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N-phenyl-N-(3-phenyl-1,3-thiazolidin-2-ylidene)amine is a complex organic compound with the molecular formula C18H14N2S. It is characterized by a phenyl group attached to a nitrogen atom, which is in turn connected to a 1,3-thiazolidin-2-ylidene ring system. This ring system features a sulfur atom and a phenyl group, with the phenyl group being part of the 3-position on the thiazolidine ring. The compound is known for its potential applications in the synthesis of various pharmaceuticals and chemical intermediates, particularly in the area of heterocyclic chemistry. Its structure and properties make it a valuable component in the development of new drugs and materials.

6200-49-3

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6200-49-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6200-49-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,0 and 0 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6200-49:
(6*6)+(5*2)+(4*0)+(3*0)+(2*4)+(1*9)=63
63 % 10 = 3
So 6200-49-3 is a valid CAS Registry Number.

6200-49-3Downstream Products

6200-49-3Relevant academic research and scientific papers

Synthesis of thiazolidinimines/thiazinan-2-imines via three-component coupling of amines, vic-dihalides and isothiocyanates under metal-free conditions

Kumar, Rahul,Joshi, Abhisek,Rawat, Deepa,Adimurthy, Subbarayappa

supporting information, p. 1340 - 1352 (2021/02/22)

An expeditious approach for the synthesis of thiazolidin-2-imines and 1,3-thiazinan-2-imines through three-components coupling (TCC) of amines, isothiocynates and dihalides under metal-free conditions has been described. Dichloroethane (DCE) employed as two carbon (C2) source for the annulation and obtained saturated five membered heterocycles.With 1,3-dibromopropane, six membered heterocycles were obtained in good yields. The metal-free, broad substrate scope, functional group tolerance and applicability at gram scale synthesis are the advantages of the present protocol.

Regioselective Cycloaddition of 1,2-Disubstituted Aziridines to Heterocumulenes Catalyzed by Organoantimony Halides

Nomura, Ryoki,Nakano, Takahiro,Nishio, Yoshitaka,Ogawa, Sachiko,Ninagawa, Akira,Matsuda, Haruo

, p. 2407 - 2410 (2007/10/02)

In the presence of catalytic amounts of organoantimony(V) halides such as Ph4SbI, Ph4SbBr, Ph3SbBr2, and Ph3SbCl2, the cycloaddition of aziridines 1a-g with heterocumulenes (phenyl isothiocyanate, carbon disulfide, and carbon dioxide) selectively gave ring-expanded cycloadducts 3a-d, f, g and 6e by α-cleavage of the aziridine rings. - Key Words: Organoantimony halides / Aziridines, cycloaddition of, α-cleavage of / Heterocumulenes

The Preparation of Cyclic Dithia and Thiaza Compounds by the Reaction of Potassium Carbonate with Heterocumulenes and Alkylene Dibromides or Carbonate Catalyzed by Organostannyl Compounds

Fujinami, Tatsuo,Sato, Shinichi,Uchida, Norimasa,Sakai, Shizuyoshi

, p. 1174 - 1177 (2007/10/02)

Cyclic 1,3-dithia- and 1,3-thiaza-2-ylidene compounds were obtained by the heterogenous reaction of solid potassium carbonate, a sulfur-containing heterocumulene, such as aryl isothiocyanate, carbon disulfide, or carbonyl silfide, and alkylene dibromides or ethylene carbonate in the presence of bis(tributylstannyl) compounds.The effect of an organostannyl catalyst on these reactions is discussed.

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