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N-(m-methylphenyl)-N'-(4-phenylthiazol-2-yl)thiocarbamide is a complex organic compound with the chemical formula C18H15N3S. It is a derivative of thiocarbamide, featuring a methylphenyl group attached to the nitrogen atom and a phenylthiazol-2-yl group connected to the other nitrogen atom. N-(m-methylphenyl)-N'-(4-phenylthiazol-2-yl)thiocarbamide is characterized by its unique molecular structure, which includes a thiocarbonyl group (C=S) and a thiazole ring. It is primarily used in chemical research and as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Due to its specific structure, it may exhibit unique properties and reactivity, making it a valuable compound for exploring new chemical reactions and applications in the fields of chemistry and materials science.

2982-44-7

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2982-44-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2982-44-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,8 and 2 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2982-44:
(6*2)+(5*9)+(4*8)+(3*2)+(2*4)+(1*4)=107
107 % 10 = 7
So 2982-44-7 is a valid CAS Registry Number.

2982-44-7Relevant academic research and scientific papers

Reaction of Isothiocyanates with Thiourea--a Correction

Joshua, Chittoor P.,Prasannan, E.,Thomas, Saramma K.

, p. 917 - 921 (2007/10/02)

The condensation products of isothiocyanates with thiourea reported to be S-(N-substituted thiocarbamoyl)isothioureas are in fact 1-substituted 2,4-dithiobiurets and not the former.The condensation of isothiocyanates with 1-substituted thioureas also is f

Synthesis of 2-(4',5'-disubstituted-thiazol-2'-ylimino)-3-(m-methylphenyl)-5-methyl (or H)-4-thiazolidinones and Their Fungicidal Activity

Bhargava, P. N.,Prakash, Shree,Lakhan, Ram

, p. 927 - 929 (2007/10/02)

A number of 2-(4',5'-disubstituted-thiazol-2'-ylimino)-3-(m-methylphenyl)-5-methyl (or H)-4-thiazolidinones (I) have been synthesised and screened for their antifungal activity against Alternaria tenuis at different concentrations.None of the compounds sh

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