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N,N'-bis(o-phenylphenyl)formamidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

115293-11-3

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115293-11-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 115293-11-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,2,9 and 3 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 115293-11:
(8*1)+(7*1)+(6*5)+(5*2)+(4*9)+(3*3)+(2*1)+(1*1)=103
103 % 10 = 3
So 115293-11-3 is a valid CAS Registry Number.

115293-11-3Relevant academic research and scientific papers

Ring-expanded iridium and rhodium N-heterocyclic carbene complexes: a comparative DFT study of heterocycle ring size and metal center diversity

Karaca,Akko?,?z,Altin,Dorcet,Roisnel,Gürbüz,?elik,Bayri,Bruneau,Ya?ar,?zdemir

, p. 1270 - 1284 (2017)

A new series of ring-expanded six- and seven-membered N-heterocyclic carbene precursors (re-NHCs) and their transition metal complexes were synthesized. The basic properties of the synthesized materials were investigated by density functional theory (DFT)

Synthesis and structural characterisation of heavy alkaline earth N,N′-bis(aryl)formamidinate complexes

Cole, Marcus L.,Deacon, Glen B.,Forsyth, Craig M.,Konstas, Kristina,Junk, Peter C.

, p. 3360 - 3367 (2006)

Treatment of calcium or strontium with 2.0 equivalents of N,N′-bis(o-methylphenyl)formamidine (o-TolFormH), N,N′-bis(2,6-dimethylphenyl)formamidine (XylFormH) or N,N′-bis(o-phenylphenyl)formamidine (o-PhPhFormH) in the presence of 1.0 equivalent of Hg(Cs

Facile synthesis of hydroxyformamidines by the N-oxidation of their corresponding formamidines

Cibian, Mihaela,Langis-Barsetti, Sophie,Hanan, Garry S.

supporting information; experimental part, p. 405 - 409 (2011/04/22)

The N-oxidation of N,N-disubstituted amidines with MCPBA (m-chloroperoxibenzoic acid) affords a mild, rapid, and efficient route to the corresponding hydroxyamidines This novel synthetic route for the preparation of N,N-disubstituted hydroxyamidines provi

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