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3-Hydroxyindolin-2-one is an oxindole and a hydroxyindole, specifically 1,3-dihydro-2H-indol-2-one with a hydroxy group at position 3.

CAS No.	61-71-2
Product Name	3-Hydroxyindolin-2-one

Irritant

Signal Word:Warning

HCode:H302-H315-H319-H335

PCode:P261-P264-P264+P265-P270-P271-P280-P301+P317-P302+P352-P304+P340-P305+P351+P338-P319-P321-P330-P332+P317-P337+P317-P362+P364-P403+P233-P405-P501

3-Hydroxyindolin-2-one

CAS No.	61-71-2
MDL No.	N/A
MF	C₈H₇NO₂
MW	149.15
InChI Key	SGZFJWQQBHYNNF-UHFFFAOYSA-N

CUSTOM SYNTHESIS PRECLINICAL SUPPORT

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Custom synthesis and bulk supply options are available upon request.

Product Information

3-Hydroxyindolin-2-one is an oxindole and a hydroxyindole, specifically 1,3-dihydro-2H-indol-2-one with a hydroxy group at position 3.

CAS No.	61-71-2
Product Name	3-Hydroxyindolin-2-one

Irritant

Signal Word:Warning

HCode:H302-H315-H319-H335

PCode:P261-P264-P264+P265-P270-P271-P280-P301+P317-P302+P352-P304+P340-P305+P351+P338-P319-P321-P330-P332+P317-P337+P317-P362+P364-P403+P233-P405-P501

3-Hydroxyindolin-2-one

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3-Hydroxyindolin-2-one

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Properties

Documentation

3-Hydroxyindolin-2-one

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A facile pathway to enantiomerically enriched 3-hydroxy-2-oxindoles: asymmetric intramolecular arylation of α-keto amides catalyzed by a palladium-DifluorPhos complex.

A competitive index assay identifies several Ralstonia solanacearum type III effector mutant strains with reduced fitness in host plants.

Quinidine thiourea-catalyzed aldol reaction of unactivated ketones: highly enantioselective synthesis of 3-alkyl-3-hydroxyindolin-2-ones.

Organocatalytic enantioselective cross-aldol reactions of aldehydes with isatins: formation of two contiguous quaternary centered 3-substituted 3-hydroxyindol-2-ones.

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3-Hydroxyindolin-2-one

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Related Articles

A facile pathway to enantiomerically enriched 3-hydroxy-2-oxindoles: asymmetric intramolecular arylation of α-keto amides catalyzed by a palladium-DifluorPhos complex.

A competitive index assay identifies several Ralstonia solanacearum type III effector mutant strains with reduced fitness in host plants.

Quinidine thiourea-catalyzed aldol reaction of unactivated ketones: highly enantioselective synthesis of 3-alkyl-3-hydroxyindolin-2-ones.

Organocatalytic enantioselective cross-aldol reactions of aldehydes with isatins: formation of two contiguous quaternary centered 3-substituted 3-hydroxyindol-2-ones.

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Documentation