Ethyl 2-amino-3-bromobenzoate

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Reagent Code: #183676
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CAS Number 1342707-37-2

science Other reagents with same CAS 1342707-37-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 244.09 g/mol
Formula C₉H₁₀BrNO₂
badge Registry Numbers
MDL Number MFCD11042861
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in inert gas

description Product Description

Used primarily as an intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing more complex molecules. It serves as a building block in the preparation of heterocyclic compounds, including benzodiazepines and other bioactive agents. Its amino and ester functional groups allow for versatile chemical modifications, making it valuable in the development of dyes, agrochemicals, and specialty chemicals. The bromine substituent enables cross-coupling reactions, facilitating the introduction of additional molecular fragments in drug discovery pathways.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,920.00
inventory 1g
10-20 days ฿5,770.00
inventory 5g
10-20 days ฿20,210.00

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Ethyl 2-amino-3-bromobenzoate
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Used primarily as an intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing more complex molecules. It serves as a building block in the preparation of heterocyclic compounds, including benzodiazepines and other bioactive agents. Its amino and ester functional groups allow for versatile chemical modifications, making it valuable in the development of dyes, agrochemicals, and specialty chemicals. The bromine substituent enables cross-coupling reactions, facilitatin

Used primarily as an intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing more complex molecules. It serves as a building block in the preparation of heterocyclic compounds, including benzodiazepines and other bioactive agents. Its amino and ester functional groups allow for versatile chemical modifications, making it valuable in the development of dyes, agrochemicals, and specialty chemicals. The bromine substituent enables cross-coupling reactions, facilitating the introduction of additional molecular fragments in drug discovery pathways.

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