(S)-6-Bromo-2,3-dihydrobenzofuran-3-amine

95%

Reagent Code: #236598
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CAS Number 1228568-69-1

science Other reagents with same CAS 1228568-69-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.06 g/mol
Formula C₈H₈BrNO
badge Registry Numbers
MDL Number MFCD14562144
inventory_2 Storage & Handling
Storage 2-8°C, avoiding light

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and cardiovascular drugs. Its bromine functionality allows for further cross-coupling reactions, enabling the construction of complex molecular architectures. The presence of an amine group and a rigid benzofuran scaffold makes it valuable in medicinal chemistry for optimizing potency and selectivity in drug candidates. Commonly employed in asymmetric synthesis to introduce stereochemical control in active pharmaceutical ingredients (APIs).

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿10,100.00
inventory 100mg
10-20 days ฿17,120.00
inventory 1g
10-20 days ฿77,030.00
inventory 250mg
10-20 days ฿25,650.00
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(S)-6-Bromo-2,3-dihydrobenzofuran-3-amine
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and cardiovascular drugs. Its bromine functionality allows for further cross-coupling reactions, enabling the construction of complex molecular architectures. The presence of an amine group and a rigid benzofuran scaffold makes it valuable in medicinal chemistry for optimizing potency and selectivity in drug candidates. Commonly employed in asymmetric synthesis to introduc

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and cardiovascular drugs. Its bromine functionality allows for further cross-coupling reactions, enabling the construction of complex molecular architectures. The presence of an amine group and a rigid benzofuran scaffold makes it valuable in medicinal chemistry for optimizing potency and selectivity in drug candidates. Commonly employed in asymmetric synthesis to introduce stereochemical control in active pharmaceutical ingredients (APIs).

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