3-(1-Carboxyethyl)benzoic acid

95%

Reagent Code: #157050
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CAS Number 68432-95-1

science Other reagents with same CAS 68432-95-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 194.18 g/mol
Formula C₁₀H₁₀O₄
badge Registry Numbers
MDL Number MFCD10565989
inventory_2 Storage & Handling
Storage 2-8°C, Sealed

description Product Description

Used in the synthesis of specialty polymers and pharmaceutical intermediates, this compound serves as a building block in organic reactions where dicarboxylic acid functionality is required. Its aromatic and aliphatic carboxylic groups allow for selective esterification or amidation, making it valuable in developing active pharmaceutical ingredients (APIs) and prodrugs. It is also employed in the preparation of ligands for metal-organic frameworks (MOFs) due to its ability to chelate metal ions. Additionally, it finds use in research settings for designing novel biodegradable materials and functional resins.

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Size Availability Unit Price Quantity
inventory 1mg
10-20 days ฿3,600.00
inventory 5mg
10-20 days ฿12,620.00

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3-(1-Carboxyethyl)benzoic acid
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Used in the synthesis of specialty polymers and pharmaceutical intermediates, this compound serves as a building block in organic reactions where dicarboxylic acid functionality is required. Its aromatic and aliphatic carboxylic groups allow for selective esterification or amidation, making it valuable in developing active pharmaceutical ingredients (APIs) and prodrugs. It is also employed in the preparation of ligands for metal-organic frameworks (MOFs) due to its ability to chelate metal ions. Additionall
Used in the synthesis of specialty polymers and pharmaceutical intermediates, this compound serves as a building block in organic reactions where dicarboxylic acid functionality is required. Its aromatic and aliphatic carboxylic groups allow for selective esterification or amidation, making it valuable in developing active pharmaceutical ingredients (APIs) and prodrugs. It is also employed in the preparation of ligands for metal-organic frameworks (MOFs) due to its ability to chelate metal ions. Additionally, it finds use in research settings for designing novel biodegradable materials and functional resins.
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