25858-77-9 Usage
Uses
Used in Pharmaceutical Industry:
(2E)-3-(carbamothioylsulfanyl)prop-2-enoic acid is used as a key intermediate in the synthesis of pharmaceuticals for its ability to form carbon-carbon and carbon-sulfur bonds, contributing to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, (2E)-3-(carbamothioylsulfanyl)prop-2-enoic acid serves as a crucial building block in the creation of various agrochemicals, such as pesticides and herbicides, due to its reactive nature and capacity to form essential chemical linkages.
Used in Material Science:
(2E)-3-(carbamothioylsulfanyl)prop-2-enoic acid is utilized in the development of new materials, capitalizing on its functional groups and reactivity to engineer innovative compounds with unique properties for various applications.
Used in Industrial Processes:
(2E)-3-(carbamothioylsulfanyl)prop-2-enoic acid also has potential applications in the optimization and development of new industrial processes, where its reactive intermediate capabilities can enhance the efficiency and effectiveness of chemical reactions in manufacturing.
Check Digit Verification of cas no
The CAS Registry Mumber 25858-77-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,8,5 and 8 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 25858-77:
(7*2)+(6*5)+(5*8)+(4*5)+(3*8)+(2*7)+(1*7)=149
149 % 10 = 9
So 25858-77-9 is a valid CAS Registry Number.
25858-77-9Relevant academic research and scientific papers
The Tautomeric Equilibria of Thio Analogues of Nucleic Acid Bases. Part 1. 2-Thiouracil: Background, Preparation of Model Compounds, and Gas-phase Proton Affinities
Katritzky, Alan R.,Baykut, Gokhan,Rachwal, Stanislaw,Szafran, Miroslaw,Caster, Kenneth C.,Eyler, John
, p. 1499 - 1506 (2007/10/02)
The preparation is reported of all four the monoalkyl derivatives of 2-thiouracil and four of the six possible dialkyl derivatives required as models for a study of the tautomeric equilibria by physical methods.Gas-phase proton affinities are determined using ion cyclotron resonance mass spectrometry, and are used to provide quantitative estimates of individual tautomer stabilities in the vapour state.These quantitative results agree well with qualitative deductions of predominant structures for the monoalkyl derivatives from i.r. spectroscopy.
