Ethyl 4-amino-3-bromo-5-iodobenzoate

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Reagent Code: #183506
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CAS Number 437707-51-2

science Other reagents with same CAS 437707-51-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 369.98 g/mol
Formula C₉H₉BrINO₂
badge Registry Numbers
MDL Number MFCD06658437
thermostat Physical Properties
Boiling Point 407.6±45.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in inert gas

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Its structure contains multiple reactive sites—bromine and iodine allow cross-coupling reactions like Suzuki or Heck reactions, enabling the construction of complex aromatic systems. The amino group can be diazotized or acylated to introduce further functionality. The ester group serves as a handle for hydrolysis or amidation, making it useful in the preparation of bioactive molecules, particularly in the development of drug candidates targeting central nervous system disorders and anti-inflammatory agents. Also employed in the synthesis of fluorescent dyes and functional materials due to its halogenated aromatic core.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿690.00
inventory 10g
10-20 days ฿5,540.00
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Ethyl 4-amino-3-bromo-5-iodobenzoate
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Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Its structure contains multiple reactive sites—bromine and iodine allow cross-coupling reactions like Suzuki or Heck reactions, enabling the construction of complex aromatic systems. The amino group can be diazotized or acylated to introduce further functionality. The ester group serves as a handle for hydrolysis or amidation, making it useful in the preparation of bioactive molecules, particularly in the development of d

Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Its structure contains multiple reactive sites—bromine and iodine allow cross-coupling reactions like Suzuki or Heck reactions, enabling the construction of complex aromatic systems. The amino group can be diazotized or acylated to introduce further functionality. The ester group serves as a handle for hydrolysis or amidation, making it useful in the preparation of bioactive molecules, particularly in the development of drug candidates targeting central nervous system disorders and anti-inflammatory agents. Also employed in the synthesis of fluorescent dyes and functional materials due to its halogenated aromatic core.

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