80737-85-5 Usage
Description
[(2-oxo-2-phenylethyl)sulfanyl]acetonitrile, with the molecular formula C10H9NO2S, is a chemical compound that belongs to the class of nitriles. It features a phenyl group and a thioether group, which contribute to its unique chemical properties and potential applications in various fields.
Uses
Used in Pharmaceutical Industry:
[(2-oxo-2-phenylethyl)sulfanyl]acetonitrile is used as a building block in the synthesis of various pharmaceuticals. Its unique structure allows for the creation of a wide range of compounds with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, [(2-oxo-2-phenylethyl)sulfanyl]acetonitrile is utilized as a starting material for the development of new agrochemicals, such as pesticides and herbicides, due to its versatile chemical structure.
Used in Organic Synthesis:
[(2-oxo-2-phenylethyl)sulfanyl]acetonitrile is also employed in organic synthesis as an intermediate for the production of various organic compounds, taking advantage of its reactive functional groups.
Used in Cancer Research:
[(2-oxo-2-phenylethyl)sulfanyl]acetonitrile is being studied for its potential anti-cancer properties. Its biological activity is of interest to researchers, who are investigating its effects on cancer cells and its potential role in the development of new cancer treatments.
Used in Inflammation Research:
Additionally, [(2-oxo-2-phenylethyl)sulfanyl]acetonitrile is being explored for its anti-inflammatory properties, which could lead to its use in the development of new treatments for inflammatory conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 80737-85-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,7,3 and 7 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 80737-85:
(7*8)+(6*0)+(5*7)+(4*3)+(3*7)+(2*8)+(1*5)=145
145 % 10 = 5
So 80737-85-5 is a valid CAS Registry Number.
80737-85-5Relevant articles and documents
Continuous Flow Synthesis of 2H-Thiopyrans via thia-Diels–Alder Reactions of Photochemically Generated Thioaldehydes
Sachse, Florian,Gebauer, Konrad,Schneider, Christoph
supporting information, p. 64 - 71 (2020/11/30)
Herein, we report a novel protocol for the photochemical generation of thioaldehydes in a continuous flow process which were in situ reacted with electron rich 1,3-butadienes in thia-Diels–Alder reactions. A broad range of 3,6-dihydro-2H-thiopyrans were formed as products in much higher yields and productivities as compared to classical batch processes. Moreover, greatly reduced reaction times and a facile large-scale preparation of products were achieved by fully exploiting the advantages of continuous flow technology.
Thioaldehyde Diels-Alder Reactions
Vedejs, E.,Eberlein, T. H.,Mazur, D. J.,McClure, C. K.,Perry, D. A.,et al.
, p. 1556 - 1562 (2007/10/02)
Thioaldehydes containing virtually any α-substitutent can be generated by photofragmentation of phenacyl sulfides.Donor-substituted derivatives are reactive toward electron-rich dienes and give 2 + 4 cycloadducts with regiochemistry corresponding to advan
Dienophilic Thioaldehydes
Vedejs, E.,Eberlein, T. H.,Varie, D. L.
, p. 1445 - 1447 (2007/10/02)
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