6-Bromo-5-methyl-2,3-dihydro-1H-indol-2-one

98%

Reagent Code: #140821
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CAS Number 1260851-75-9

science Other reagents with same CAS 1260851-75-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 226.07 g/mol
Formula C₉H₈BrNO
badge Registry Numbers
MDL Number MFCD15525651
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its reactive bromo and indolinone functionalities, enabling coupling reactions such as Suzuki or Buchwald-Hartwig aminations. Its structure is valuable in designing bioactive molecules targeting neurological disorders and inflammatory diseases. Also employed in research settings for generating compound libraries in drug discovery programs.

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1g
10-20 days ฿58,180.00

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6-Bromo-5-methyl-2,3-dihydro-1H-indol-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. It serves as a building block in medicinal chemistry due to its reactive bromo and indolinone functionalities, enabling coupling reactions such as Suzuki or Buchwald-Hartwig aminations. Its structure is valuable in designing bioactive molecules targeting neurological disorders and inflammatory diseases. Also employed in research settings for generating compou

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its reactive bromo and indolinone functionalities, enabling coupling reactions such as Suzuki or Buchwald-Hartwig aminations. Its structure is valuable in designing bioactive molecules targeting neurological disorders and inflammatory diseases. Also employed in research settings for generating compound libraries in drug discovery programs.

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