Category: 261767-10-6

The transformation of simple hydrocarbons into more complex and valuable products has revolutionised modern synthetic chemistry. This type of reactivity has quickly become one of the cornerstones of modern catalysis.name: Ethyl 2,3-dihydrobenzo[b][1,4]dioxine-5-carboxylate, In a article, mentioned the application of 261767-10-6, molecular formula is C11H12O4

Containing 1, 4 – benzodioxane of benzene and 1, 2, 4 – triazole class derivative and its preparation and its antibacterial activity (by machine translation)

A containing 1, 4 – benzodioxane of benzene and 1, 2, 4 – triazole class derivatives, has the following general formula: In the formula R is: The invention containing 1, 4 – benzodioxane of benzene and 1, 2, 4 – triazole class derivatives to the bacillus subtilis (B. subtilis), Staphylococcus aureus (S. aureus), Escherichia coli (E.coli), Pseudomonas aeruginosa (P. aeruginosa) is markedly inhibited, so this invention containing 1, 4 – benzodioxane of 1, 2, 4 – triazole class derivatives can be in preparing antibacterial drug application. The invention discloses the preparation method. (by machine translation)

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.name: Ethyl 2,3-dihydrobenzo[b][1,4]dioxine-5-carboxylate, you can also check out more blogs about261767-10-6

Reference：
Benzodioxan,
1,4-Benzodioxane | C8H8O2 – PubChem

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. Quality Control of Ethyl 2,3-dihydrobenzo[b][1,4]dioxine-5-carboxylate, In a article, mentioned the application of 261767-10-6, Name is Ethyl 2,3-dihydrobenzo[b][1,4]dioxine-5-carboxylate, molecular formula is C11H12O4

Benzofuran derivatives, their preparation and use

The present invention relates to benzofuran derivatives having general Formula (I) 1wherein A is selected from (1), (2), (3), (4) 2wherein Z is O or S; s is 0 or 1; q is 0 or 1; R4 is hydrogen, C1-6-alkyl, C2-6-alkenyl, C26-alkynyl, C1-6-alkyl-aryl, or C1-6-alkyl-O-aryl; D is a spacer group selected from branched or straight chain C1-6-alkylene, C2-6-alkenylene and C2-6-alkynylene; its enantiomers, and pharmaceutically acceptable acid addition salt thereof. The compounds are potently binding to the 5-HT1A receptor.

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Reference：
Benzodioxan,
1,4-Benzodioxane | C8H8O2 – PubChem

Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments. Quality Control of Ethyl 2,3-dihydrobenzo[b][1,4]dioxine-5-carboxylate. Introducing a new discovery about 261767-10-6, Name is Ethyl 2,3-dihydrobenzo[b][1,4]dioxine-5-carboxylate

Containing 1, 4 – benzodioxane of benzene and 1, 2, 4 – triazole class derivative and its preparation and its antibacterial activity (by machine translation)

A containing 1, 4 – benzodioxane of benzene and 1, 2, 4 – triazole class derivatives, has the following general formula: In the formula R is: The invention containing 1, 4 – benzodioxane of benzene and 1, 2, 4 – triazole class derivatives to the bacillus subtilis (B. subtilis), Staphylococcus aureus (S. aureus), Escherichia coli (E.coli), Pseudomonas aeruginosa (P. aeruginosa) is markedly inhibited, so this invention containing 1, 4 – benzodioxane of 1, 2, 4 – triazole class derivatives can be in preparing antibacterial drug application. The invention discloses the preparation method. (by machine translation)

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Quality Control of Ethyl 2,3-dihydrobenzo[b][1,4]dioxine-5-carboxylate, you can also check out more blogs about261767-10-6

Reference£º
Benzodioxan,
1,4-Benzodioxane | C8H8O2 – PubChem

Chemistry is traditionally divided into organic and inorganic chemistry. Quality Control of Ethyl 2,3-dihydrobenzo[b][1,4]dioxine-5-carboxylate, The former is the study of compounds containing at least one carbon-hydrogen bonds.In a patent£¬Which mentioned a new discovery about 261767-10-6

Benzofuran derivatives, their preparation and use

The present invention relates to benzofuran derivatives having general Formula (I) 1wherein A is selected from (1), (2), (3), (4) 2wherein Z is O or S; s is 0 or 1; q is 0 or 1; R4 is hydrogen, C1-6-alkyl, C2-6-alkenyl, C26-alkynyl, C1-6-alkyl-aryl, or C1-6-alkyl-O-aryl; D is a spacer group selected from branched or straight chain C1-6-alkylene, C2-6-alkenylene and C2-6-alkynylene; its enantiomers, and pharmaceutically acceptable acid addition salt thereof. The compounds are potently binding to the 5-HT1A receptor.

If you are interested in 261767-10-6, you can contact me at any time and look forward to more communication. Quality Control of Ethyl 2,3-dihydrobenzo[b][1,4]dioxine-5-carboxylate

Reference£º
Benzodioxan,
1,4-Benzodioxane | C8H8O2 – PubChem

Synthetic Route of 261767-10-6, A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 261767-10-6, Name is Ethyl 2,3-dihydrobenzo[b][1,4]dioxine-5-carboxylate, molecular formula is C11H12O4. In a Article£¬once mentioned of 261767-10-6

Synthesis and antibacterial activity of cinnamaldehyde acylhydrazone with a 1,4-benzodioxan fragment as a novel class of potent ss-Ketoacyl-acyl carrier protein synthase III (FabH) inhibitor

Fatty acid biosynthesis is essential for bacterial survival. ss-Ketoacyl-acyl carrier protein (ACP) synthase III (FabH), is a particularly attractive antibacterial target, since it is central to the initiation of fatty acid biosynthesis. Three series of 21 cinnamaldehyde acylhydrazone derivatives, A3-9, B3-9, and C3-9, were synthesized and evaluated for FabH-inhibitory activity. Compound B6 showed the most potent biological activity against Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus, and Bacillus subtilis (minimum inhibitory concentrations (MICs) values: 1.56-3.13mug/mL) and was comparable with the positive control. Docking simulation by positioning compound B6 in the FabH structure active site was performed to explore the possible binding model.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Synthetic Route of 261767-10-6. In my other articles, you can also check out more blogs about 261767-10-6

Reference£º
Benzodioxan,
1,4-Benzodioxane | C8H8O2 – PubChem

Reference of 261767-10-6, Chemistry is the science of change. But why do chemical reactions take place? Why do chemicals react with each other? The answer is in thermodynamics and kinetics.In a document type is Patent, and a compound is mentioned, 261767-10-6, Ethyl 2,3-dihydrobenzo[b][1,4]dioxine-5-carboxylate, introducing its new discovery.

DIHYDROBENZODIOXINE CARBOXAMIDE AND KETONE DERIVATIVES

This invention relates to certain 5-HT 4 receptor modulators, particularly 5-HT 4 receptor antagonists, represented by Formula I: wherein Z is formula (A) or (B): wherein R 1, R 2, R 3, R 4, and R 5 and the other substituents are as defined in the specification; or individual isomers, racemic or non-racemic mixtures of isomers, and pharmaceutically acceptable salts or solvates thereof. The invention further relates to pharmaceutical compositions containing such compounds and methods for their use as therapeutic agents.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Reference of 261767-10-6. In my other articles, you can also check out more blogs about 261767-10-6

Reference£º
Benzodioxan,
1,4-Benzodioxane | C8H8O2 – PubChem

Name is Ethyl 2,3-dihydrobenzo[b][1,4]dioxine-5-carboxylate, as a common heterocyclic compound, it belongs to benzodioxans compound, and cas is 261767-10-6, its synthesis route is as follows.

Example 5 5-hydroxymethyl-1,4-benzodioxan (5). To a suspension of lithium aluminum hydride (7.0 g, 0.18 mmol) in dry diethyl ether (100 mL) was added a solution of ethyl 1,4-benzodioxan-5-carboxylate (35 g, 0.17 mmol) in diethyl ether (100 mL). After boiling under reflux for 2 h, the reaction mixture was cooled to 0 C. and carefully treated with water (35 mL) and 4N aqueous sodium hydroxide (35 mL). The resulting mixture was filtered and dried (Na2SO4). Evaporation of the solvents afforded 25 g (88%) crystalline title compound: mp 51-53 C.; 1H NMR (CDCl3) delta 2.50 (s, 1H), 4.20-4.3 (m, 4H), 4.60 (s, 2H), 6.75-6.90 (m, 3H).

261767-10-6, In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles.,261767-10-6 ,Ethyl 2,3-dihydrobenzo[b][1,4]dioxine-5-carboxylate, other downstream synthetic routes, hurry up and to see

Reference£º
Patent; H. Lundbeck A/S; US2002/32205; (2002); A1;,
Benzodioxan
1,4-Benzodioxane | C8H8O2 – PubChem

As a common heterocyclic compound, it belongs to quinuclidine compound,Quinuclidine-4-carboxylic acid hydrochloride,40117-63-3,Molecular formula: C8H14ClNO140,mainly used in chemical industry, its synthesis route is as follows.,261767-10-6

Example 5 5-hydroxymethyl-1,4-benzodioxan (5). To a suspension of lithium aluminum hydride (7.0 g, 0.18 mmol) in dry diethyl ether (100 mL) was added a solution of ethyl 1,4-benzodioxan-5-carboxylate (35 g, 0.17 mmol) in diethyl ether (100 mL). After boiling under reflux for 2 h, the reaction mixture was cooled to 0 C. and carefully treated with water (35 mL) and 4N aqueous sodium hydroxide (35 mL). The resulting mixture was filtered and dried (Na2SO4). Evaporation of the solvents afforded 25 g (88%) crystalline title compound: mp 51-53 C.; 1H NMR (CDCl3) delta 2.50 (s, 1H), 4.20-4.3 (m, 4H), 4.60 (s, 2H), 6.75-6.90 (m, 3H).

With the complex challenges of chemical substances, we look forward to future research findings about Ethyl 2,3-dihydrobenzo[b][1,4]dioxine-5-carboxylate,belong benzodioxans compound

Reference£º
Patent; H. Lundbeck A/S; US2002/32205; (2002); A1;,
Benzodioxan
1,4-Benzodioxane | C8H8O2 – PubChem

261767-10-6, Ethyl 2,3-dihydrobenzo[b][1,4]dioxine-5-carboxylate is a benzodioxans compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated,261767-10-6

Example 5 5-hydroxymethyl-1,4-benzodioxan (5). To a suspension of lithium aluminum hydride (7.0 g, 0.18 mmol) in dry diethyl ether (100 mL) was added a solution of ethyl 1,4-benzodioxan-5-carboxylate (35 g, 0.17 mmol) in diethyl ether (100 mL). After boiling under reflux for 2 h, the reaction mixture was cooled to 0 C. and carefully treated with water (35 mL) and 4N aqueous sodium hydroxide (35 mL). The resulting mixture was filtered and dried (Na2SO4). Evaporation of the solvents afforded 25 g (88%) crystalline title compound: mp 51-53 C.; 1H NMR (CDCl3) delta 2.50 (s, 1H), 4.20-4.3 (m, 4H), 4.60 (s, 2H), 6.75-6.90 (m, 3H).

As the paragraph descriping shows that 261767-10-6 is playing an increasingly important role.

Reference£º
Patent; H. Lundbeck A/S; US2002/32205; (2002); A1;,
Benzodioxan
1,4-Benzodioxane | C8H8O2 – PubChem