Category: 886361-30-4

886361-30-4, Name is Methyl 2-amino-5-(4-fluorophenyl)thiazole-4-carboxylate, molecular formula is C11H9FN2O2S, belongs to thiazole compound, is a common compound. In a patnet, once mentioned the new application about 886361-30-4, Computed Properties of C11H9FN2O2S

The invention relates to novel 2-aza-bicyclo[2.2.1]heptane derivatives of formula (I), wherein A, B, n and R1 are as described in the description, and to the use of such compounds, or of pharmaceutically acceptable salts of such compounds, as medicaments, especially as orexin receptor antagonists.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.category: thiazole. In my other articles, you can also check out more blogs about 886361-30-4

Reference：
Thiazole | C3H8409NS – PubChem,
Thiazole | chemical compound | Britannica

Children learn through play, and they learn more than adults might expect. Science experiments are a great way to spark their curiosity, get their minds active, and encourage them to do something that doesn’t involve a screen. 886361-30-4, C11H9FN2O2S. A document type is Patent, introducing its new discovery., name: Methyl 2-amino-5-(4-fluorophenyl)thiazole-4-carboxylate

The invention relates to thiazolidine derivatives of the formula (I) wherein A, B, and R1 are as described in the description, to salts, especially pharmaceutically acceptable salts, of such compounds and to their use as medicaments, especially as orexin receptor antagonists.

Interested yet? Keep reading other articles of 886361-30-4!, name: Methyl 2-amino-5-(4-fluorophenyl)thiazole-4-carboxylate

Reference：
Thiazole | C3H8404NS – PubChem,
Thiazole | chemical compound | Britannica

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. 886361-30-4, Name is Methyl 2-amino-5-(4-fluorophenyl)thiazole-4-carboxylate, molecular formula is C11H9FN2O2S. In a Patent，once mentioned of 886361-30-4, Recommanded Product: 886361-30-4

The invention relates to thiazolidine derivatives of the formula (I) wherein A, B, and R1 are as described in the description, to salts, especially pharmaceutically acceptable salts, of such compounds and to their use as medicaments, especially as orexin receptor antagonists

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Recommanded Product: 886361-30-4. In my other articles, you can also check out more blogs about 886361-30-4

Reference：
Thiazole | C3H8405NS – PubChem,
Thiazole | chemical compound | Britannica

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. 886361-30-4, Name is Methyl 2-amino-5-(4-fluorophenyl)thiazole-4-carboxylate, molecular formula is C11H9FN2O2S. In a Patent，once mentioned of 886361-30-4, HPLC of Formula: C11H9FN2O2S

The invention relates to 3-aza-bicyclo[3.3.0]octane derivatives of the formula (I) wherein R1, R2, R3, and A are as described in the description and their use as orexin receptor antagonists.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.HPLC of Formula: C11H9FN2O2S. In my other articles, you can also check out more blogs about 886361-30-4

Reference：
Thiazole | C3H8411NS – PubChem,
Thiazole | chemical compound | Britannica

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.886361-30-4, Name is Methyl 2-amino-5-(4-fluorophenyl)thiazole-4-carboxylate, molecular formula is C11H9FN2O2S. In a Patent£¬once mentioned of 886361-30-4, name: Methyl 2-amino-5-(4-fluorophenyl)thiazole-4-carboxylate

The invention relates to 2-aza-bicyclo[3.3.0]octane deriva- tives of Formula (I) whereinA, B, and R1 are as described in the description, and to the use of such compounds, or of pharmaceutically acceptable salts of such compounds, as medicaments, especially as orexin receptor antagonists.

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: Methyl 2-amino-5-(4-fluorophenyl)thiazole-4-carboxylate, you can also check out more blogs about886361-30-4

Reference£º
Thiazole | C3H8413NS – PubChem,
Thiazole | chemical compound | Britannica

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. 886361-30-4, Name is Methyl 2-amino-5-(4-fluorophenyl)thiazole-4-carboxylate, molecular formula is C11H9FN2O2S. In a Patent£¬once mentioned of 886361-30-4, Formula: C11H9FN2O2S

The invention relates to oxazolidine derivatives of the formula (I) wherein A, B, and R 1 are as described in the description, to salts, especially pharmaceutically acceptable salts, of such compounds and to their use as medicaments, especially as orexin receptor antagonists

The invention relates to oxazolidine derivatives of the formula (I) wherein A, B, and R 1 are as described in the description, to salts, especially pharmaceutically acceptable salts, of such compounds and to their use as medicaments, especially as orexin receptor antagonists

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Formula: C11H9FN2O2S. In my other articles, you can also check out more blogs about 886361-30-4

Reference£º
Thiazole | C3H8408NS – PubChem,
Thiazole | chemical compound | Britannica

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.886361-30-4,Methyl 2-amino-5-(4-fluorophenyl)thiazole-4-carboxylate,as a common compound, the synthetic route is as follows.

To a solution of P-29 (1g, 3.96mmol) in pyridine (10 mL) was added methanesulfonyl chloride (0.62mL, 7.92mmol) and the resulting mixture was stuffed at 60C over night. Reaction mixture was then brought to room temperature and pyridine was evaporated under reduced pressure. The residue was dissolved in ethyl acetate and washed with saturated aq. sodium bicarbonate, water and brine. Organic layer was dried with anhydrous sodium sulfate, filtered and concentrated. The residue was purified by flash chromatography (hexanes/ethyl acetate) to afford 1g (77%) of product 12. To a stuffed suspension of intermediate 2 (1g, 3mmol) was added 2M LiOH in dioxane (7.5mL, 3mmol) and the solution was stirred for 2h at 40C. The reaction mixture was then gradually acidified with 1N HCl. Diluted with water and extracted with ethyl acetate. Organic layer was washed with brine and dried with anhydrous sodium sulfate. Filtration and evaporation of organic layer afforded 0.9g (94%) of the product S-29., 886361-30-4

886361-30-4 Methyl 2-amino-5-(4-fluorophenyl)thiazole-4-carboxylate 2782963, athiazole compound, is more and more widely used in various fields.

Reference£º
Patent; FLYNN, Gary, A.; WO2013/22766; (2013); A1;,
Thiazole | C3H3NS – PubChem
Thiazole | chemical compound | Britannica

886361-30-4, Methyl 2-amino-5-(4-fluorophenyl)thiazole-4-carboxylate is a thiazole compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

In an inert atmosphere, copper(II)bromide (47.3 mmol, 1.0 eq) was suspended in MeCN (200 mL) and cooled to 5-10 C. followed by the addition of 3-methylbutylnitrite (71 mmol, 1.45 eq) over 15 min. To this reaction mixture the respective 2-aminothiazole derivative (47.3 mmol, 1 eq) was added in portions over 35 min at 5-10 C. The reaction mixture was then carefully heated to 65 C. and stirring continued for 2 h. The volatiles were removed under reduced pressure and the black residue was purified by FC (heptane/EtOAc, as the appropriate mixture) to give the products as slightly yellow oils or solids

886361-30-4, 886361-30-4 Methyl 2-amino-5-(4-fluorophenyl)thiazole-4-carboxylate 2782963, athiazole compound, is more and more widely used in various fields.

Reference£º
Patent; Aissaoui, Hamed; Boss, Christoph; Gude, Markus; Koberstein, Ralf; Sifferlen, Thierry; US2010/222328; (2010); A1;,
Thiazole | C3H3NS – PubChem
Thiazole | chemical compound | Britannica