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Pd(phenylazopyridine)(3,5-di-tert-butylcatecholate) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

180334-31-0

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180334-31-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 180334-31-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,0,3,3 and 4 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 180334-31:
(8*1)+(7*8)+(6*0)+(5*3)+(4*3)+(3*4)+(2*3)+(1*1)=110
110 % 10 = 0
So 180334-31-0 is a valid CAS Registry Number.

180334-31-0Downstream Products

180334-31-0Relevant academic research and scientific papers

Isomeric separation in donor-acceptor systems of Pd(ii) and Pt(ii) and a combined structural, electrochemical and spectroelectrochemical study

Deibel, Naina,Schweinfurth, David,Fiedler, Jan,Zali, Stanislav,Sarkar, Biprajit

, p. 9925 - 9934 (2011/12/16)

Compounds of the form [(pap)M(Q2-)] (pap = phenylazopyridine; Q = 3,5-di-tert-butyl-benzoquinone, M = Pd, 1a and 1b, M = Pt, 2a and 2b; Q = 4-tert-butyl-benzoquinone, M = Pd, 3a and 3b; M = Pt, 4a and 4b) were synthesized in a one-pot reaction.

Synthesis, spectral and electrochemical studies of arylazopyridine complexes of palladium(II) with dioxolenes

Roy, Ramkrishna,Chattopadhyay, Pabitra,Sinha, Chittaranjan,Chattopadhyay, Surajit

, p. 3361 - 3370 (2008/10/09)

Mixed-ligand complexes of the formula Pd(aap)(OO) (5-8), where aap=2-(arylazo)-pyridines and oo=dioxolanes, viz. catechol (CATH2), 4-tert-butyl catechol (TBCATH2), 3,5-di-tert-butylcatechol (DTBCATH2), and 2,3-dihydroxynaphthalene (DHN), were prepared and characterized by elemental analyses, IR, UV-vis and (1)H NMR data. Cyclic voltammograms suggest four successive one-electron responses and are highly sensitive to the nature ofsubstituents. These complexes were found to show a ligand-to-ligand cha rge transfer (LLCT) band. THe position of the LLCT band is largely dependent on the substituent type on the catechol frame and is qualitatively assigned as the 3b1(cat).fwadrw.π*(aap) transition.

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