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[1,1':3',1''-Terphenyl]-2',5'-diol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13379-77-6

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13379-77-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13379-77-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,7 and 9 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 13379-77:
(7*1)+(6*3)+(5*3)+(4*7)+(3*9)+(2*7)+(1*7)=116
116 % 10 = 6
So 13379-77-6 is a valid CAS Registry Number.

13379-77-6Relevant academic research and scientific papers

Degradation of the adsorbent tenax TA by nitrogen oxides, ozone, hydrogen peroxide, OH radical, and limonene oxidation products

Kleno, Jacob G.,Wolkoff, Peder,Clausen, Per A.,Wilkins, Cornelius K.,Pedersen, Thorvald

, p. 4121 - 4126 (2002)

The degradation of the adsorbent Tenax TA was studied qualitatively by sampling oxidants common in indoor air followed by thermal desorption and gas chromatography. A total of 25 degradation products were identified. Several degradation products not reported previously were identified: 9 for nitrogen dioxide; 11 for ozone; 2 for hydrogen peroxide; 12 for hydroxyl radical; 1 for ozonelimonene mixtures, but none for nitrogen oxide. Whereas ozone shows a complex degradation of the adsorbent, hydrogen peroxide and limonene-ozone mixtures show few products. Nitrogen dioxide and the hydroxyl radical behave almost identically and produce 2,6-diphenyl-p-benzoquinone as the major degradation product. Reactant specific degradation products were identified for ozone (11) and nitrogen dioxide (1).

Synthesis of New Type Benzo[b]thiophene Fused Quinones and their Tetracyanoquinodimethane Derivatives

Ohba, Yoshihiro,Murakami, Yasuo,Sone, Tyo,Awano, Hiroshi

, p. 781 - 787 (2007/10/03)

A series of new type of benzo[b]thiophene-fused 1,4-benzoquinones and their tetracyanoquinodimethane derivatives were synthesized. The cyclic voltammetric data of new type quinones and tetracyanoquinodimethane derivatives displayed different behavior. All new quinones exhibit two reduction waves corresponding to the radical anion and dianion. On the other hand, most tetracyanoquinodunethane derivatives display a singlewave reduction to the dianion. The benzo[b]thiophene moiety fused tetracyanoquinodimethane derivatives reveal more negative reduction potentials than that of tetracyanoquinodimethane.

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