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2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-(2,4,6-cycloheptatrien-1-ylidene)-1-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

593249-50-4

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593249-50-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 593249-50-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,9,3,2,4 and 9 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 593249-50:
(8*5)+(7*9)+(6*3)+(5*2)+(4*4)+(3*9)+(2*5)+(1*0)=184
184 % 10 = 4
So 593249-50-4 is a valid CAS Registry Number.

593249-50-4Downstream Products

593249-50-4Relevant academic research and scientific papers

Synthesis and properties of novel 5-(cyclohepta-2′, 4′,6′-trienylidene)pyrimidine-2(1H),4(3H),6(5H)-triones: Methodology for synthesizing cyclohepta[b]pyrimido[5,4-d]furan-8(7H),10(9H)-dionylium tetrafluoroborates

Naya, Shin-Ichi,Nitta, Makoto

, p. 3709 - 3718 (2003)

Novel condensation reaction of tropone with N-substituted and N,N′-disubstitued barbituric acids in Ac2O afforded 5-(cyclohepta-2′,4′,6′-trienylidene)pyrimidine-2(1H), 4(3H),6(5H)-trione derivatives (8a-f) in moderate to good yields. The 13C NMR spectral study of 8a-f revealed that the contribution of zwitterionic resonance structures is less important as compared with that of 8,8-dicyanoheptafulvene. The rotational barriers (ΔG?) around the exocyclic double bond of mono-substituted derivatives 8a-c were obtained to be 14.51-15.03kcalmol-1 by the variable temperature 1H NMR measurements. The electrochemical properties of 8a-f were also studied by CV measurement. Upon treatment with DDQ, 8a-c underwent oxidative cyclization to give two products, 7 and 9-substituted cyclohepta[b]pyrimido[5,4-d]furan-8(7H),10(9H)-dionylium tetrafluoroborates (11a-c·BF4- and 12a-c·BF4-) in various ratios, while that of disubstituted derivatives 8d-f afforded 7,9-disubstituted cyclohepta[b]pyrimido[5,4-d]furan-8(7H),10(9H)-dionylium tetrafluoroborate (11d-f·BF4-) in good yields. Similarly, preparation of known 5-(1′-oxocycloheptatrien-2′-yl)- pyrimidine-2(1H),4(3H),6(5H)-trione derivatives (14a-d) and novel derivatives 14e,f was carried out. Treatment of 14a-c with aq. HBF4/Ac2O afforded two kinds of novel products 11a-c·BF4- and 12a,c·BF4- in various ratios, respectively, while that of 14d-f afforded 11d-f. The product ratios of 11a-c·BF4- and 12a-c·BF4- observed in two kinds of cyclization reactions were rationalized on the basis of MO calculations of model compounds 20a and 21a. The spectroscopic and electrochemical properties of 11a-f·BF4- and 12a-c·BF4- were studied, and structural characterization of 11c·BF4- based on the X-ray crystal analysis and MO calculation was also performed.

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