6-amino-1,3,3-trimethyl-2,3-dihydro-1H-indol-2-one

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Reagent Code: #196876
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CAS Number 120791-60-8

science Other reagents with same CAS 120791-60-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 190.246 g/mol
Formula C₁₁H₁₄N₂O
badge Registry Numbers
MDL Number MFCD17015856
inventory_2 Storage & Handling
Storage 2-8°C, argon-filled

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of bioactive molecules due to its indole-like structure, which is common in many drugs targeting neurological and inflammatory conditions. Also employed in research for designing novel compounds with potential antimicrobial and antiviral properties. Its amine functionality allows for easy modification, making it valuable in medicinal chemistry for structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿102,970.00

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6-amino-1,3,3-trimethyl-2,3-dihydro-1H-indol-2-one
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Used in the synthesis of pharmaceutical intermediates, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of bioactive molecules due to its indole-like structure, which is common in many drugs targeting neurological and inflammatory conditions. Also employed in research for designing novel compounds with potential antimicrobial and antiviral properties. Its amine functionality allows for easy modification, making it valuable in medi

Used in the synthesis of pharmaceutical intermediates, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of bioactive molecules due to its indole-like structure, which is common in many drugs targeting neurological and inflammatory conditions. Also employed in research for designing novel compounds with potential antimicrobial and antiviral properties. Its amine functionality allows for easy modification, making it valuable in medicinal chemistry for structure-activity relationship studies.

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