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Structure of 156136-55-9
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6-Chloro-1-methylindolin-2-one features a chlorinated indolinone core with enhanced electronic properties from the electron-withdrawing chlorine at the 6-position. This bench-stable scaffold integrates readily into medicinal chemistry libraries, offering improved metabolic stability and solubility in polar solvents. The methyl group at nitrogen enhances lipophilicity and target engagement potential.
6-Chloro-1-methylindolin-2-one serves as a versatile scaffold for medicinal chemistry and process development, enabling efficient access to substituted indolines via palladium-catalyzed cross-coupling. The chloro group at the 6-position facilitates direct functionalization, while the lactam carbonyl and methyl substituent provide favorable polarity and metabolic stability. Its bench-stable crystalline form simplifies handling and purification in multi-step syntheses.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P280-P302+P352
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Lot numbers can be found on the outside label of a product: