Fun Route: New Discovery of 136663-38-2

Different reactions of this compound((2-Methylbenzo[d]oxazol-5-yl)methanol)Recommanded Product: 136663-38-2 require different conditions, so the reaction conditions are very important.

The preparation of ester heterocycles mostly uses heteroatoms as nucleophilic sites, which are achieved by intramolecular substitution or addition reactions. Compound: (2-Methylbenzo[d]oxazol-5-yl)methanol( cas:136663-38-2 ) is researched.Recommanded Product: 136663-38-2.Balaswamy, G.; Pradeep, P.; Srinivas, K.; Rajakomuraiah, T. published the article 《Design, synthesis and antimicrobial activity of novel 2-substituted benzoxazole derivatives》 about this compound( cas:136663-38-2 ) in International Journal of Chemical Sciences. Keywords: benzoxazole derivative preparation antimicrobial activity. Let’s learn more about this compound (cas:136663-38-2).

In the current research work, the title compounds were synthesized from Me 2-substituted benzoxazole-5-carboxylate by refluxing with methanol and THF (1 : 1) in presence of NaBH4, which afforded (2-substituted benzoxazol-5-yl)methanol, on partial oxidation with PCC furnished 2-substituted benzoxazole-5-carbaldehyde, on treatment with appropriate carbonyl compounds monoethyl malonate, Et acetoacetate or malonic acid yielded the corresponding α,β-unsaturated derivatives of 2-substituted benzoxazoles like, Et 3-(2-substituted benzoxazol-5-yl)acrylate, 4-(2-substituted benzoxazol-5-yl)but-3-en-2-one and 3-(2-substituted benzoxazol-5-yl)acrylic acid. The identification and characterization of all the synthesized compounds were confirmed by elemental anal., m.p., thin layer chromatog., FTIR, 1H NMR and mass spectral data. All the compounds were screened for antimicrobial activity. In view of interesting biol. activities and pharmacol. importance associated with benzoxazole derivatives, some of the derivatives of benzoxazole containing heterocyclic ring were prepared and their bio-potential were evaluated.

Different reactions of this compound((2-Methylbenzo[d]oxazol-5-yl)methanol)Recommanded Product: 136663-38-2 require different conditions, so the reaction conditions are very important.

Reference:
Pyrroline – Wikipedia,
1-Pyrroline | C4H7N – PubChem

Application of 136663-38-2

The article 《Design, synthesis and antimicrobial activity of novel 2-substituted benzoxazole derivatives》 also mentions many details about this compound(136663-38-2)SDS of cas: 136663-38-2, you can pay attention to it, because details determine success or failure

Epoxy compounds usually have stronger nucleophilic ability, because the alkyl group on the oxygen atom makes the bond angle smaller, which makes the lone pair of electrons react more dissimilarly with the electron-deficient system. Compound: (2-Methylbenzo[d]oxazol-5-yl)methanol, is researched, Molecular C9H9NO2, CAS is 136663-38-2, about Design, synthesis and antimicrobial activity of novel 2-substituted benzoxazole derivatives.SDS of cas: 136663-38-2.

In the current research work, the title compounds were synthesized from Me 2-substituted benzoxazole-5-carboxylate by refluxing with methanol and THF (1 : 1) in presence of NaBH4, which afforded (2-substituted benzoxazol-5-yl)methanol, on partial oxidation with PCC furnished 2-substituted benzoxazole-5-carbaldehyde, on treatment with appropriate carbonyl compounds monoethyl malonate, Et acetoacetate or malonic acid yielded the corresponding α,β-unsaturated derivatives of 2-substituted benzoxazoles like, Et 3-(2-substituted benzoxazol-5-yl)acrylate, 4-(2-substituted benzoxazol-5-yl)but-3-en-2-one and 3-(2-substituted benzoxazol-5-yl)acrylic acid. The identification and characterization of all the synthesized compounds were confirmed by elemental anal., m.p., thin layer chromatog., FTIR, 1H NMR and mass spectral data. All the compounds were screened for antimicrobial activity. In view of interesting biol. activities and pharmacol. importance associated with benzoxazole derivatives, some of the derivatives of benzoxazole containing heterocyclic ring were prepared and their bio-potential were evaluated.

The article 《Design, synthesis and antimicrobial activity of novel 2-substituted benzoxazole derivatives》 also mentions many details about this compound(136663-38-2)SDS of cas: 136663-38-2, you can pay attention to it, because details determine success or failure

Reference:
Pyrroline – Wikipedia,
1-Pyrroline | C4H7N – PubChem

Derivation of elementary reaction about 136663-38-2

The article 《Palladium-Catalyzed Direct Hydroxymethylation of Aryl Halides and Triflates with Potassium Acetoxymethyltrifluoroborate》 also mentions many details about this compound(136663-38-2)Safety of (2-Methylbenzo[d]oxazol-5-yl)methanol, you can pay attention to it, because details determine success or failure

Safety of (2-Methylbenzo[d]oxazol-5-yl)methanol. The protonation of heteroatoms in aromatic heterocycles can be divided into two categories: lone pairs of electrons are in the aromatic ring conjugated system; and lone pairs of electrons do not participate. Compound: (2-Methylbenzo[d]oxazol-5-yl)methanol, is researched, Molecular C9H9NO2, CAS is 136663-38-2, about Palladium-Catalyzed Direct Hydroxymethylation of Aryl Halides and Triflates with Potassium Acetoxymethyltrifluoroborate. Author is Murai, Norio; Yonaga, Masahiro; Tanaka, Keigo.

Suzuki-Miyaura cross-coupling reactions of aryl halides and triflates with potassium acetoxymethyltrifluoroborate afforded the corresponding aryl and heteroaryl methanol products in moderate to excellent yields.

The article 《Palladium-Catalyzed Direct Hydroxymethylation of Aryl Halides and Triflates with Potassium Acetoxymethyltrifluoroborate》 also mentions many details about this compound(136663-38-2)Safety of (2-Methylbenzo[d]oxazol-5-yl)methanol, you can pay attention to it, because details determine success or failure

Reference:
Pyrroline – Wikipedia,
1-Pyrroline | C4H7N – PubChem

New downstream synthetic route of 136663-38-2

As far as I know, this compound(136663-38-2)Formula: C9H9NO2 can be applied in many ways, which is helpful for the development of experiments. Therefore many people are doing relevant researches.

The preparation of ester heterocycles mostly uses heteroatoms as nucleophilic sites, which are achieved by intramolecular substitution or addition reactions. Compound: (2-Methylbenzo[d]oxazol-5-yl)methanol( cas:136663-38-2 ) is researched.Formula: C9H9NO2.Balaswamy, G.; Pradeep, P.; Srinivas, K.; Rajakomuraiah, T. published the article 《Design, synthesis and antimicrobial activity of novel 2-substituted benzoxazole derivatives》 about this compound( cas:136663-38-2 ) in International Journal of Chemical Sciences. Keywords: benzoxazole derivative preparation antimicrobial activity. Let’s learn more about this compound (cas:136663-38-2).

In the current research work, the title compounds were synthesized from Me 2-substituted benzoxazole-5-carboxylate by refluxing with methanol and THF (1 : 1) in presence of NaBH4, which afforded (2-substituted benzoxazol-5-yl)methanol, on partial oxidation with PCC furnished 2-substituted benzoxazole-5-carbaldehyde, on treatment with appropriate carbonyl compounds monoethyl malonate, Et acetoacetate or malonic acid yielded the corresponding α,β-unsaturated derivatives of 2-substituted benzoxazoles like, Et 3-(2-substituted benzoxazol-5-yl)acrylate, 4-(2-substituted benzoxazol-5-yl)but-3-en-2-one and 3-(2-substituted benzoxazol-5-yl)acrylic acid. The identification and characterization of all the synthesized compounds were confirmed by elemental anal., m.p., thin layer chromatog., FTIR, 1H NMR and mass spectral data. All the compounds were screened for antimicrobial activity. In view of interesting biol. activities and pharmacol. importance associated with benzoxazole derivatives, some of the derivatives of benzoxazole containing heterocyclic ring were prepared and their bio-potential were evaluated.

As far as I know, this compound(136663-38-2)Formula: C9H9NO2 can be applied in many ways, which is helpful for the development of experiments. Therefore many people are doing relevant researches.

Reference:
Pyrroline – Wikipedia,
1-Pyrroline | C4H7N – PubChem

Derivation of elementary reaction about 136663-38-2

In addition to the literature in the link below, there is a lot of literature about this compound((2-Methylbenzo[d]oxazol-5-yl)methanol)Recommanded Product: (2-Methylbenzo[d]oxazol-5-yl)methanol, illustrating the importance and wide applicability of this compound(136663-38-2).

Murai, Norio; Yonaga, Masahiro; Tanaka, Keigo published the article 《Palladium-Catalyzed Direct Hydroxymethylation of Aryl Halides and Triflates with Potassium Acetoxymethyltrifluoroborate》. Keywords: alc arylmethyl preparation coupling potassium acetoxymethyltrifluoroborate aryl halide triflate; cross coupling Suzuki Miyaura potassium acetoxymethyltrifluoroborate aryl halide triflate; hydroxymethylation acetoxymethyltrifluoroborate aryl halide triflate palladium catalyzed.They researched the compound: (2-Methylbenzo[d]oxazol-5-yl)methanol( cas:136663-38-2 ).Recommanded Product: (2-Methylbenzo[d]oxazol-5-yl)methanol. Aromatic heterocyclic compounds can be divided into two categories: single heterocyclic and fused heterocyclic. In addition, there is a lot of other information about this compound (cas:136663-38-2) here.

Suzuki-Miyaura cross-coupling reactions of aryl halides and triflates with potassium acetoxymethyltrifluoroborate afforded the corresponding aryl and heteroaryl methanol products in moderate to excellent yields.

In addition to the literature in the link below, there is a lot of literature about this compound((2-Methylbenzo[d]oxazol-5-yl)methanol)Recommanded Product: (2-Methylbenzo[d]oxazol-5-yl)methanol, illustrating the importance and wide applicability of this compound(136663-38-2).

Reference:
Pyrroline – Wikipedia,
1-Pyrroline | C4H7N – PubChem

Properties and Exciting Facts About 136663-38-2

Here is just a brief introduction to this compound(136663-38-2)Synthetic Route of C9H9NO2, more information about the compound((2-Methylbenzo[d]oxazol-5-yl)methanol) is in the article, you can click the link below.

Synthetic Route of C9H9NO2. The fused heterocycle is formed by combining a benzene ring with a single heterocycle, or two or more single heterocycles. Compound: (2-Methylbenzo[d]oxazol-5-yl)methanol, is researched, Molecular C9H9NO2, CAS is 136663-38-2, about Design, synthesis and antimicrobial activity of novel 2-substituted benzoxazole derivatives. Author is Balaswamy, G.; Pradeep, P.; Srinivas, K.; Rajakomuraiah, T..

In the current research work, the title compounds were synthesized from Me 2-substituted benzoxazole-5-carboxylate by refluxing with methanol and THF (1 : 1) in presence of NaBH4, which afforded (2-substituted benzoxazol-5-yl)methanol, on partial oxidation with PCC furnished 2-substituted benzoxazole-5-carbaldehyde, on treatment with appropriate carbonyl compounds monoethyl malonate, Et acetoacetate or malonic acid yielded the corresponding α,β-unsaturated derivatives of 2-substituted benzoxazoles like, Et 3-(2-substituted benzoxazol-5-yl)acrylate, 4-(2-substituted benzoxazol-5-yl)but-3-en-2-one and 3-(2-substituted benzoxazol-5-yl)acrylic acid. The identification and characterization of all the synthesized compounds were confirmed by elemental anal., m.p., thin layer chromatog., FTIR, 1H NMR and mass spectral data. All the compounds were screened for antimicrobial activity. In view of interesting biol. activities and pharmacol. importance associated with benzoxazole derivatives, some of the derivatives of benzoxazole containing heterocyclic ring were prepared and their bio-potential were evaluated.

Here is just a brief introduction to this compound(136663-38-2)Synthetic Route of C9H9NO2, more information about the compound((2-Methylbenzo[d]oxazol-5-yl)methanol) is in the article, you can click the link below.

Reference:
Pyrroline – Wikipedia,
1-Pyrroline | C4H7N – PubChem

Application of 136663-38-2

If you want to learn more about this compound((2-Methylbenzo[d]oxazol-5-yl)methanol)Computed Properties of C9H9NO2, you may wish to communicate with the author of the article,or consult the relevant literature related to this compound(136663-38-2).

Computed Properties of C9H9NO2. Aromatic heterocyclic compounds can also be classified according to the number of heteroatoms contained in the heterocycle: single heteroatom, two heteroatoms, three heteroatoms and four heteroatoms. Compound: (2-Methylbenzo[d]oxazol-5-yl)methanol, is researched, Molecular C9H9NO2, CAS is 136663-38-2, about Palladium-Catalyzed Direct Hydroxymethylation of Aryl Halides and Triflates with Potassium Acetoxymethyltrifluoroborate. Author is Murai, Norio; Yonaga, Masahiro; Tanaka, Keigo.

Suzuki-Miyaura cross-coupling reactions of aryl halides and triflates with potassium acetoxymethyltrifluoroborate afforded the corresponding aryl and heteroaryl methanol products in moderate to excellent yields.

If you want to learn more about this compound((2-Methylbenzo[d]oxazol-5-yl)methanol)Computed Properties of C9H9NO2, you may wish to communicate with the author of the article,or consult the relevant literature related to this compound(136663-38-2).

Reference:
Pyrroline – Wikipedia,
1-Pyrroline | C4H7N – PubChem

The effect of reaction temperature change on equilibrium 136663-38-2

I hope my short article helps more people learn about this compound((2-Methylbenzo[d]oxazol-5-yl)methanol)Electric Literature of C9H9NO2. Apart from the compound(136663-38-2), you can read my other articles to know other related compounds.

Murai, Norio; Yonaga, Masahiro; Tanaka, Keigo published the article 《Palladium-Catalyzed Direct Hydroxymethylation of Aryl Halides and Triflates with Potassium Acetoxymethyltrifluoroborate》. Keywords: alc arylmethyl preparation coupling potassium acetoxymethyltrifluoroborate aryl halide triflate; cross coupling Suzuki Miyaura potassium acetoxymethyltrifluoroborate aryl halide triflate; hydroxymethylation acetoxymethyltrifluoroborate aryl halide triflate palladium catalyzed.They researched the compound: (2-Methylbenzo[d]oxazol-5-yl)methanol( cas:136663-38-2 ).Electric Literature of C9H9NO2. Aromatic heterocyclic compounds can be divided into two categories: single heterocyclic and fused heterocyclic. In addition, there is a lot of other information about this compound (cas:136663-38-2) here.

Suzuki-Miyaura cross-coupling reactions of aryl halides and triflates with potassium acetoxymethyltrifluoroborate afforded the corresponding aryl and heteroaryl methanol products in moderate to excellent yields.

I hope my short article helps more people learn about this compound((2-Methylbenzo[d]oxazol-5-yl)methanol)Electric Literature of C9H9NO2. Apart from the compound(136663-38-2), you can read my other articles to know other related compounds.

Reference:
Pyrroline – Wikipedia,
1-Pyrroline | C4H7N – PubChem

Derivation of elementary reaction about 136663-38-2

From this literature《Palladium-Catalyzed Direct Hydroxymethylation of Aryl Halides and Triflates with Potassium Acetoxymethyltrifluoroborate》,we know some information about this compound(136663-38-2)Name: (2-Methylbenzo[d]oxazol-5-yl)methanol, but this is not all information, there are many literatures related to this compound(136663-38-2).

Epoxy compounds usually have stronger nucleophilic ability, because the alkyl group on the oxygen atom makes the bond angle smaller, which makes the lone pair of electrons react more dissimilarly with the electron-deficient system. Compound: (2-Methylbenzo[d]oxazol-5-yl)methanol, is researched, Molecular C9H9NO2, CAS is 136663-38-2, about Palladium-Catalyzed Direct Hydroxymethylation of Aryl Halides and Triflates with Potassium Acetoxymethyltrifluoroborate.Name: (2-Methylbenzo[d]oxazol-5-yl)methanol.

Suzuki-Miyaura cross-coupling reactions of aryl halides and triflates with potassium acetoxymethyltrifluoroborate afforded the corresponding aryl and heteroaryl methanol products in moderate to excellent yields.

From this literature《Palladium-Catalyzed Direct Hydroxymethylation of Aryl Halides and Triflates with Potassium Acetoxymethyltrifluoroborate》,we know some information about this compound(136663-38-2)Name: (2-Methylbenzo[d]oxazol-5-yl)methanol, but this is not all information, there are many literatures related to this compound(136663-38-2).

Reference:
Pyrroline – Wikipedia,
1-Pyrroline | C4H7N – PubChem