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O-(4-chlorophenyl) thiocarbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24641-61-0

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24641-61-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24641-61-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,6,4 and 1 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 24641-61:
(7*2)+(6*4)+(5*6)+(4*4)+(3*1)+(2*6)+(1*1)=100
100 % 10 = 0
So 24641-61-0 is a valid CAS Registry Number.

24641-61-0Relevant academic research and scientific papers

Green and efficient synthesis of thioureas, ureas, primary: O -thiocarbamates, and carbamates in deep eutectic solvent/catalyst systems using thiourea and urea

Bagherzadeh, Nastaran,Sardarian, Ali Reza,Inaloo, Iman Dindarloo

supporting information, p. 11852 - 11858 (2021/07/12)

An efficient and general catalysis process was developed for the direct preparation of various primary O-thiocarbamates/carbamates as well as monosubstituted thioureas/ureas by using thiourea/urea as biocompatible thiocarbonyl (carbonyl) sources. This procedure used choline chloride/tin(ii) chloride [ChCl][SnCl2]2 with a dual role as a green catalyst and reaction medium to afford the desired products in moderate to excellent yields. Moreover, the DES can be easily recovered and reused for seven cycles with no significant loss in its activity. Besides, the method shows very good performance for synthesizing the desired products on a large scale.

Synthesis and structure of substituted 5-phenoxy-1,2,4-dithiazole-3-ones

Ponomarov, Oleksandr,Padelkova, Zdenka,Hanusek, Jiri

experimental part, p. 1225 - 1228 (2012/01/04)

Seven new substituted 5-phenoxy-1,2,4-dithiazole-3-ones were prepared in modest yield (53-76%) from corresponding O-phenyl thiocarbamates and chlorocarbonylsulfenyl chloride in dry ether at-10 °C. All of the compounds were characterized by NMR and elemental analysis and some of them by X-ray diffraction. Preliminary kinetic measurements showed that the parent 5-phenoxy-1,2,4-dithiazole-3-one is a very efficient sulfurizing agent toward triphenyl phosphite. Copyright

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