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1,2-Bis(4-p-toluenesulfonyl-1,4,7-triazacyclonon-1-yl)ethane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1056967-99-7

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1056967-99-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1056967-99-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,6,9,6 and 7 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1056967-99:
(9*1)+(8*0)+(7*5)+(6*6)+(5*9)+(4*6)+(3*7)+(2*9)+(1*9)=197
197 % 10 = 7
So 1056967-99-7 is a valid CAS Registry Number.

1056967-99-7Downstream Products

1056967-99-7Relevant academic research and scientific papers

Neuroprotection and cardioprotection afforded by chelators with high affinity and specificity for cations of first transition series elements

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, (2008/06/13)

Compounds that demonstrate chelation affinity and selectivity for first transition series elements are administered to patients suffering from such conditions as ischemia, prolonged seizures and trauma to provide neuroprotection, cardioprotection, or both. These compounds when administered form complexes with chelatable iron and copper cations and thereby mitigate the ability of these cations to catalyze Haber-Weiss reactions that form toxic hydroxy free radicals that cause tissue injury. These compounds also form complexes with chelatable zinc cations thereby inhibiting the cytotoxicity associated with excess chelatable zinc.

Compounds with chelation affinity and selectivity for first transition elements and their use in cosmetics and personal care products, inhibition of metalloenzymes, and inhibition of reperfusion injury

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, (2008/06/13)

This invention involves the use of a class of compounds with chelation affinity and selectivity for first transition series elements. Application or administration of the free or conjugated compound, or physiological salts of the free or conjugated compound, results in decrease of the bioavailability and/or chemical action of first transition series elements. These characteristics make such compounds useful in cosmetics and personal care products to decrease odor arising from microbial growth on body surfaces and in body cavities, decrease microbial growth on teeth, plaque, and gums that cause tooth decay and gum disease, inhibition of oxidative damage to the skin, inhibition of enzymatic action of metalloenzymes dependent on first transition series elements, and inhibition of reperfusion injury.

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