6-Bromo-5-fluoro-3,3-dimethylindolin-2-one

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Reagent Code: #155261
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CAS Number 1379313-54-8

science Other reagents with same CAS 1379313-54-8

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Weight 258.09 g/mol
Formula C₁₀H₉BrFNO
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Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports selective binding to enzyme targets, making it valuable in drug discovery. Commonly employed in research settings to design molecules with antitumor and anti-inflammatory activity. Also utilized in organic synthesis to build complex heterocyclic systems due to its reactive halogen groups, which allow for further functionalization through cross-coupling reactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,530.00
inventory 250mg
10-20 days ฿17,330.00
inventory 500mg
10-20 days ฿27,720.00
inventory 1g
10-20 days ฿41,600.00
inventory 5g
10-20 days ฿82,020.00

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6-Bromo-5-fluoro-3,3-dimethylindolin-2-one
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports selective binding to enzyme targets, making it valuable in drug discovery. Commonly employed in research settings to design molecules with antitumor and anti-inflammatory activity. Also utilized in organic synthesis to build complex heterocyclic systems due to its reactive halogen groups, which allow for further functionalization throug

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports selective binding to enzyme targets, making it valuable in drug discovery. Commonly employed in research settings to design molecules with antitumor and anti-inflammatory activity. Also utilized in organic synthesis to build complex heterocyclic systems due to its reactive halogen groups, which allow for further functionalization through cross-coupling reactions.

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