4-((4-(2-Chlorophenoxy)phenyl)amino)-4-oxobutanoic acid

95%

Reagent Code: #130937
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CAS Number 667446-82-4

science Other reagents with same CAS 667446-82-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 319.74 g/mol
Formula C₁₆H₁₄ClNO₄
badge Registry Numbers
MDL Number MFCD03353494
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of anti-inflammatory and kinase inhibitor compounds. Its structure supports conjugation in prodrug designs, enhancing bioavailability and targeted delivery. Also employed in research for modifying peptide-like molecules to improve metabolic stability. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to act as a linker with hydrogen bonding and hydrophobic interactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿32,000.00
inventory 1g
10-20 days ฿144,000.00

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4-((4-(2-Chlorophenoxy)phenyl)amino)-4-oxobutanoic acid
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Used in the synthesis of pharmaceutical intermediates, particularly in the development of anti-inflammatory and kinase inhibitor compounds. Its structure supports conjugation in prodrug designs, enhancing bioavailability and targeted delivery. Also employed in research for modifying peptide-like molecules to improve metabolic stability. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to act as a linker with hydrogen bonding and hydrophobic int

Used in the synthesis of pharmaceutical intermediates, particularly in the development of anti-inflammatory and kinase inhibitor compounds. Its structure supports conjugation in prodrug designs, enhancing bioavailability and targeted delivery. Also employed in research for modifying peptide-like molecules to improve metabolic stability. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to act as a linker with hydrogen bonding and hydrophobic interactions.

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