(S)-2-Amino-3-fluoropropan-1-ol hydrochloride

95%

Reagent Code: #236875
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CAS Number 2413847-51-3

science Other reagents with same CAS 2413847-51-3

blur_circular Chemical Specifications

inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of fluorinated analogs of biologically active molecules. Its structure supports the creation of protease inhibitors and kinase inhibitors, making it valuable in drug discovery for cancer and antiviral therapies. The presence of both amine and alcohol functional groups allows for versatile chemical modifications, enabling coupling reactions and the formation of amides, esters, or heterocycles. Commonly employed in medicinal chemistry for optimizing metabolic stability and binding affinity in lead compounds.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿14,080.00
inventory 250mg
10-20 days ฿28,960.00
inventory 1g
10-20 days ฿57,930.00
inventory 100mg
10-20 days ฿21,780.00
(S)-2-Amino-3-fluoropropan-1-ol hydrochloride
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of fluorinated analogs of biologically active molecules. Its structure supports the creation of protease inhibitors and kinase inhibitors, making it valuable in drug discovery for cancer and antiviral therapies. The presence of both amine and alcohol functional groups allows for versatile chemical modifications, enabling coupling reactions and the formation of amides, esters, or heterocycles. Commonly emp

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of fluorinated analogs of biologically active molecules. Its structure supports the creation of protease inhibitors and kinase inhibitors, making it valuable in drug discovery for cancer and antiviral therapies. The presence of both amine and alcohol functional groups allows for versatile chemical modifications, enabling coupling reactions and the formation of amides, esters, or heterocycles. Commonly employed in medicinal chemistry for optimizing metabolic stability and binding affinity in lead compounds.

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