Methyl2-(4-bromophenyl)propanoate

97%

Reagent Code: #214079
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CAS Number 83636-46-8

science Other reagents with same CAS 83636-46-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 243.1 g/mol
Formula C₁₀H₁₁BrO₂
badge Registry Numbers
MDL Number MFCD18908971
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and fine chemicals. The bromine substituent allows for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex aromatic compounds. The ester group can be hydrolyzed to the corresponding carboxylic acid or reduced to an alcohol, offering versatility in functional group transformations. Commonly employed in the development of active pharmaceutical ingredients (APIs) where a substituted phenylpropanoate scaffold is required. Also utilized in the preparation of agrochemicals and specialty polymers due to its reactive handle and structural stability.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿7,360.00
250mg
10-20 days ฿10,560.00
1g
10-20 days ฿27,000.00
Methyl2-(4-bromophenyl)propanoate
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Used in organic synthesis as an intermediate for pharmaceuticals and fine chemicals. The bromine substituent allows for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex aromatic compounds. The ester group can be hydrolyzed to the corresponding carboxylic acid or reduced to an alcohol, offering versatility in functional group transformations. Commonly employed in the development of active pharmaceutical ingredients (APIs) where a substituted phenylpropanoate

Used in organic synthesis as an intermediate for pharmaceuticals and fine chemicals. The bromine substituent allows for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex aromatic compounds. The ester group can be hydrolyzed to the corresponding carboxylic acid or reduced to an alcohol, offering versatility in functional group transformations. Commonly employed in the development of active pharmaceutical ingredients (APIs) where a substituted phenylpropanoate scaffold is required. Also utilized in the preparation of agrochemicals and specialty polymers due to its reactive handle and structural stability.

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