Nombre del producto:4-Methyl-3-oxo-3,4-dihydro-2H-benzo[b][1,4]oxazine-7-boronic Acid

IUPAC Name:(4-methyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazin-7-yl)boronic acid

CAS:1515875-37-2
Fórmula molecular:C9H10BNO4
Pureza:95%+
Número de catálogo:CM386131
Peso molecular:206.99

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CM386131-1g 3-4 Weeks Ȥœƴ
CM386131-5g 5-6 Weeks şȤşȤ

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Detalles del producto

Núm. De CAS :1515875-37-2
Fórmula molecular:C9H10BNO4
Punto de fusión:-
Código de sonrisas:CN1C(=O)COC2=CC(=CC=C12)B(O)O
Densidad:
Número de catálogo:CM386131
Peso molecular:206.99
Punto de ebullición:
Nº Mdl:
Almacenamiento:

Category Infos

Benzoxazines
Benzoxazines are a type of heterocyclic compounds consisting of benzene and oxazine rings. Benzoxazine research is developing rapidly because of the many potential applications of the materials.

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Product Overview 4-Methyl-3-oxo-3,4-dihydro-2H-benzo[b][1,4]oxazine-7-boronic Acid, also known as MBOB, is a boronic acid derivative that has gained significant attention in recent years due to its potential applications in medicinal chemistry. MBOB is a heterocyclic compound that contains both boronic acid and oxazine moieties, making it a versatile molecule for various chemical reactions.
Synthesis and Application The synthesis of 4-Methyl-3-oxo-3,4-dihydro-2H-benzo[b][1,4]oxazine-7-boronic Acid involves the condensation reaction of 2-amino-4-methylphenol with salicylic aldehyde in the presence of boron trifluoride etherate. The resulting intermediate is then treated with sodium borohydride to obtain 4-Methyl-3-oxo-3,4-dihydro-2H-benzo[b][1,4]oxazine-7-boronic Acid. The yield of 4-Methyl-3-oxo-3,4-dihydro-2H-benzo[b][1,4]oxazine-7-boronic Acid can be improved by optimizing the reaction conditions, such as the reaction time, temperature, and solvent. 4-Methyl-3-oxo-3,4-dihydro-2H-benzo[b][1,4]oxazine-7-boronic Acid has been studied for its potential applications in medicinal chemistry, particularly as an antitumor agent. 4-Methyl-3-oxo-3,4-dihydro-2H-benzo[b][1,4]oxazine-7-boronic Acid has been shown to inhibit the growth of various cancer cell lines, including breast, lung, and colon cancer cells. 4-Methyl-3-oxo-3,4-dihydro-2H-benzo[b][1,4]oxazine-7-boronic Acid exerts its antitumor activity by inducing apoptosis, inhibiting cell proliferation, and suppressing tumor angiogenesis. 4-Methyl-3-oxo-3,4-dihydro-2H-benzo[b][1,4]oxazine-7-boronic Acid has also been investigated for its antibacterial and antifungal properties.
Future Directions Future research on 4-Methyl-3-oxo-3,4-dihydro-2H-benzo[b][1,4]oxazine-7-boronic Acid could focus on improving its pharmacokinetic properties, such as increasing its half-life and bioavailability. Other future directions could include investigating the potential of 4-Methyl-3-oxo-3,4-dihydro-2H-benzo[b][1,4]oxazine-7-boronic Acid as a combination therapy with other antitumor agents or exploring its antibacterial and antifungal properties further. Additionally, the mechanism of action of 4-Methyl-3-oxo-3,4-dihydro-2H-benzo[b][1,4]oxazine-7-boronic Acid could be elucidated further to better understand its antitumor activity.