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Ethyl bis(propylsulfanyl)carbamate is a chemical compound with the molecular formula C8H18S4NO2. It is an organosulfur compound, characterized by the presence of two propylsulfanyl groups (-SCH2CH2CH3) attached to a central carbamate group (-NHCOO). The carbamate group is derived from the reaction of isocyanate with an alcohol, in this case, ethanol (ethyl group). ethyl bis(propylsulfanyl)carbamate is known for its potential applications in various chemical processes and as a precursor in the synthesis of other organic compounds. It is important to note that handling and usage of such chemicals should be done with caution, adhering to safety protocols due to their potential reactivity and toxicity.

1975-85-5

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1975-85-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1975-85-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,7 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1975-85:
(6*1)+(5*9)+(4*7)+(3*5)+(2*8)+(1*5)=115
115 % 10 = 5
So 1975-85-5 is a valid CAS Registry Number.

1975-85-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name O-ethyl N,N-dipropylcarbamothioate

1.2 Other means of identification

Product number -
Other names O-Ethyl dipropylthiocarbamate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1975-85-5 SDS

1975-85-5Downstream Products

1975-85-5Relevant 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.

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