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Ethyl (methylsulfanyl)carbamate, also known as ethyl methanethiocarbamate, is an organic compound with the chemical formula C4H9NOS. It is a colorless liquid with a pungent odor and is soluble in water. ethyl (methylsulfanyl)carbamate is primarily used as a pesticide, specifically as a fungicide, to protect crops from various fungal diseases. It works by inhibiting the growth and development of fungi, thereby preventing them from causing damage to plants. Ethyl (methylsulfanyl)carbamate is also known for its potential to be toxic to humans and animals if ingested or inhaled, and it is important to handle it with care and follow safety guidelines.

817-73-2

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817-73-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 817-73-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,1 and 7 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 817-73:
(5*8)+(4*1)+(3*7)+(2*7)+(1*3)=82
82 % 10 = 2
So 817-73-2 is a valid CAS Registry Number.

817-73-2Relevant academic research and scientific papers

A synthesis of N-alkyl and N,N-dialkyl O-ethyl thiocarbamates from diethyl dixanthogenate using different oxidants

Milosavljevic, Milutin M.,Sovrlic, Milica,Marinkovic, Aleksandar D.,Milenkovic, Dragan D.

experimental part, p. 749 - 755 (2011/07/08)

A novel synthesis of N-alkyl and N,N-dialkyl O-ethyl thiocarbamates from diethyl dixanthogenate and primary and secondary amines, using three oxidizing systems, has been developed on the laboratory scale, and the method using sodium hypochlorite has been applied on a semi-industrial scale. The effect of the oxidizing agents, sodium hypochlorite, in-situ-generated peracetic acid, and the manganese(II) acetate/oxygen system on product purity and yield was studied. The results obtained by use of these three methods were compared with those obtained by reaction of sodium ethyl xanthogenacetate and amines, and of sodium ethyl xanthate with amines in the presence of sulfated nickel zeolite catalyst. The reaction mechanism of sodium hypochlorite oxidation has been established on the basis of isolation of reaction intermediates and determination of their structure by use of Fourier-transform infrared, 1H and 13C NMR, and mass spectrometric methods. The suggested sodium hypochlorite and manganese(II) acetate/oxygen systems have many advantages in comparison with commercial and catalytically promoted synthetic methods, because they are new ecologically friendly syntheses. Springer-Verlag 2010.

Cycloaddition of new N-unsubstituted azomethine ylides generated from N-[(trimethylsilyl)methyl]thiocarbamates, synthetic equivalents of nonstabilized alkoxy- or alkylthionitrile ylides

Tsuge, Otohiko,Hatta, Taizo,Shinozuka, Masanori,Tashiro, Hideki

, p. 249 - 254 (2007/10/03)

The reaction of (trimethylsilyl)methyl isothiocyanate with alcohol in the presence of aluminum alkoxide provides a useful route for the preparation of N-[(trimethylsilyl)methyl]thiocarbamates. The S-methylation of thiocarbamates followed by desilylation g

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