Ethyl 3-amino-3-(4-iodophenyl)propanoate, HCl

95%

Reagent Code: #44896
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CAS Number 502842-21-9

science Other reagents with same CAS 502842-21-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 355.5998 g/mol
Formula C₁₁H₁₅ClINO₂
badge Registry Numbers
MDL Number MFCD02663272
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in pharmaceutical research and development as an intermediate in the synthesis of more complex molecules. Its structure, featuring both an amino group and an iodophenyl moiety, makes it valuable for creating compounds with potential biological activity. It is often employed in the preparation of drug candidates targeting neurological disorders, as the iodophenyl group can enhance binding affinity to certain receptors. Additionally, it serves as a building block in organic synthesis, particularly in reactions involving cross-coupling or further functionalization of the aromatic ring. Its hydrochloride salt form improves stability and solubility, facilitating its use in various experimental protocols.

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Test Parameter Specification
Appearance White Powder
Purity (Titration by AgNO3) 94.5-105.5%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,921.00

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Ethyl 3-amino-3-(4-iodophenyl)propanoate, HCl
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This compound is primarily utilized in pharmaceutical research and development as an intermediate in the synthesis of more complex molecules. Its structure, featuring both an amino group and an iodophenyl moiety, makes it valuable for creating compounds with potential biological activity. It is often employed in the preparation of drug candidates targeting neurological disorders, as the iodophenyl group can enhance binding affinity to certain receptors. Additionally, it serves as a building block in orga

This compound is primarily utilized in pharmaceutical research and development as an intermediate in the synthesis of more complex molecules. Its structure, featuring both an amino group and an iodophenyl moiety, makes it valuable for creating compounds with potential biological activity. It is often employed in the preparation of drug candidates targeting neurological disorders, as the iodophenyl group can enhance binding affinity to certain receptors. Additionally, it serves as a building block in organic synthesis, particularly in reactions involving cross-coupling or further functionalization of the aromatic ring. Its hydrochloride salt form improves stability and solubility, facilitating its use in various experimental protocols.

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