Methyl 2-amino-5-bromo-3-methylbenzoate

97%

Reagent Code: #208839
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CAS Number 206548-14-3

science Other reagents with same CAS 206548-14-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 244.09 g/mol
Formula C₉H₁₀BrNO₂
badge Registry Numbers
MDL Number MFCD06797379
thermostat Physical Properties
Boiling Point 307.3±37.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of benzodiazepine derivatives and other central nervous system agents. It serves as a building block in organic synthesis due to the presence of amino, ester, and bromo functional groups on a substituted benzoate scaffold, allowing for further chemical modifications such as cross-coupling reactions or substitutions. Commonly employed in the preparation of heterocyclic compounds and bioactive molecules in medicinal chemistry research. Also utilized in the production of agrochemicals and dyes where brominated aromatic scaffolds are required.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿4,400.00
10g
10-20 days ฿8,760.00
25g
10-20 days ฿20,160.00
Methyl 2-amino-5-bromo-3-methylbenzoate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of benzodiazepine derivatives and other central nervous system agents. It serves as a building block in organic synthesis due to the presence of amino, ester, and bromo functional groups on a substituted benzoate scaffold, allowing for further chemical modifications such as cross-coupling reactions or substitutions. Commonly employed in the preparation of heterocyclic compounds and bioactive molecules in medic

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of benzodiazepine derivatives and other central nervous system agents. It serves as a building block in organic synthesis due to the presence of amino, ester, and bromo functional groups on a substituted benzoate scaffold, allowing for further chemical modifications such as cross-coupling reactions or substitutions. Commonly employed in the preparation of heterocyclic compounds and bioactive molecules in medicinal chemistry research. Also utilized in the production of agrochemicals and dyes where brominated aromatic scaffolds are required.

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