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1,2,4-Triazolidine-3,5-dione, 4-phenyl-1-(2-propenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73970-92-0

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73970-92-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73970-92-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,9,7 and 0 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 73970-92:
(7*7)+(6*3)+(5*9)+(4*7)+(3*0)+(2*9)+(1*2)=160
160 % 10 = 0
So 73970-92-0 is a valid CAS Registry Number.

73970-92-0Relevant academic research and scientific papers

Ene Reactions of Allylic Derivatives of Silicon, Germanium, Tin and Lead with N-Phenyltriazolinedione: the Effect of Varying the Metal

Cai, Jiaqiang,Davies, Alwyn G.

, p. 1743 - 1746 (2007/10/02)

The compounds Ph3MCH2CH=CH2 and (M=Si, Ge, Sn or Pb) have been treated with 4-phenyl-1,2,4-triazoline-3,5-dione, and the relative yields of the products of the M-ene reaction, of the H-ene reaction, and of the reaction involving cycloaddition with shift of the organometallic substituent, have been determined.The silicon compounds react principally by the H-ene process.The cycloaddition process is at a maximum (50percent or 70percent) with the germanium compounds, and the tin compounds show mainly the M-ene reaction, with some cycloaddition but no H-ene reaction.Triphenylprop-2-enylplumbane show only the M-ene reaction.In trimethyl(1,1-dimethylprop-2-enyl)silane, in which the H-ene reaction is blocked, only cycloaddition with shift of the silyl group is observed.

Ene Reactions of Allylic Tin Compounds with Singlet Oxygen and with 4-Phenyl-1,2,4-triazoline-3,5-dione

Dang, Hai-Shan,Davies, Alwyn G.

, p. 2011 - 2020 (2007/10/02)

Allylic tin compounds (I) react with singlet oxygen to give allylperoxystannyl compounds (II) by stannylallylation, stannylallyl hydroperoxides (III) by hydroallylation, and 4-stannyl-1,2-dioxolanes (IV) by rearrangement and cycloaddition.For example, 3-t

Reactions of Allylsilanes with 4-Substituted 1,2,4-Triazoline-3,5-diones

Ohashi, Shinichi,Ruch, Wayne E.,Butler, George B.

, p. 614 - 619 (2007/10/02)

The reaction between allyltrimethylsilane (1) and 4-phenyl-1,2,4-triazoline-3,5-dione (2) was studied, and the structures of three products were determined by using 1H NMR, 13C NMR, and mass spectra.The effects of solvent and temperature on the relative yields of products were studied, and a reaction mechanism involving an ionic intermediate was suggested.The mechanism of the reaction between diallyldimethylsilane (3) with triazolinediones was found to be quite similar to that of 1.

Ene Reaction of Triazolinediones with Alkenes. 1. Structure and Properties of Products

Ohashi, Shinichi,Leong, Koon-wah,Matyjaszewski, Kristoff,Butler, George B.

, p. 3467 - 3471 (2007/10/02)

The structures of ene products from reaction of triazolinediones with alkenes and polyisoprene were studied by using (1)H NMR.The pKa values of the ene products were measured.The reactivity and stability of the ene products were also studied.

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