62455-63-4 Usage
Uses
Used in Organic Synthesis:
2-(4-METHOXYBENZOYL)-3,3-DI(METHYLTHIO)ACRYLONITRILE is used as a key intermediate in organic synthesis for its ability to participate in various chemical reactions, facilitating the creation of a wide range of compounds.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 2-(4-METHOXYBENZOYL)-3,3-DI(METHYLTHIO)ACRYLONITRILE is used as a building block for the development of new drugs, contributing to the synthesis of active pharmaceutical ingredients.
Used in Agrochemicals:
2-(4-METHOXYBENZOYL)-3,3-DI(METHYLTHIO)ACRYLONITRILE is utilized as a precursor in the production of agrochemicals, playing a role in the synthesis of compounds that protect crops from pests and diseases.
Used in Dye Manufacturing:
2-(4-METHOXYBENZOYL)-3,3-DI(METHYLTHIO)ACRYLONITRILE is also used in the dye industry as a starting material for the synthesis of various dyes, which are essential for coloring textiles, plastics, and other materials.
Used in Material Science:
2-(4-METHOXYBENZOYL)-3,3-DI(METHYLTHIO)ACRYLONITRILE shows potential as a precursor for the synthesis of novel materials, which could have applications in various fields such as electronics, coatings, and advanced materials.
Used in Drug Discovery:
In the field of drug discovery, 2-(4-METHOXYBENZOYL)-3,3-DI(METHYLTHIO)ACRYLONITRILE is used as a component in compound libraries, aiding researchers in identifying new therapeutic agents through high-throughput screening processes.
Check Digit Verification of cas no
The CAS Registry Mumber 62455-63-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,4,5 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 62455-63:
(7*6)+(6*2)+(5*4)+(4*5)+(3*5)+(2*6)+(1*3)=124
124 % 10 = 4
So 62455-63-4 is a valid CAS Registry Number.
InChI:InChI=1/C13H13NO2S2/c1-16-10-6-4-9(5-7-10)12(15)11(8-14)13(17-2)18-3/h4-7H,1-3H3
62455-63-4Relevant academic research and scientific papers
ALKYLIERUNGS- AND ARYLIERUNGSREAKTIONEN MIT GEMINALEN DITHIOLATEN
Rudorf, W. D.,Augustin, M.
, p. 329 - 336 (2007/10/02)
Acyl acetonitriles 1 react with carbon disulfide in the presence of sodium hydride to give disodium salts 2.Treatment of 2 with an alkylation reagent yields the open chain or cyclic acyl cyanketene S,S-acetals 3,4,8 and 10, respectively.Arylation to 11 is successful with 2,4-dinitro-chlorobenzene.Adding only one equivalent of methyl iodide to 2 and acidifying the reaction mixture lead to the monoalkylated compounds 7, whereas β-hydroxythioanilides 12 are available by reaction of 1 with phenyl isothiocyanate.A comparison of the ?-values shows that there exists the same type of the proton's chelation of the OH-group in 7 and 12.
