Substance
ID:342164
Names and Identifiers
IUPAC name
2,3-dihydro-1H-indole-2,3-dione
IUPAC Traditional name
isatin
Synonyms
2,3-Indolinedioneo-Aminobenzoylformic anhydrideNSC 9262吲哚-2,3-二酮Isatin2,3-DioxoindolineIsatinic acid anhydrideIsatic acid lactam靛红2,3-Dioxo-2,3-dihydroindoleIsatine2,3-Diketoindoline
Registration numbers
MDL Number
EC Number
CAS Number
Beilstein Number
PubChem SID
Properties
Safety Information
European Hazard Symbols
Irritant (Xi)RTECS
NL7873000
Safety Statements
26-36
German water hazard class
1
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
GHS Signal Word
Warning
MSDS Link
Risk Statements
36/37/38
GHS Hazard statements
H315-H319-H335
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
GHS Precautionary statements
P261-P305+P351+P338
Product Information
Empirical Formula (Hill Notation)
C8H5NO2
Purity
98%
Physical Property
Melting Point
193-195 °C (dec.)(lit.)
Molecule Details
Packaging
100, 500 g in poly bottle
5 g in glass bottle
Application
Reactant for preparation of:
• Phthalazinone derivatives1
• Spirooxindole derivatives2
• Agents against multidrug-resistant cells expressing P-glycoprotein3
• Thiazolidinones spiro-fused to indolin-2-ones as potent and selective inhibitors of Mycobacterium tuberculosis protein tyrosine phosphatase B4
• Triazole-isatine compounds as potential antibacterial and antifungal agents5
• Biologically relevant scaffolds such as spiro[indole-thiazolidinones]6Reactant for:
• Cascade reactions with heterocyclic ketene aminals7
• Knoevenagel condensation reactions8
100, 500 g in poly bottle
5 g in glass bottle
Application
Reactant for preparation of:
• Phthalazinone derivatives1
• Spirooxindole derivatives2
• Agents against multidrug-resistant cells expressing P-glycoprotein3
• Thiazolidinones spiro-fused to indolin-2-ones as potent and selective inhibitors of Mycobacterium tuberculosis protein tyrosine phosphatase B4
• Triazole-isatine compounds as potential antibacterial and antifungal agents5
• Biologically relevant scaffolds such as spiro[indole-thiazolidinones]6Reactant for:
• Cascade reactions with heterocyclic ketene aminals7
• Knoevenagel condensation reactions8
Molecular Spectra
No Data Available
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References
No Data Available
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