58491-51-3

Upstream product

• 1548158-01-5 C₁₇H₁₆O₃ 
• 1620885-66-6 C₁₆H₁₂Br₂O 
• 25664-48-6 2-p-tolyl-benzofuran 
• 68-12-2 N,N-dimethyl-formamide 
• 104-82-5 4-Methylbenzyl chloride 
• 1530-37-6 (4-methylbenzyl)triphenylphosphonium chloride 
• 58358-48-8 Ε-2-(4-methylstyryl)phenol 
• 90-02-8 salicylaldehyde 

Downstream Products

• 58491-52-4 2-(4-methylphenyl)benzofuran-3-carboxylic acid 

Relevant academic research and scientific papers

Preparation and application of 2-(4-substituted phenyl)-3-formamide benzofuranene cyanide compound

The invention provides a preparation and application of a 2-(4-substituted phenyl)-3-formamide benzofuranene cyanide compound. The benzofuranene cyanide compound shown in formula I has a structure shown in the following formula I, wherein the definition o

Synthesis, biological evaluation and molecular docking analysis of 2-phenyl-benzofuran-3-carboxamide derivatives as potential inhibitors of Staphylococcus aureus Sortase A

In Gram-positive bacteria, Sortase A (Srt A) is a critical cysteine transpeptidase that is responsible for recognizing and assembling surface virulence proteins through the recognition of a LPXTG (leucine, proline, X, threonine, and glycine, where X is an

Benzofuran compound, preparation method and applications thereof

The present invention provides a benzofuran compound, a preparation method and applications thereof, wherein the structure is represented by a general formula (I-1) or (I-2), R1, R3 and R4 are any one selected from hydrogen, C1-C5 straight or branched cha

Benzofuran compounds intermediates, and preparation method and application thereof

The invention provides a kind of benzofuran compounds intermediates, and a preparation method and application thereof, and the structure of the intermediates is shown as a general formula (I) in the specification. In the general formula (I), R1 and R3 are

A novel efficient protocol for preparation of 3-formyl-2-arylbenzo[b]furan derivatives

An efficient method for preparation of 3-formyl-2-arylbenzo[b]furan derivatives 4 from 3-chloro-2-(2-methoxyaryl)-1-arylprop-2-en-1-one 2 was developed, and the desired product was obtained in good to excellent yields. By converting 2-(2-methoxyphenyl)-3-oxo-3-phenylpropanal 1 to 2, the regioselectivity problem occurring in the reaction when using 1 as the starting material was successfully avoided. Furthermore, a one-pot procedure for the successive demethylation, cyclization, and hydrolysis was evolved, although the intermediate 3-(dibromomethyl)-2-phenylbenzo[b]furan 3a could be isolated. A plausible mechanism was proposed based on some in situ investigations.