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4,5-dibromocyclohexa-3,5-diene-1,2-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55759-50-7

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55759-50-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55759-50-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,7,5 and 9 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 55759-50:
(7*5)+(6*5)+(5*7)+(4*5)+(3*9)+(2*5)+(1*0)=157
157 % 10 = 7
So 55759-50-7 is a valid CAS Registry Number.

55759-50-7Relevant academic research and scientific papers

Bromination Improves the Electron Mobility of Tetraazapentacene

Reiss, Hilmar,Ji, Lei,Han, Jie,Koser, Silke,Tverskoy, Olena,Freudenberg, Jan,Hinkel, Felix,Moos, Michael,Friedrich, Alexandra,Krummenacher, Ivo,Lambert, Christoph,Braunschweig, Holger,Dreuw, Andreas,Marder, Todd B.,Bunz, Uwe H. F.

, p. 9543 - 9547 (2018)

A cyclocondensation of TIPS-ethynyl-substituted diaminoarenes with in situ obtained 4,5-dibromocyclohexa-3,5-diene-1,2-dione has led to the synthesis of tetrabromotetraazapentacene (BrTAP). BrTAP is easily reduced to its air-stable radical anion and elect

Cyclodimers and Cyclotrimers of 2,3 -Bisalkynylated Anthracenes, Phenazines and Diazatetracenes

Bunz, Uwe H. F.,Freudenberg, Jan,Hippchen, Nikolai,Maier, Steffen,Rominger, Frank

supporting information, p. 16320 - 16324 (2021/11/10)

The synthesis of novel (N?)acene-based cyclooligomers is reported. Glaser-Hay coupling of the bisethynylated monomers results in cyclodimers and cyclotrimers that are separable by column and gel-permeation chromatographies. For the diazatetracene, the use

Synthesis of Mercapturic Acid Derivatives of Putative Toxic Metabolites of Bromobenzene

Hanzlik, Robert P.,Weller, Paul E.,Desai, Jayant,Zheng, Jiang,Hall, Larry R.,Slaughter, Donald E.

, p. 2736 - 2742 (2007/10/02)

The synthesis and characterization of nine isomerically defined S-arylmercapturic acids of interest in connection with the metabolism of the model hepatotoxin bromobenzene is described.Included are three S-(bromophenyl)-, two S-(bromohydroxyphenyl)-, and three S-(bromodihydroxyphenyl)mercapturic acids of defined substitution pattern.In addition, several related compounds with two or no bromine atoms are described.These syntheses depend on two basic methods, 1,4-addition of various arene thiols to acetamidoacrylic acid or the 1,4-addition of N-acetyl-L-cysteine to various benzoquinone derivatives.In addition, we describe a method for efficient conversion of the mercapturic acids to thioanisole derivatives, regioisomers of which can be separed and detected at low levels by capillary gas-liquid chromatography.

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