Methyl 2-(3-bromophenyl)-2-oxoacetate

≥95%

Reagent Code: #209019
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CAS Number 81316-36-1

science Other reagents with same CAS 81316-36-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 243.05 g/mol
Formula C₉H₇BrO₃
badge Registry Numbers
MDL Number MFCD11973930
inventory_2 Storage & Handling
Storage 2-8°C, dry seal

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules with potential anticonvulsant and anti-inflammatory properties. It serves as a building block in organic synthesis, enabling the construction of complex heterocyclic structures. Its bromo-substituted aromatic ring allows for further functionalization via cross-coupling reactions, making it valuable in medicinal chemistry and drug discovery research. Also employed in the preparation of analogs for structure-activity relationship (SAR) studies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,860.00
inventory 250mg
10-20 days ฿8,500.00
inventory 1g
10-20 days ฿21,260.00

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Methyl 2-(3-bromophenyl)-2-oxoacetate
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules with potential anticonvulsant and anti-inflammatory properties. It serves as a building block in organic synthesis, enabling the construction of complex heterocyclic structures. Its bromo-substituted aromatic ring allows for further functionalization via cross-coupling reactions, making it valuable in medicinal chemistry and drug discovery research. Also employed in the preparation
Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules with potential anticonvulsant and anti-inflammatory properties. It serves as a building block in organic synthesis, enabling the construction of complex heterocyclic structures. Its bromo-substituted aromatic ring allows for further functionalization via cross-coupling reactions, making it valuable in medicinal chemistry and drug discovery research. Also employed in the preparation of analogs for structure-activity relationship (SAR) studies.
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