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5-Nitro-2-oxindole_Molecular_structure_CAS_20870-79-5)
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5-Nitro-2-oxindole

Catalog No. 653683 Name Sigma Aldrich
CAS Number 20870-79-5 Website http://www.sigmaaldrich.com
M. F. C8H6N2O3 Telephone 1-800-521-8956
M. W. 178.14484 Fax
Purity 97% Email
Storage Chembase ID: 74807

SYNONYMS

Title
5-硝基吲哚-2-酮
IUPAC name
5-nitro-2,3-dihydro-1H-indol-2-one
IUPAC Traditional name
5-nitro-1,3-dihydroindol-2-one
Synonyms
5-Nitro-1,3-dihydroindole-2-one
NSC 25199
NSC 99066
5-硝基-1,3-二氢-2H-吲哚-2-酮

DATABASE IDS

MDL Number MFCD00456999
CAS Number 20870-79-5
PubChem SID 24883978

PROPERTIES

Empirical Formula (Hill Notation) C8H6N2O3
Purity 97%
Melting Point 233-236 °C
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H315-H317-H319-H335
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Faceshields, Gloves
GHS Precautionary statements P261-P280-P305 + P351 + P338
Risk Statements 36/37/38-43
Safety Statements 26-36/37
German water hazard class 3

DETAILS

Description (English)
Packaging
1, 5 g in glass bottle
Application

• Reactant for synthesis of 3-[4-(amino/methylsulfonyl)phenyl]methylene-indolin-2-one derivatives as novel COX-1/2 and 5-LOX inhibitors1
• Reactant for preparation of Aurora kinase inhibitors2
• Reactant for synthesis of 3-substituted 2-indolinone RET inhibitors3
• Reactant for synthesis of 4-azachromeno[2,3-b]indol-11(6H)-ones and derivatives as analogs of ellipticine4
• Reactant for preparation of [18F]fluorobenzylidene-indolinone as possible tyrosine kinase inhibitor for PET tumor imaging5
• Reactant for preparation of 3-substituted indolin-2-ones as neuroprotective and toxic agents6
Description (简体中文)
包装
1, 5 g in glass bottle
Application

• Reactant for synthesis of 3-[4-(amino/methylsulfonyl)phenyl]methylene-indolin-2-one derivatives as novel COX-1/2 and 5-LOX inhibitors1
• Reactant for preparation of Aurora kinase inhibitors2
• Reactant for synthesis of 3-substituted 2-indolinone RET inhibitors3
• Reactant for synthesis of 4-azachromeno[2,3-b]indol-11(6H)-ones and derivatives as analogs of ellipticine4
• Reactant for preparation of [18F]fluorobenzylidene-indolinone as possible tyrosine kinase inhibitor for PET tumor imaging5
• Reactant for preparation of 3-substituted indolin-2-ones as neuroprotective and toxic agents6

REFERENCES