(E)-3-((tert-Butoxycarbonyl)(isopropyl)amino)-2-(4-chlorophenyl)acrylic acid

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Reagent Code: #37244
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CAS Number 1489004-27-4

science Other reagents with same CAS 1489004-27-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 339.81 g/mol
Formula C₁₇H₂₂ClNO₄
badge Registry Numbers
MDL Number MFCD29078977
thermostat Physical Properties
Boiling Point 437.0±45.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs) for therapeutic drugs. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a chlorophenyl moiety, makes it a valuable building block in organic synthesis. It is often employed in peptide coupling reactions, where the Boc group provides temporary protection for amines during multi-step synthetic processes. Additionally, the presence of the chlorophenyl group can enhance the biological activity of the final compound, making it useful in the design of drugs targeting specific receptors or enzymes. Its application is also seen in medicinal chemistry research for the development of compounds with potential anti-inflammatory, antiviral, or anticancer properties.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,341.00
inventory 250mg
10-20 days ฿522.00

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(E)-3-((tert-Butoxycarbonyl)(isopropyl)amino)-2-(4-chlorophenyl)acrylic acid
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This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs) for therapeutic drugs. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a chlorophenyl moiety, makes it a valuable building block in organic synthesis. It is often employed in peptide coupling reactions, where the Boc group provides temporary protection for amines during multi-step synthetic processes. Additionally, the

This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs) for therapeutic drugs. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a chlorophenyl moiety, makes it a valuable building block in organic synthesis. It is often employed in peptide coupling reactions, where the Boc group provides temporary protection for amines during multi-step synthetic processes. Additionally, the presence of the chlorophenyl group can enhance the biological activity of the final compound, making it useful in the design of drugs targeting specific receptors or enzymes. Its application is also seen in medicinal chemistry research for the development of compounds with potential anti-inflammatory, antiviral, or anticancer properties.

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