(R)-3-Amino-3-(3-bromophenyl)propan-1-ol

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Reagent Code: #228665
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CAS Number 1213827-47-4

science Other reagents with same CAS 1213827-47-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.1 g/mol
Formula C₉H₁₂NOBr
badge Registry Numbers
MDL Number MFCD07784054
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. Its structural features make it valuable for creating enantiomerically pure compounds, especially in the design of antidepressants and anticonvulsants. The presence of both amine and alcohol functional groups allows for versatile chemical modifications, facilitating its incorporation into more complex molecules. Commonly employed in medicinal chemistry for structure-activity relationship studies due to the bromophenyl group, which can be further functionalized via cross-coupling reactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,120.00
inventory 1g
10-20 days ฿23,430.00

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(R)-3-Amino-3-(3-bromophenyl)propan-1-ol
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. Its structural features make it valuable for creating enantiomerically pure compounds, especially in the design of antidepressants and anticonvulsants. The presence of both amine and alcohol functional groups allows for versatile chemical modifications, facilitating its incorporation into more complex molecules. Commonly employed in medicinal chemistry for structure-activ

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. Its structural features make it valuable for creating enantiomerically pure compounds, especially in the design of antidepressants and anticonvulsants. The presence of both amine and alcohol functional groups allows for versatile chemical modifications, facilitating its incorporation into more complex molecules. Commonly employed in medicinal chemistry for structure-activity relationship studies due to the bromophenyl group, which can be further functionalized via cross-coupling reactions.

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