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1H,1'H-5,5'-bibenzotriazole is a chemical compound with the molecular formula C12H8N6. It is a white crystalline solid that is soluble in water and various organic solvents. 1H,1'H-5,5'-bibenzotriazole is primarily used as a corrosion inhibitor, particularly in the automotive and aerospace industries, to protect metal surfaces from rust and other forms of corrosion. It is also employed as a stabilizer in various chemical processes, such as the production of polyurethane foams, where it helps to prevent the breakdown of the foam. Additionally, 1H,1'H-5,5'-bibenzotriazole is used in the synthesis of other chemicals and as a reagent in analytical chemistry. Its stability, effectiveness, and low toxicity make it a valuable compound in industrial applications.

15805-13-7

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15805-13-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15805-13-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,8,0 and 5 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 15805-13:
(7*1)+(6*5)+(5*8)+(4*0)+(3*5)+(2*1)+(1*3)=97
97 % 10 = 7
So 15805-13-7 is a valid CAS Registry Number.

15805-13-7Upstream product

15805-13-7Downstream Products

15805-13-7Relevant academic research and scientific papers

Using Postsynthetic X-Type Ligand Exchange to Enhance CO2Adsorption in Metal-Organic Frameworks with Kuratowski-Type Building Units

Bien, Caitlin E.,Cai, Zhongzheng,Wade, Casey R.

, p. 11784 - 11794 (2021)

Postsynthetic modification methods have emerged as indispensable tools for tuning the properties and reactivity of metal-organic frameworks (MOFs). In particular, postsynthetic X-type ligand exchange (PXLE) at metal building units has gained increasing attention as a means of immobilizing guest species, modulating the reactivity of framework metal ions, and introducing new functional groups. The reaction of a Zn-OH functionalized analogue of CFA-1 (1-OH, Zn(ZnOH)4(bibta)3, where bibta2- = 5,5′-bibenzotriazolate) with organic substrates containing mildly acidic E-H groups (E = C, O, N) results in the formation of Zn-E species and water as a byproduct. This Br?nsted acid-base PXLE reaction is compatible with substrates with pKa(DMSO) values as high as 30 and offers a rapid and convenient means of introducing new functional groups at Kuratwoski-type metal nodes. Gas adsorption and diffuse reflectance infrared Fourier transform spectroscopy experiments reveal that the anilide-exchanged MOFs 1-NHPh0.9 and 1-NHPh2.5 exhibit enhanced low-pressure CO2 adsorption compared to 1-OH as a result of a Zn-NHPh + CO2 ? Zn-O2CNHPh chemisorption mechanism. The MFU-4l analogue 2-NHPh ([Zn5(OH)2.1(NHPh)1.9(btdd)3], where btdd2- = bis(1,2,3-triazolo)dibenzodioxin), shows a similar improvement in CO2 adsorption in comparison to the parent MOF containing only Zn-OH groups.

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