57329-40-5 Usage
Description
(2E)-3-(1-Benzofuran-2-yl)acrylic acid is a chemical compound with a molecular formula C12H8O3. It is a derivative of acrylic acid with a benzofuran ring attached to the carbon-carbon double bond. This yellow solid with a strong odor is commonly used in the synthesis of organic compounds and pharmaceuticals due to its unique structure and reactivity. Additionally, it has potential applications in the field of materials science and organic electronics. Its specific properties and potential uses make it a valuable compound in various scientific and industrial applications.
Uses
Used in Pharmaceutical Industry:
(2E)-3-(1-Benzofuran-2-yl)acrylic acid is used as a key intermediate in the synthesis of pharmaceuticals for its unique structure and reactivity, contributing to the development of new drugs with potential therapeutic benefits.
Used in Organic Synthesis:
(2E)-3-(1-Benzofuran-2-yl)acrylic acid is used as a building block in organic synthesis for creating a variety of complex organic compounds, leveraging its reactive properties to form new chemical entities.
Used in Materials Science:
(2E)-3-(1-Benzofuran-2-yl)acrylic acid is used as a component in the development of advanced materials, taking advantage of its structural features to enhance material properties for specific applications.
Used in Organic Electronics:
(2E)-3-(1-Benzofuran-2-yl)acrylic acid is used in the field of organic electronics for its potential to contribute to the creation of novel electronic devices and components, such as organic light-emitting diodes (OLEDs) and organic solar cells, due to its electronic properties.
Check Digit Verification of cas no
The CAS Registry Mumber 57329-40-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,3,2 and 9 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 57329-40:
(7*5)+(6*7)+(5*3)+(4*2)+(3*9)+(2*4)+(1*0)=135
135 % 10 = 5
So 57329-40-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H8O3/c12-11(13)6-5-9-7-8-3-1-2-4-10(8)14-9/h1-7H,(H,12,13)/b6-5+
57329-40-5Relevant articles and documents
Photocatalytic decarboxylative alkenylation of α-amino and α-hydroxy acid-derived redox active esters by NaI/PPh3 catalysis
Fu, Ming-Chen,Fu, Yao,Shang, Rui,Wang, Ya-Ting,Zhao, Bin
supporting information, p. 2495 - 2498 (2020/03/06)
Herein, we report the photocatalytic decarboxylative alkenylation reactions of N-(acyloxy)phthalimide derived from α-amino and α-hydroxy acids with 1,1-diarylethene, and with cinnamic acid derivatives through double decarboxylation, using sodium iodide and triphenylphosphine as redox catalysts. The reaction proceeds under mild irradiation conditions with visible blue light (440 nm or 456 nm) in an acetone solvent without recourse to transition-metal or organic dye based photoredox catalysts. The reaction proceeds via photoactivation of a transiently self-assembled chromophore from N-(acyloxy)phthalimide and NaI/PPh3. Solvation plays a crucial role in the reactivity.
PROTEIN KINASE C AGONISTS
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Paragraph 0281, (2020/09/12)
The present disclosure relates generally to certain diacylglycerol lactone compounds, pharmaceutical compositions comprising said compounds, and methods of making and using said compounds and pharmaceutical compositions. The compounds and compositions dis
Synthesis of 2-amino-4-(2-benzofuryl)Δ1 pyrrolines and study of their antidysrhythmic properties
Maillard,Langlois,Vo Van,et al.
, p. 353 - 358 (2007/10/02)
The synthesis of 2-amino 4(2-benzofuryl)Δ1 pyrrolines, substituted in the aromatic ring and/or on the nitrogen atom of the amino group, is described. These derivatives are obtained from 3 (2-benzofuryl) acrylic esters, on which nitromethane is added. The reduction of 4-nitrobutyric esters lead to pyrrolidinones, and then to the entitled derivatives. Some analogs, the benzofuran ring of which is replaced by another heterocycle, were also prepared. Some of them exhibit interesting antidysrhythmic properties.
