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C-paranitrophenyl-N-phenylnitrilimine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

39143-47-0

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39143-47-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39143-47-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,1,4 and 3 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 39143-47:
(7*3)+(6*9)+(5*1)+(4*4)+(3*3)+(2*4)+(1*7)=120
120 % 10 = 0
So 39143-47-0 is a valid CAS Registry Number.

39143-47-0Relevant academic research and scientific papers

Regioselective 1,3-dipolar cycloaddition of nitrilimines to 2-methyl-2-vinyl oxirane

Yldrm, Muhammet,Dürüst, Yaar

experimental part, p. 3209 - 3215 (2011/05/30)

1,3-Dipolar cycloaddition of in situ generated C,N-diaryl nitrilimines to 2-methyl-2-vinyl oxirane gives rise to the regioselective formation of novel 5-(2-methyloxiranyl)-4,5-dihydropyrazole derivatives in moderate to good yields. The structures and ster

Synthesis of 1,3,4-thiadiazolines from 1,2-dithiole-3-thiones

Ogurtsov, Vladimir A.,Rakitin, Oleg A.,Rees, Charles W.,Smolentsev, Alexey A.

, p. 55 - 56 (2007/10/03)

The thiocarbonyl group of 4,5-dichloro-1,2-dithiole-3-thione reacts as a 1,3-dipolarophile towards diaryl nitrile imines by 1,3-dipolar cycloaddition followed by opening of the dithiole ring with loss of sulfur to give 5-methylene-1,3,4-thiadiazolines; th

Ketoken gem-dithiols and trithiones: Synthesis and study of the behavior towards dipole reagents; Synthesis of some nitrogen heteroaromatics

Zayed, Salem E.

, p. 7 - 13 (2007/10/03)

The behavior of ketoken gem-dithiols towards active methylene and methyl groups resulted in the formation of thiopyrano-dihydrocaumarine derivatives IIIa,b via cyclocondensation reaction between substituted 4-dihydrocyclohexanone Ia.b. N-phenylpyrazoline

Photochemistry of Diarylsubstituted 2H-Tetrazoles, XI and Sydnones. V. Flashphotolytic Investigations with 2,5-Diaryl-2H-tetrazoles and 3,4-Diarylsydnones. Absolute Rate Constants of Cycloadditionreactions of Diarylnitrile Imines to Dipolarophils

Leihkauf, P.,Lohse, V.,Csongar, Ch.,Tomaschewski, G.

, p. 789 - 798 (2007/10/02)

The flash photolysis of 2,5-Diaryl-2H-tetrazoles 1 and 3,4-Diarylsydnones 2 was investigated.The nitrile imines were detected spectroscopically as short living intermediates.Rate constants of the cycloaddition reaction of nitrile imines and dipolarophiles

Photochemistry of Diarylsubstituted 2H-Tetrazoles. II. The Influence of the Substituents on the Absorption Properties of Diarylsubstituted Nitrilimines

Csongar, Ch.,Leihkauf, P.,Lohse, V.,Tomaschewski, G.

, p. 96 - 102 (2007/10/02)

Irradation of 2,5-diaryl-2H-tetrazoles in an EPA-glass (ether: i-pentan: ethanol = 5:5:2) or in an i-pentan glass at 77-80 K with UV-light of wavelength 290 nm yields diarylnitrilimines by the extrusion of nitrogen.The photoreactions investigated show spe

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