H-Phg(4-OH)-OEt

98%

Reagent Code: #105201
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CAS Number 43189-39-5

science Other reagents with same CAS 43189-39-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 195.22 g/mol
Formula C₁₀H₁₃NO₃
badge Registry Numbers
MDL Number MFCD10566158
thermostat Physical Properties
Boiling Point 576.4 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dark, inert gas

description Product Description

This compound is primarily utilized in the synthesis of peptides and pharmaceuticals, serving as a key intermediate in the production of various bioactive molecules. Its structure, featuring a hydroxyl group, makes it valuable in the development of drugs targeting specific biological pathways, such as enzyme inhibitors or receptor modulators. Additionally, it is employed in the preparation of chiral compounds, where its stereochemistry plays a crucial role in achieving desired enantioselectivity. In research, it is often used to study peptide interactions and to design novel therapeutic agents. Its applications extend to the field of organic synthesis, where it acts as a building block for complex molecules with potential medicinal properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,500.00

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H-Phg(4-OH)-OEt
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This compound is primarily utilized in the synthesis of peptides and pharmaceuticals, serving as a key intermediate in the production of various bioactive molecules. Its structure, featuring a hydroxyl group, makes it valuable in the development of drugs targeting specific biological pathways, such as enzyme inhibitors or receptor modulators. Additionally, it is employed in the preparation of chiral compounds, where its stereochemistry plays a crucial role in achieving desired enantioselectivity. In rese

This compound is primarily utilized in the synthesis of peptides and pharmaceuticals, serving as a key intermediate in the production of various bioactive molecules. Its structure, featuring a hydroxyl group, makes it valuable in the development of drugs targeting specific biological pathways, such as enzyme inhibitors or receptor modulators. Additionally, it is employed in the preparation of chiral compounds, where its stereochemistry plays a crucial role in achieving desired enantioselectivity. In research, it is often used to study peptide interactions and to design novel therapeutic agents. Its applications extend to the field of organic synthesis, where it acts as a building block for complex molecules with potential medicinal properties.

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