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2-(2,4-dimethylphenyl)benzofuran is an organic compound characterized by a benzofuran ring system, which consists of a benzene ring fused to a furan ring. The molecule features a 2,4-dimethylphenyl group attached to the benzofuran core, where the methyl groups are located at the 2nd and 4th carbon positions of the phenyl ring. This chemical structure contributes to its unique properties and potential applications in various fields, such as pharmaceuticals, agrochemicals, or materials science. The compound's specific molecular formula is C15H14O, and it has a molecular weight of 206.27 g/mol. Its chemical structure and properties make it an interesting target for synthesis and investigation in the realm of organic chemistry.

19290-26-7

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19290-26-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19290-26-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,2,9 and 0 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 19290-26:
(7*1)+(6*9)+(5*2)+(4*9)+(3*0)+(2*2)+(1*6)=117
117 % 10 = 7
So 19290-26-7 is a valid CAS Registry Number.

19290-26-7Downstream Products

19290-26-7Relevant academic research and scientific papers

Copper-promoted hydration and annulation of 2-fluorophenylacetylene derivatives: From alkynes to benzo[b]furans and benzo[b]thiophenes

Li, Yibiao,Cheng, Liang,Liu, Xiaohang,Li, Bin,Sun, Ning

, p. 2886 - 2891 (2014)

An efficient copper-promoted hydration reaction and its application in the synthesis of benzo[b ] furan and benzo[ b ] thiophene derivatives is presented starting from readily available 2-fluorophenylacetylene derivatives. The key annulation step involves

Acid-mediated intermolecular C-F/C-H cross-coupling of 2-fluorobenzofurans with arenes: Synthesis of 2-arylbenzofurans

Fujita, Takeshi,Morioka, Ryutaro,Fukuda, Takuya,Suzuki, Naoto,Ichikawa, Junji

supporting information, p. 8500 - 8503 (2021/08/31)

Transition-metal-free acid-promoted biaryl construction was achieved via intermolecular C-F/C-H cross-coupling. By treating 2-fluorobenzofurans with arenes in the presence of AlCl3, 2-arylbenzofurans were obtained. This protocol was successfully applied to the short-step orthogonal synthesis of a bioactive 2-arylbenzofuran natural product, which allows independent transformations of C-F and C-Br bonds. Mechanistic studies indicated that α-fluorine-stabilized carbocations, generated via the protonation of 2-fluorobenzofurans, served as key intermediates. The Friedel-Crafts-type C-C bond formation between the α-fluorocarbocations and arenes, followed by hydrogen fluoride elimination, afforded 2-arylbenzofurans. This journal is

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