N-((5-bromothiophen-2-yl)methyl)-2-methylpropan-1-amine

≥95%

Reagent Code: #220452
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CAS Number 1019531-99-7

science Other reagents with same CAS 1019531-99-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 248.18 g/mol
Formula C₉H₁₄BrNS
badge Registry Numbers
MDL Number MFCD11139773
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of receptor antagonists and kinase inhibitors. Its structure supports binding interactions in biological targets related to inflammatory and neurological pathways. Commonly employed in medicinal chemistry for lead optimization due to the bromothiophene moiety’s versatility in cross-coupling reactions, enabling rapid derivatization. Also applied in the preparation of labeled analogs for metabolic and binding studies.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿29,330.00
N-((5-bromothiophen-2-yl)methyl)-2-methylpropan-1-amine
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of receptor antagonists and kinase inhibitors. Its structure supports binding interactions in biological targets related to inflammatory and neurological pathways. Commonly employed in medicinal chemistry for lead optimization due to the bromothiophene moiety’s versatility in cross-coupling reactions, enabling rapid derivatization. Also applied in the preparation of labeled analogs for metabolic and bind

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of receptor antagonists and kinase inhibitors. Its structure supports binding interactions in biological targets related to inflammatory and neurological pathways. Commonly employed in medicinal chemistry for lead optimization due to the bromothiophene moiety’s versatility in cross-coupling reactions, enabling rapid derivatization. Also applied in the preparation of labeled analogs for metabolic and binding studies.

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