Category: 13196-10-6

Use of compounds in conjunction with fertilizers was written by Anonymous. And the article was included in Research Disclosure in 1975.Electric Literature of C8H6O2 This article mentions the following:

Compounds of the formula I (where R1 to R4 may be the same or different alkyl groups) are used in conjunction with fast or slow acting fertilizers to retard plant growth. Thus, I (R1 = R2 = R4 = Me; R3 = Et [26225-79-6]) was applied either at the same time or 3-4 weeks subsequent to the application of solid or liquid form fertilizers. When applied as a mixture with a slow-release fertilizer the preferred proportion was 15-60 parts by weight of N and 1-4 parts I. In the experiment, the researchers used many compounds, for example, Benzofuran-5-ol (cas: 13196-10-6Electric Literature of C8H6O2).

Benzofuran-5-ol (cas: 13196-10-6) belongs to benzofurans derivatives. Benzofuran is a core structural unit found in many naturally occurring compounds with multidirectional biological activities. As benzofurans are prone to undergo ring opening of the heterocycle, examples of reduction of this type of aromatics by using dissolving metals are rather scarce.Electric Literature of C8H6O2

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

A theoretical study of 2-nitrofuran vs 3-nitrofuran as dienophilic electrophile in polar cycloaddition reaction: comparison of the reactivity and reaction mechanism was written by Cainelli, Mauro;Ormachea, Carla M.;Mancini, Pedro M. E.;Kneeteman, Maria N.. And the article was included in International Research Journal of Pure and Applied Chemistry in 2016.Name: Benzofuran-5-ol This article mentions the following:

In this study, we analyzed in a theor. form the behavior of 2-nitrofuran and 3-nitrofuran acting as dienophilic electrophiles in polar cycloaddition reactions joint to different dienes. The reactivity and regioselectivity was discussed employing global and local reactivity indexes, resp. The reaction mechanisms of these cycloadditions were compared through the transition state structures and energies calculated In the experiment, the researchers used many compounds, for example, Benzofuran-5-ol (cas: 13196-10-6Name: Benzofuran-5-ol).

Benzofuran-5-ol (cas: 13196-10-6) belongs to benzofurans derivatives. Benzofurans are only weakly aromatic in nature and they are cleaved by many oxidative and reductive conditions. Benzofurans are stable towards alkali and readily polymerize on treatment with sulfuric acid, due to which they are useful for the preparation of low cost chemically relatively inert resins.Name: Benzofuran-5-ol

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Polymer-supported eosin Y as a reusable photocatalyst for visible light mediated organic transformations was written by Sridhar, Arunasalam;Rangasamy, Rajmohan;Selvaraj, Mari. And the article was included in New Journal of Chemistry in 2019.HPLC of Formula: 13196-10-6 This article mentions the following:

A novel polymer-supported recyclable photocatalyst was developed for visible light mediated oxidation reactions. The organic dye eosin Y was loaded on macroporous com. available Amberlite IRA 900 chloride resin and exploited as a photocatalyst for visible light mediated oxidation of thioethers to sulfoxides and phenylboronic acids to phenols under open atm. air. Varieties of functional groups were well tolerated during oxidation The catalyst is recyclable for six cycles without significant loss in its efficiency. Furthermore, gram-scale oxidation of sulfides to sulfoxides was demonstrated to prove the com. viability of the method. In the experiment, the researchers used many compounds, for example, Benzofuran-5-ol (cas: 13196-10-6HPLC of Formula: 13196-10-6).

Benzofuran-5-ol (cas: 13196-10-6) belongs to benzofurans derivatives. Benzofuran is a core structural unit found in many naturally occurring compounds with multidirectional biological activities. In nature, benzofurans have occupied an important role among the plant phenols & several pharmacologically active compounds.HPLC of Formula: 13196-10-6

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Pd-Catalyzed Synthesis of Aryl and Heteroaryl Triflones from Reactions of Sodium Triflinate with Aryl (Heteroaryl) Triflates was written by Smyth, Lynette A.;Phillips, Eric M.;Chan, Vincent S.;Napolitano, Jose G.;Henry, Rodger;Shekhar, Shashank. And the article was included in Journal of Organic Chemistry in 2016.Application In Synthesis of Benzofuran-5-ol This article mentions the following:

A novel method for Pd-catalyzed triflination of aryl and heteroaryl triflates using NaSO₂CF₃ as the nucleophile is described. The combination of Pd₂(dba)₃ and RockPhos formed the most effective catalyst. A broad range of functional groups and heteroaromatic compounds were tolerated under the neutral reaction conditions. The order of reactivity ArOTf ≥ ArCl ≥ ArBr is consistent with transmetalation being a slow step of the reaction. In the experiment, the researchers used many compounds, for example, Benzofuran-5-ol (cas: 13196-10-6Application In Synthesis of Benzofuran-5-ol).

Benzofuran-5-ol (cas: 13196-10-6) belongs to benzofurans derivatives. Benzofuran is the “”parent”” of many related compounds with more complex structures. For example, psoralen is a benzofuran derivative that occurs in several plants. Benzofurans have also made significant and distinctive contributions to biology. They exhibit several biological activities that range from antioxidant, antitubercular, antiplasmodial, insecticidal.Application In Synthesis of Benzofuran-5-ol

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Benzofuran Derivatives as Potent, Orally Active S1P1 Receptor Agonists: A Preclinical Lead Molecule for MS was written by Saha, Ashis K.;Yu, Xiang;Lin, Jian;Lobera, Mercedes;Sharadendu, Anurag;Chereku, Srinivas;Schutz, Nili;Segal, Dalia;Marantz, Yael;McCauley, Dilara;Middleton, Scot;Siu, Jerry;Burli, Roland W.;Buys, Janet;Horner, Michelle;Salyers, Kevin;Schrag, Michael;Vargas, Hugo M.;Xu, Yang;McElvain, Michele;Xu, Han. And the article was included in ACS Medicinal Chemistry Letters in 2011.Formula: C8H6O2 This article mentions the following:

Novel benzofuran-based S1P₁ agonists with excellent in vitro potency and selectivity were prepared 1-{[4-(5-Benzylbenzofuran-2-yl)-3-fluorophenyl]methyl}azetidine-3-carboxylic acid is a potent S1P₁ agonist with >1000× selectivity over S1P₃. It demonstrated a good in vitro ADME profile and excellent oral bioavailability across species. Dosed orally at 0.3 mg/kg, I significantly reduced blood lymphocyte counts 24 h postdose and demonstrated efficacy in a mouse EAE model of relapsing MS. In the experiment, the researchers used many compounds, for example, Benzofuran-5-ol (cas: 13196-10-6Formula: C8H6O2).

Benzofuran-5-ol (cas: 13196-10-6) belongs to benzofurans derivatives. Many natural or synthetic compounds containing benzofuran skeletons have been found to possess remarkable activity as agrochemicals and pharmaceuticals. In nature, benzofurans have occupied an important role among the plant phenols & several pharmacologically active compounds.Formula: C8H6O2

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Benzofuran Derivatives as Potent, Orally Active S1P1 Receptor Agonists: A Preclinical Lead Molecule for MS was written by Saha, Ashis K.;Yu, Xiang;Lin, Jian;Lobera, Mercedes;Sharadendu, Anurag;Chereku, Srinivas;Schutz, Nili;Segal, Dalia;Marantz, Yael;McCauley, Dilara;Middleton, Scot;Siu, Jerry;Burli, Roland W.;Buys, Janet;Horner, Michelle;Salyers, Kevin;Schrag, Michael;Vargas, Hugo M.;Xu, Yang;McElvain, Michele;Xu, Han. And the article was included in ACS Medicinal Chemistry Letters in 2011.Formula: C8H6O2 This article mentions the following:

Novel benzofuran-based S1P₁ agonists with excellent in vitro potency and selectivity were prepared 1-{[4-(5-Benzylbenzofuran-2-yl)-3-fluorophenyl]methyl}azetidine-3-carboxylic acid is a potent S1P₁ agonist with >1000× selectivity over S1P₃. It demonstrated a good in vitro ADME profile and excellent oral bioavailability across species. Dosed orally at 0.3 mg/kg, I significantly reduced blood lymphocyte counts 24 h postdose and demonstrated efficacy in a mouse EAE model of relapsing MS. In the experiment, the researchers used many compounds, for example, Benzofuran-5-ol (cas: 13196-10-6Formula: C8H6O2).

Benzofuran-5-ol (cas: 13196-10-6) belongs to benzofurans derivatives. Many natural or synthetic compounds containing benzofuran skeletons have been found to possess remarkable activity as agrochemicals and pharmaceuticals. In nature, benzofurans have occupied an important role among the plant phenols & several pharmacologically active compounds.Formula: C8H6O2

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem