52790-15-5 Usage
Uses
Used in Pharmaceutical Industry:
ETHYL 2-[(ETHOXYCARBONYL)THIO]ACETATE is used as a key intermediate in the synthesis of various pharmaceuticals due to its unique functional groups that facilitate chemical reactions required for drug development.
Used in Pesticide Production:
In the agrochemical sector, ETHYL 2-[(ETHOXYCARBONYL)THIO]ACETATE serves as an essential building block for the creation of pesticides, contributing to the development of effective crop protection agents.
Used in Flavoring Agents for Food Industry:
ETHYL 2-[(ETHOXYCARBONYL)THIO]ACETATE is used as a flavoring agent in the food industry, capitalizing on its mild, fruity odor to enhance the taste and aroma of various food products.
Used in Organic Synthesis:
ETHYL 2-[(ETHOXYCARBONYL)THIO]ACETATE is utilized as a versatile intermediate in organic synthesis, enabling the production of a wide range of fine chemicals for diverse applications across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 52790-15-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,7,9 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 52790-15:
(7*5)+(6*2)+(5*7)+(4*9)+(3*0)+(2*1)+(1*5)=125
125 % 10 = 5
So 52790-15-5 is a valid CAS Registry Number.
52790-15-5Relevant academic research and scientific papers
Reactions of Dithiocarbamates and Thiocarbonates with Heterocumulenes
Doelling, Wolfgang,Sperk, Katrin,Augustin, Manfred
, p. 671 - 678 (2007/10/02)
3,3-Bis(alkylthio)-2-dialkylaminothiocarbonylthioacrylonitriles 3-5 are obtained by dithiocarboxylation reaction of N,N-disubstituted S-cyanomethyl dithiocarbamates 1a-c in NaH/THF at -15 deg C followed by alkylation.Treatment of N,N-dimethyl-S-methylthiomethyldithiocarbamate 6 with CS2/2 n-BuLi in THF at -55 deg C gives N,N-dimethyl S-dithiocarbamates 7a-c.Phenylisothiocyanat reacts with S-alkoxycarbonylmethyl-O-alkylthiocarbonates 8a, b in the presence of t-BuOK/dry DMF to yield 4-subst. 2-oxo-3-phenyl-1,3-thiazoline-5-carboxylates 11a-e.
