(S)-2-Amino-3-(4-((fluorosulfonyl)oxy)phenyl)propanoic acid hydrochloride

98%

Reagent Code: #233539
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CAS Number 2227199-79-1

science Other reagents with same CAS 2227199-79-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 299.7 g/mol
Formula C₉H₁₁ClFNO₅S
badge Registry Numbers
MDL Number MFCD33031933
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of positron emission tomography (PET) tracers. Its fluorosulfonyl group enables efficient radiolabeling with fluorine-18, making it valuable for creating imaging agents that target specific biological pathways, such as amino acid transport in cancer cells. The compound’s chiral structure supports selective interactions with biological systems, enhancing the accuracy of diagnostic imaging. It is also employed in the preparation of enzyme inhibitors and receptor ligands where precise molecular recognition is required.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,920.00
inventory 250mg
10-20 days ฿8,080.00
inventory 1g
10-20 days ฿16,200.00
(S)-2-Amino-3-(4-((fluorosulfonyl)oxy)phenyl)propanoic acid hydrochloride
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Used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of positron emission tomography (PET) tracers. Its fluorosulfonyl group enables efficient radiolabeling with fluorine-18, making it valuable for creating imaging agents that target specific biological pathways, such as amino acid transport in cancer cells. The compound’s chiral structure supports selective interactions with biological systems, enhancing the accuracy of diagnostic imaging. It is als

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of positron emission tomography (PET) tracers. Its fluorosulfonyl group enables efficient radiolabeling with fluorine-18, making it valuable for creating imaging agents that target specific biological pathways, such as amino acid transport in cancer cells. The compound’s chiral structure supports selective interactions with biological systems, enhancing the accuracy of diagnostic imaging. It is also employed in the preparation of enzyme inhibitors and receptor ligands where precise molecular recognition is required.

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