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Sulfoxylic diamide, bis(diphenylmethylene)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15972-30-2

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15972-30-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15972-30-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,9,7 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 15972-30:
(7*1)+(6*5)+(5*9)+(4*7)+(3*2)+(2*3)+(1*0)=122
122 % 10 = 2
So 15972-30-2 is a valid CAS Registry Number.

15972-30-2Downstream Products

15972-30-2Relevant academic research and scientific papers

On alkylideneamidosulfenyl chlorides and 1-thia-2-azoniaallene salts

Wirschun, Wolfgang G.,Hitzler, Martin G.,Jochims, Johannes C.,Groth, Ulrich

, p. 2627 - 2635 (2007/10/03)

X-Ray-diffraction analysis of 1Bu2C=N-SCl (4b) revealed an almost linear C=N=S unit with an S=N bond order of ca. 1.9 (Fig. 1), in agreement with the structure of a 1-thia-2-azoniaallene chloride. With SCl2 and SbCl5

Reaction of trithiazyl trichloride with alkenes and alkynes

Duan, Xiao-Guang,Duan, Xiao-Lan,Rees, Charles W.,Yue, Tai-Yuen

, p. 2597 - 2601 (2007/10/03)

Alkenes and alkynes react readily with trithiazyl trichloride 1 to give 1,2,5-thiadiazoles 2 in one step. Thus 3-amino-1,2,5-thiadiazole 5 is now readily available from N-vinylphthalimide and 1 in two steps. Cyclic alkenes react similarly to give fused thiadiazoles (7, 12) and phenanthrene gives the phenanthrothiadiazole 16. Tetra-substituted alkenes such as 13 appear to give the analogous 3,4-dihydrothiadiazoles (e.g. 14) which spontaneously ring open to give readily hydrolysed bis(methyleneamino) sulfides (e.g. 15). A simple set of mechanisms is proposed for all of these reactions.

Preparation, crystal and molecular structures of Ph2CNSNSO and a comparison of the -SNSO and -SNSS chromophores

Chivers, Tristram,Oakley, Richard T.,Pieters, Roger,Richardson, John F.

, p. 1063 - 1067 (2007/10/02)

The sulphenyl chloride, Ph2CNSCl, prepared in situ from Ph2CNSiMe3 and sulphur dichloride, has been employed in the synthesis of Ph2CNSNSO and Ph2CNSNSNSNCPh2 by reaction with Me3SiNSO and Me3SiNSNSiMe3, respectively.An X-ray structural determination of Ph2CNSNSO shows it to consist of a planar cis-trans chain.The crystals are triclinic and belong to the space group P1/, a = 9.9078(8), b = 10.0967(9), c = 15.1682(14) Angstroem, α = 78.646(7), β=71.065(7), γ = 63.449(7) deg, V = 1281.5(5) Angstroem3, Z = 4.The final R and Rw values were 0.033 and 0.027, respectively.The ?* ---> ?* excitation energies for the RSNSO and RSNSS chromophores are compared for different R groups and discussed in the light of MNDO calculations on the model compounds HSNSX (X = S, O).The thermal decomposition of both Ph2CNSNSO and Ph2CNSNSNSNCPh2 produced S4N4 and Ph2CO or (Ph2CN)2S, respectively.

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