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Thiourea, N-2-benzothiazolyl-N'-(4-chlorophenyl)-, also known as 2-(4-chlorophenyl)-N-(benzothiazol-2-yl)thiourea, is an organic compound with the chemical formula C14H9ClN2S2. It is a derivative of thiourea, featuring a benzothiazolyl group and a 4-chlorophenyl group attached to the nitrogen atoms. Thiourea, N-2-benzothiazolyl-N'-(4-chlorophenyl)- is primarily used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its unique structure, it exhibits specific reactivity and properties that make it valuable in the development of new compounds with potential applications in various industries.

1820-05-9

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1820-05-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1820-05-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,2 and 0 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1820-05:
(6*1)+(5*8)+(4*2)+(3*0)+(2*0)+(1*5)=59
59 % 10 = 9
So 1820-05-9 is a valid CAS Registry Number.

1820-05-9Relevant academic research and scientific papers

Synthesis and cytotoxic evaluation of thiourea and N-bis-benzothiazole derivatives: A novel class of cytotoxic agents

Kumbhare, Ravindra M.,Dadmal, Tulshiram,Kosurkar, Umesh,Sridhar,Rao, J. Venkateswara

supporting information; experimental part, p. 453 - 455 (2012/02/16)

Benzothiazolyl thiocarbamides has been achieved using a catalytic amount of 4-dimethylaminopyridine (DMAP) followed by its chemoselective oxidative cyclization with 1,3-di-n-butylimidazolium tribromide[bbim][Br3] to afford the N-bis-benzothiazole derivatives. All the synthesized compounds were evaluated for cytotoxic activity against two human monocytic cell lines (U 937, THP-1) and a mouse melanoma cell line (B16-F10). Based on their IC50 values, the majority of the benzothiazolyl thiocarbamides and N-bis-benzothiazoles had significant antiproliferative activity on U 937 and B16-F10 cells, the compounds 3b, 3e, 3f, 3k, 6c and 6h were found to be the most active. The present findings indicate clearly that the compound 3e exhibited more antiproliferative activity on U 937 cells than the standard molecule, etoposide. Nevertheless, these compounds have shown comparatively less cytotoxicity towards THP-1 cells.

1,3-Di-n-butylimidazolium tribromide-mediated chemoselective oxidative cyclization of benzothiazoyl carbaimides: A novel approach toward the synthesis of N-bis-benzothiazole derivatives

Kumbhare, Ravindra M.,Dadmal, Tulshiram,Kosurkar, Umesh,Vijay Kumar

experimental part, p. 342 - 348 (2012/06/15)

4-(N,N-Dimethylamino)pyridine is found to be an efficient catalyst for the synthesis of benzothiazoyl carbaimide derivatives using 2-aminobenzothiazoles and phenylisothiocyanates, which on treatment with ionic liquid [bbim][Br 3] at 70°C afforded exclusive formation of N-bis-benzothiazole derivatives in good yield. Copyright

Solvent-free synthesis of heterocyclic thioureas using microwave technology

Li, Jian-Ping,Luo, Qian-Fu,Wang, Yu-Lu,Wang, Hong

, p. 73 - 75 (2007/10/03)

A new and rapid solvent-free synthesis of heterocyclic thioureas in a microwave oven has been reported for the first time. Nine heterocyclic thioureas that possess biological activity have been synthesized. The reaction time is short (2-4.5 min) and gives

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