(S)-1-(4-Bromothiophen-2-yl)ethan-1-amine hydrochloride

98%

Reagent Code: #236913
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CAS Number 2682097-56-7

science Other reagents with same CAS 2682097-56-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 242.5644 g/mol
Formula C₆H₉BrClNS
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key chiral intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its chiral amine functionality allows for selective interactions in drug molecules, enhancing potency and reducing side effects. Commonly employed in the development of serotonin and dopamine receptor modulators. Also utilized in asymmetric synthesis due to the stereochemical purity of the (S)-enantiomer, enabling precise construction of complex medicinal agents.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,350.00
inventory 250mg
10-20 days ฿17,170.00
inventory 1g
10-20 days ฿50,080.00
(S)-1-(4-Bromothiophen-2-yl)ethan-1-amine hydrochloride
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Used as a key chiral intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its chiral amine functionality allows for selective interactions in drug molecules, enhancing potency and reducing side effects. Commonly employed in the development of serotonin and dopamine receptor modulators. Also utilized in asymmetric synthesis due to the stereochemical purity of the (S)-enantiomer, enabling precise construction of complex

Used as a key chiral intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its chiral amine functionality allows for selective interactions in drug molecules, enhancing potency and reducing side effects. Commonly employed in the development of serotonin and dopamine receptor modulators. Also utilized in asymmetric synthesis due to the stereochemical purity of the (S)-enantiomer, enabling precise construction of complex medicinal agents.

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