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(Z)-2,3-di(thiophen-2-yl)acrylic acid is an organic compound characterized by its unique structure, featuring a central acrylic acid backbone with two thiophene rings attached at the 2 and 3 positions. Thiophene is a heterocyclic compound with a sulfur atom in the ring, which imparts distinct electronic and steric properties to the molecule. This chemical is of interest in the field of materials science, particularly for its potential applications in the development of organic electronics, such as in the design of novel semiconductors and conductive polymers. The (Z)-isomer specification indicates the geometric arrangement of the thiophene rings relative to the double bond in the acrylic acid moiety, which can significantly influence the compound's reactivity and physical properties.

716-33-6

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716-33-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 716-33-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,1 and 6 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 716-33:
(5*7)+(4*1)+(3*6)+(2*3)+(1*3)=66
66 % 10 = 6
So 716-33-6 is a valid CAS Registry Number.

716-33-6Relevant 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

, p. 259 - 263 (2011)

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 some new bis-(p-fluorophenyl)amides of the thieno[3,2-b]thiophene, thieno[3,2-b]furan and 1,2-bis{5-[2-(2-thienyl)ethenyl] 2-thienyl}ethene series

Pavlicic, Davorka,Koruznjak, Jasna Dogan,Banic-Tomisic, Zrinka,Karminski-Zamola, Grace

, p. 871 - 884 (2002)

Three new heterocyclic substituted dianilides, namely 3-chloro-5-[1-(p- fluorophenylcarbamoyl)-2-(2-thienyl)ethenyl]thieno-[3,2-b]thiophene-2-carboxy-p- fluoroanilide (8), 1,2-bis{5-[2-(p-fluorophenylcarbamoyl)-2-(2-thienyl)ethenyl]- 2-thienyl}ethene (13) and 6-chloro-2-{2-[3-chloro-2-(p-fluorophenyl-carbamoyl)- 5-thieno[3,2-b]thienyl]-2-ethoxycarbonylethenyl}thieno[3,2-b] furan-5-carboxy-p-fluoroanilide (20) were prepared by multistep synthesis. The prepared dianilides are of particular interest for their potential to serve as the planar heteroaromatic core of DNA intercalators or groove binders.

New amidino-benzimidazolyl thiophenes: Synthesis and photochemical synthesis

Starcevic, Kristina,Boykin, David W.,Karminski-Zamola, Grace

, p. 218 - 222 (2007/10/03)

The photochemical synthesis of amidino-benzimidazolyl thiophenes was discussed. The amidino-benzimidazolyl-substituted bis-1,2-(2-thienyl) ethenes and benzo[1,2-b:4,3-b′] dithiophenes were prepared by the condensation of amidino-substituted o-phenylene diamines with corresponding dialdehydes. The synthesized bis-cationic bis-amidino benzimidazolyl substituted diphenylfurans were found to inhibit HIV-1 infection.

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