4-BroMo-2-cyanoMethylbenzoic acid Methyl ester

≥95%

Reagent Code: #149748
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CAS Number 1083181-36-5

science Other reagents with same CAS 1083181-36-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 254.08 g/mol
Formula C₁₀H₈BrNO₂
thermostat Physical Properties
Boiling Point 393.7±32.0℃(Predicted)
inventory_2 Storage & Handling
Density 1.497±0.06 g/cm3(Predicted)
Storage 2-8℃, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where bromo and cyano functional groups allow for further chemical modifications. Its methyl ester functionality, which can be hydrolyzed to the corresponding carboxylic acid, makes it suitable for coupling reactions in organic synthesis. Commonly employed in the preparation of heterocyclic compounds and in medicinal chemistry for constructing complex drug-like molecules. Also utilized in research settings for the development of new bioactive compounds and agrochemicals due to its versatile reactivity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿800.00
inventory 250mg
10-20 days ฿1,360.00
inventory 1g
10-20 days ฿3,620.00
inventory 5g
10-20 days ฿14,290.00

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4-BroMo-2-cyanoMethylbenzoic acid Methyl ester
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where bromo and cyano functional groups allow for further chemical modifications. Its methyl ester functionality, which can be hydrolyzed to the corresponding carboxylic acid, makes it suitable for coupling reactions in organic synthesis. Commonly employed in the preparation of heterocyclic compounds and in medicinal chemistry for constructing complex drug-like molecule

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where bromo and cyano functional groups allow for further chemical modifications. Its methyl ester functionality, which can be hydrolyzed to the corresponding carboxylic acid, makes it suitable for coupling reactions in organic synthesis. Commonly employed in the preparation of heterocyclic compounds and in medicinal chemistry for constructing complex drug-like molecules. Also utilized in research settings for the development of new bioactive compounds and agrochemicals due to its versatile reactivity.

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