N-(3-(2-Bromoacetyl)phenyl)methanesulfonamide

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Reagent Code: #215589
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CAS Number 2065-04-5

science Other reagents with same CAS 2065-04-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 292.15 g/mol
Formula C₉H₁₀BrNO₃S
badge Registry Numbers
MDL Number MFCD11052994
thermostat Physical Properties
Melting Point 124.5-124.6 °C
Boiling Point 406.4±51.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.672±0.06 g/cm3(Predicted)
Storage Room temperature, seal, inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its reactive bromoacetyl group allows for selective alkylation, enabling the formation of covalent bonds with target proteins. Commonly employed in medicinal chemistry for structure-activity relationship studies due to its ability to enhance binding affinity and selectivity. Also utilized in the preparation of labeled probes for biochemical assays and target validation.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,950.00
inventory 250mg
10-20 days ฿16,900.00

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N-(3-(2-Bromoacetyl)phenyl)methanesulfonamide
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its reactive bromoacetyl group allows for selective alkylation, enabling the formation of covalent bonds with target proteins. Commonly employed in medicinal chemistry for structure-activity relationship studies due to its ability to enhance binding affinity and selectivity. Also utilized in the preparation of labeled probes for biochemical assays and target val

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its reactive bromoacetyl group allows for selective alkylation, enabling the formation of covalent bonds with target proteins. Commonly employed in medicinal chemistry for structure-activity relationship studies due to its ability to enhance binding affinity and selectivity. Also utilized in the preparation of labeled probes for biochemical assays and target validation.

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