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(E)-5-(4-methylpyridin-2-yl)-2-phenyl-3-(phenylimino)-1,2,5-oxadiazinan-4-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1092459-69-2

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1092459-69-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1092459-69-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,2,4,5 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1092459-69:
(9*1)+(8*0)+(7*9)+(6*2)+(5*4)+(4*5)+(3*9)+(2*6)+(1*9)=172
172 % 10 = 2
So 1092459-69-2 is a valid CAS Registry Number.

1092459-69-2Downstream Products

1092459-69-2Relevant academic research and scientific papers

Mechanisms of reactions conducted on α-amido-α-aminonitrones, determined based on the structures of their crystalline products and DFT calculations

Trzewik, Bartosz,Seidler, Tomasz,Broclawik, Ewa,Stadnicka, Katarzyna

scheme or table, p. 2220 - 2228 (2011/01/10)

The crystal structures of several compounds obtained from recently synthesised α-amido-α-aminonitrones were determined by X-ray diffraction. The compounds belonged to three different classes: 1,2,5-oxadiazin-4-ones, amidines and dibenzo[d,f][1,3]diazepine

New α-amido-α-aminonitrones as building blocks for constructing heterocyclic systems

Trzewik, Bartosz,Ciez, Dariusz,Hodorowicz, Maciej,Stadnicka, Katarzyna

experimental part, p. 2977 - 2985 (2009/04/05)

New, stable α-amido-α-aminonitrones were obtained in good yields from 3-oxobutyric acid N-pyridin-2-ylamides and nitrosobenzene. The α-amido-α-aminonitrones were then used as new, versatile building blocks to obtaining various heterocycles with both bielectrophilic and binucleophilic reagents. With diiodomethane as reagent, 1,2,5-oxadiazine derivatives were formed, whereas reactions with aromatic 1,2-, 1,3- and 1,4-diamines yielded quinoxaline, quinazoline, perimidine, and dibenzo[d,f][1,3]diazepine derivatives, respectively. Georg Thieme Verlag Stuttgart.

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