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Benzenamine, 4-methoxy-N-[2,2,2-trifluoro-1-(trifluoromethyl)ethylidene]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

34025-21-3

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34025-21-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34025-21-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,0,2 and 5 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 34025-21:
(7*3)+(6*4)+(5*0)+(4*2)+(3*5)+(2*2)+(1*1)=73
73 % 10 = 3
So 34025-21-3 is a valid CAS Registry Number.

34025-21-3Relevant academic research and scientific papers

Aza-Henry Reaction with CF3-Ketimines: An Efficient Approach to Trifluoromethylated β-Nitroamines, 1,2-Diamines, α-Aminooximes, and Imidazolidinones

Kutovaya, Irina V.,Shmatova, Olga I.,Tkachuk, Viktor M.,Melnichenko, Nina V.,Vovk, Mikhail V.,Nenajdenko, Valentine G.

, p. 6749 - 6761 (2015/10/29)

CF3-Substituted ketimines synthesized from trifluoroacetone, hexafluoroacetone, and trifluoroacetophenones were studied in aza-Henry reactions with nitroalkanes. We found that nitromethane and nitropropane react with CF3-substituted

A novel route to dipeptides via noncondensation of amino acids: 2-Aminoperfluoropropene as a synthon for trifluoroalanine dipeptides

Guo, Yong,Fujiwara, Kana,Uneyama, Kenji

, p. 827 - 829 (2007/10/03)

2-Aminoperfluoropropene has been prepared by the Mg-promoted defluorinative N-silylation of N-p-methoxyphenyl hexafluoroacetone imine and has been employed as a synthon of trifluoroalanine for the preparation of trifluoroalanine dipeptides.

High-pressure 19F NMR study of the degenerate isomerization of hexafluoroacetone anils. Evidence for the existence of two different inversion transition states

Swaddle, Thomas W.,Doine, Hideo,Kinrade, Stephen D.,Sera, Akira,Asano, Tsutomu,Okada, Toshio

, p. 2378 - 2382 (2007/10/02)

Solvent, temperature, and pressure effects on the rate of the degenerate isomerization of hexafluoroacetone anils were studied by 19F NMR. The results unequivocally demonstrated that the mechanism is not rotation about the carbon-nitrogen bond

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