Methyl2-amino-5-bromo-4-(trifluoromethyl)benzoate

98%

Reagent Code: #213748
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CAS Number 851045-83-5

science Other reagents with same CAS 851045-83-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 298.06 g/mol
Formula C₉H₇BrF₃NO₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and central nervous system agents. Its structure supports the creation of more complex molecules through functional group transformations, especially leveraging the amino and ester groups for coupling reactions. The presence of bromine allows for further modifications via cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations. Also employed in agrochemical research for designing novel pesticides due to the trifluoromethyl group’s metabolic stability and lipophilicity. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿22,250.00
Methyl2-amino-5-bromo-4-(trifluoromethyl)benzoate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and central nervous system agents. Its structure supports the creation of more complex molecules through functional group transformations, especially leveraging the amino and ester groups for coupling reactions. The presence of bromine allows for further modifications via cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations. Also employed in agrochemical research for desi

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and central nervous system agents. Its structure supports the creation of more complex molecules through functional group transformations, especially leveraging the amino and ester groups for coupling reactions. The presence of bromine allows for further modifications via cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations. Also employed in agrochemical research for designing novel pesticides due to the trifluoromethyl group’s metabolic stability and lipophilicity. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies.

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