10569-35-4 Usage
Uses
Used in Organic Synthesis:
2-Phenyl-3-(2-thienyl)acrylic acid serves as a key intermediate in organic synthesis, particularly for the creation of complex organic molecules that may have applications in various industries. Its unique structure allows for versatile chemical reactions, making it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 2-Phenyl-3-(2-thienyl)acrylic acid is utilized as a building block for the development of novel drug candidates. Its aromatic properties and conjugated system may contribute to the compound's biological activity, potentially leading to the discovery of new therapeutic agents with unique mechanisms of action.
Used in Material Sciences:
2-Phenyl-3-(2-thienyl)acrylic acid also finds applications in material sciences, where its aromatic and conjugated features can be exploited to develop new materials with specific properties. These materials could be used in the creation of advanced polymers, sensors, or other technological applications that benefit from the compound's chemical and physical characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 10569-35-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,6 and 9 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 10569-35:
(7*1)+(6*0)+(5*5)+(4*6)+(3*9)+(2*3)+(1*5)=94
94 % 10 = 4
So 10569-35-4 is a valid CAS Registry Number.
InChI:InChI=1/C13H10O2S/c14-13(15)12(9-11-7-4-8-16-11)10-5-2-1-3-6-10/h1-9H,(H,14,15)/p-1
10569-35-4Relevant academic research and scientific papers
CH?S hydrogen bonds as the organising force in 2,3-thienyl- and phenyl- or 2,3-dithienyl-substituted propenoic acid aggregates studied by the combination of FT-IR spectroscopy and computations
Csankó,Illés,Felf?ldi,Kiss,Sipos,Pálinkó
experimental part, p. 259 - 263 (2011/06/27)
Various propenoic acid stereoisomers 2,3-disubstituted with thienyl and/or phenyl groups were synthesised and their aggregation behaviour was studied both in solution and in the solid state by experimental (mid-range FT-IR spectroscopy) and computational
SYNTHESIS OF BENZOFURO- AND BENZOTHIENOPHENANTHRIDONES BY TWOFOLD PHOTOCHEMICAL DEHYDROCYCLIZATION REACTION
Karminski-Zamola, G.,Bajic, M.
, p. 1325 - 1334 (2007/10/02)
Four new N-(p-chlorophenyl)carboxamides 1 - 4 of 9-phenanthrene-, 5-naphthofuran-, and 5-naphtho- and 4-naphthothiophenecarboxylic acids have been synthesized.All carboxanilides were exposed to UV oxidative irradiation in methanolic solution.In the case of 2 and 3 corresponding benzo-furophenanthridin-10(9H)-one 5 and benzo-thienophenanthridin-10(9H)-one 6 are isolated.
SYNTHESIS OF (5-STYRYL-2-THIENYL)-PHENYLACRYLIC ACIDS
Karminski-Zamola, Grace,Bajic, Miro
, p. 1497 - 1501 (2007/10/02)
We describe the synthesis of E-3-(5-styryl-2-thienyl)-2-phenylacrylic acid 7, E-3-(5-styryl-2-thienyl)-2-(4-methoxyphenyl)acrylic acid 8, E-3--2-phenylacrylic acid 9 and E-3--2-(4
