Ethyl 2-(3-amino-4-fluorophenyl)acetate

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Reagent Code: #41488
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CAS Number 858972-17-5

science Other reagents with same CAS 858972-17-5

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Weight 197.21 g/mol
Formula C₁₀H₁₂FNO₂
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MDL Number MFCD16620934
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description Product Description

Used primarily in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structure, featuring both an amino and a fluorine group, makes it valuable for creating molecules with potential biological activity, particularly in the development of drugs targeting neurological disorders, cancer, and inflammation. Additionally, it is employed in organic synthesis to construct complex molecules for medicinal chemistry studies, aiding in the discovery of new therapeutic agents. Its ester group also allows for further chemical modifications, enhancing its utility in drug design and optimization processes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿756.00

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Ethyl 2-(3-amino-4-fluorophenyl)acetate
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Used primarily in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structure, featuring both an amino and a fluorine group, makes it valuable for creating molecules with potential biological activity, particularly in the development of drugs targeting neurological disorders, cancer, and inflammation. Additionally, it is employed in organic synthesis to construct complex molecules for medicinal che

Used primarily in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structure, featuring both an amino and a fluorine group, makes it valuable for creating molecules with potential biological activity, particularly in the development of drugs targeting neurological disorders, cancer, and inflammation. Additionally, it is employed in organic synthesis to construct complex molecules for medicinal chemistry studies, aiding in the discovery of new therapeutic agents. Its ester group also allows for further chemical modifications, enhancing its utility in drug design and optimization processes.

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