8-Bromo-3,4-dihydro-2H-benzo[1,4]oxazine-2-carboxylic acid ethyl ester

95%

Reagent Code: #150149
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CAS Number 1021859-84-6

science Other reagents with same CAS 1021859-84-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 286.12 g/mol
Formula C₁₁H₁₂BrNO₃
badge Registry Numbers
MDL Number MFCD27992132
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system agents. It serves as a building block for heterocyclic compounds with potential biological activity, including serotonin and dopamine receptor modulators. Commonly employed in medicinal chemistry for structure-activity relationship studies due to the bromo substituent allowing further functionalization via cross-coupling reactions. Also utilized in the preparation of kinase inhibitors and other bioactive molecules in research settings.

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inventory 1g
10-20 days ฿57,790.00

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8-Bromo-3,4-dihydro-2H-benzo[1,4]oxazine-2-carboxylic acid ethyl ester
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system agents. It serves as a building block for heterocyclic compounds with potential biological activity, including serotonin and dopamine receptor modulators. Commonly employed in medicinal chemistry for structure-activity relationship studies due to the bromo substituent allowing further functionalization via cross-coupling reactions. Also utilized in the preparation of kinase inhi

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system agents. It serves as a building block for heterocyclic compounds with potential biological activity, including serotonin and dopamine receptor modulators. Commonly employed in medicinal chemistry for structure-activity relationship studies due to the bromo substituent allowing further functionalization via cross-coupling reactions. Also utilized in the preparation of kinase inhibitors and other bioactive molecules in research settings.

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