Category: 884-22-0

Electric Literature of 884-22-0, An article , which mentions 884-22-0, molecular formula is C10H9NO3S. The compound – Methyl 6-methoxybenzo[d]thiazole-2-carboxylate played an important role in people’s production and life.

The invention discloses a method for synthesizing aromatic heterocyclic methyl ester compounds, namely to the molecular formula is [(ArN=C (CH3 ) NCH2 CH2 NCH2 C6 H5 ) CH] of Cl imidazole chlorine salt (wherein Ar=2, 6 – II – CH (CH3 )2 – C6 H3 ) As catalyst, normal pressure through the aromatic heterocyclic compound and carbon dioxide of the carboxylation reaction to synthesize aromatic heterocyclic methyl ester compound. This is by the imidazole salt catalyzed by aromatic heterocyclic compound and carbon dioxide of the carboxylation reaction to prepare aromatic heterocyclic methyl ester compound of the 1st example, compared with the prior art, not only the catalyst more green, synthetic more easily, and the mild reaction conditions, with equal or better tolerability of catalytic activity and functional group. (by machine translation)

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Reference：
Thiazole | C3H8506NS – PubChem,
Thiazole | chemical compound | Britannica

Synthetic Route of 884-22-0, Chemistry can be defined as the study of matter and the changes it undergoes. You’ll sometimes hear it called the central science because it is the connection between physics and all the other sciences, starting with biology.884-22-0, Name is Methyl 6-methoxybenzo[d]thiazole-2-carboxylate, molecular formula is C10H9NO3S. In a patent, introducing its new discovery.

Selective NR1/2B N-methyl-D-aspartate receptor antagonists among indole-2-carboxamides and benzimidazole-2-carboxamides

(4-Benzylpiperidine-1-yl)-(6-hydroxy-1H-indole-2-yl)-methanone (6a) derived from (E)-1 -(4-benzylpiperidin-1-yl)-3-(4-hydroxy-phenyl)-propenone (5) was identified as a potent NR2B subunit-selective antagonist of the NMDA receptor. To establish the structure-activity relationship (SAR) and to attempt the improvement of the ADME properties of the lead, a series of compounds were prepared and tested. Several derivatives showed low nanomolar activity both in the binding and in the functional assay. In a formalin-induced hyperalgesia model in mice, 6a and (4-benzylpiperidine-1-yl)-[5(6)-hydroxy-1H-benzimidazol-2- yl]-methanone (60a) were as active as besonprodil (2) after oral administration. A CoMS1A model was developed based on binding data of a series of indole- and benzimidazole-2-carboxamides.

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Reference：
Thiazole | C3H8511NS – PubChem,
Thiazole | chemical compound | Britannica

In an article, published in an article, once mentioned the application of 884-22-0, Name is Methyl 6-methoxybenzo[d]thiazole-2-carboxylate,molecular formula is C10H9NO3S, is a conventional compound. this article was the specific content is as follows.Computed Properties of C10H9NO3S

Direct C-H carboxylation with carbon dioxide using 1,2,3-triazol-5-ylidene copper(I) complexes

1,2,3-Triazol-5-ylidene copper(I) complexes (tzNHC-Cu) efficiently catalyzed the direct C-H carboxylation of benzoxazole and benzothiazole derivatives with CO2 to give the corresponding esters in excellent yields after treatment with alkyl iodide. The tzNHC copper(I) complex, i.e., [(TPr)CuCl], worked somewhat more effectively than the corresponding imidazol-2-ylidene copper(I) complex [(IPr)CuCl] to give the carboxylation product in higher yields.

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Reference：
Thiazole | C3H8510NS – PubChem,
Thiazole | chemical compound | Britannica

In an article, published in an article, once mentioned the application of 884-22-0, Name is Methyl 6-methoxybenzo[d]thiazole-2-carboxylate,molecular formula is C10H9NO3S, is a conventional compound. this article was the specific content is as follows.HPLC of Formula: C10H9NO3S

A number of benzothiazolylthienothiophenes have been synthesized. Spectral studies have revealed that all these compounds have fluorescent properties that depend on their structure. Dependence of absorption and fluorescence bands positions on the nature of substituents have been established. Increase of the electron-withdrawing nature of substituents led to bathochromic shift of the absorption and fluorescence bands as well as to decrease of the fluorescence intensity.

A number of benzothiazolylthienothiophenes have been synthesized. Spectral studies have revealed that all these compounds have fluorescent properties that depend on their structure. Dependence of absorption and fluorescence bands positions on the nature of substituents have been established. Increase of the electron-withdrawing nature of substituents led to bathochromic shift of the absorption and fluorescence bands as well as to decrease of the fluorescence intensity.

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Reference£º
Thiazole | C3H8509NS – PubChem,
Thiazole | chemical compound | Britannica