro-m-cresol (5) react with calcium hypochlorite (Ca(OCl)2) in MeOH to give respectively dimer-type ketals 2-(2′,4′,6′-trichlorophenoxy)-4,4-dimethoxy-6 -chlorocyclohexadien-2,5-one (6) and 2-(3′-methyl-2′,4′,6′-trichlorophenoxy)-4, 4-di-methoxy-5-methyl-6-chlorocyclohexadien-2,5-one (7). Ketal 6, which was too unstable to be isolated, and 7 hydrolyzed in H2O/HCl to 2-(2′,4′,6′-trichlorophenoxy)-6-chloro-1,4-ben-zoquinone (8) and 2-(3′-methyl-2′,4′,6′-trichlorophenoxy)-5 -methyl-6-chloro-1,4-benzoquinone (9), respectively. Ketal 6 and quinone 8 were also produced when 2 and Ca(OCl)2 reacted in DMF, followed by addition of MeOH and H2O, respectively. The mechanisms of these reactions are examined. Conversion of the ketals and quinones to other products is described.

Barium manganate oxidation in organic synthesis: Part - V: Oxidation of phenols

Srivastava,Venkataramani

, p. 35 - 45 (2007/10/02)

Oxidation of phenols, specially the hindered phenols has been carried out with barium manganate in non-aqueous media under heterogeneous conditions and the results of these studies are described in this paper.

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