2-(3-chlorophenyl)-2-methylpropanoic acid

95%

Reagent Code: #162244
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CAS Number 64798-35-2

science Other reagents with same CAS 64798-35-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 198.04 g/mol
Formula C₁₀H₁₁ClO₂
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for incorporation into more complex molecules, particularly in the development of active ingredients in herbicides and anti-inflammatory agents. The chlorophenyl group enhances lipophilicity, improving membrane permeability in drug design. Also utilized in research for creating analogs of nonsteroidal anti-inflammatory drugs (NSAIDs) due to its carboxylic acid functionality and aromatic substitution pattern.

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Test Parameter Specification
Appearance White Solid
Purity (%) 94.5-100%
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,358.50
inventory 1g
10-20 days ฿7,060.00

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2-(3-chlorophenyl)-2-methylpropanoic acid
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for incorporation into more complex molecules, particularly in the development of active ingredients in herbicides and anti-inflammatory agents. The chlorophenyl group enhances lipophilicity, improving membrane permeability in drug design. Also utilized in research for creating analogs of nonsteroidal anti-inflammatory drugs (NSAIDs) due to its carboxylic acid functionality and aromatic substitution patter

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for incorporation into more complex molecules, particularly in the development of active ingredients in herbicides and anti-inflammatory agents. The chlorophenyl group enhances lipophilicity, improving membrane permeability in drug design. Also utilized in research for creating analogs of nonsteroidal anti-inflammatory drugs (NSAIDs) due to its carboxylic acid functionality and aromatic substitution pattern.

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