Category: 4412-91-3

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature. 4412-91-3, Name is 3-Furanmethanol, SMILES is OCC1=COC=C1, in an article , author is Ao, Huiting, once mentioned of 4412-91-3, SDS of cas: 4412-91-3.

A new benzofuran glycoside from the fruit ofClausena lansium

In this work, we isolated a new benzofuran glycoside, 6-beta-d-glucosyl-6,7-dihydroxy-5-benzofuranpropanoic acid methyl ester (1), together with six known compounds (2-7) from the fruits ofClausena lansium(Lour.) Skeels. Extensive spectroscopic methods were employed to elucidate their structures. Herein, compounds2,3,5and6were reported fromClausena lansium(Lour.) Skeels for the first time. Moreover, compounds1,2,4and6showed comparable 2,2′-azino-bis(3-ethylbenzthiazoline-6-sulphonic acid) (ABTS) radical scavenging activity tol-ascorbic acid, and compound4also exhibited potent 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical scavenging activity and ferric reducing antioxidant power (FRAP). All of the compounds showed oxygen radical absorbance capacity (ORAC) values ranging from 0.3 to 3.6 mu mol trolex equivalent/mu mol. In addition, compounds3and5also demonstrated good alpha-amylase inhibitory activity.

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Reference:
Benzofuran – Wikipedia,
,Benzofuran | C8H6O – PubChem

Application of 4412-91-3, As an important bridge between the micro and macro material world, chemistry is one of the main methods and means for humans to understand and transform the material world. 4412-91-3, Name is 3-Furanmethanol, SMILES is OCC1=COC=C1, belongs to benzofurans compound. In a article, author is Li, Diyuan, introduce new discover of the category.

Application of Electrochemical Processes to Classical Iodocyclisation: Utility for Selectivity and Mechanistic Insight

The hazards and difficulties of handling elemental halogens such as I-2 can be circumvented through the electrochemical generation of these species in situ and ‘on-demand’. Advantages of this approach include the halogen being introduced into the reaction mixture at a steady rate, ensuring low concentrations to prevent halogenation of reactive aromatic rings. We also demonstrate that the Lewis acid required to promote this reaction, a Zn(II) salt, can also be generated in situ from a zinc-coated graphite electrode in a clean and energy-efficient manner. Mechanistic studies indicate an unusual pathway, which provides selectivity for the iodocyclisation without the often-problematic electrophilic aromatic iodination of the aryl ring.

Application of 4412-91-3, One of the oldest and most widely used commercial enzyme inhibitors is aspirin, which selectively inhibits one of the enzymes involved in the synthesis of molecules that trigger inflammation. you can also check out more blogs about 4412-91-3.

Reference:
Benzofuran – Wikipedia,
,Benzofuran | C8H6O – PubChem