N-Acetyl-2-oxindole

• Catalog No.: 563978
• CAS Number: 21905-78-2
• M. F.: C10H9NO2
• M. W.: 175.18396
• Purity: 97%

SYNONYMS

• Title: N-乙酰基-2-羟基吲哚
• IUPAC name: 1-acetyl-2,3-dihydro-1H-indol-2-one
• IUPAC Traditional name: 1-acetyl-3H-indol-2-one
• Synonyms: N-乙酰基吲哚酮; N-Acetyloxindole; 1-Acetyl-1,3-dihydro-indol-2-one; NSC 286428

DATABASE IDS

• PubChem SID: 24880143
• MDL Number: MFCD00187672
• CAS Number: 21905-78-2

PROPERTIES

• Empirical Formula (Hill Notation): C10H9NO2
• Purity: 97%
• Melting Point: 127-131 °C(lit.)
• Personal Protective Equipment: Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
• German water hazard class: 3

DETAILS

Description (English)

Packaging
5, 25 g in glass bottle
Application

• Reactant for preparation of 4-azachromeno[2,3-b]indol-11(6H)-ones and derivatives as analogs of ellipticine1
• Reactant for preparation of indolopyrrolopyrans by solid-supported microwave-accelerated tandem intramolecular Knoevenagel/hetero Diels-Alder reaction2
• Reactant for synthesis of phytoalexins and analogs via Vilsmeier formylation-amination as antifungal agents3

Description (简体中文)

包装
5, 25 g in glass bottle
Application

• Reactant for preparation of 4-azachromeno[2,3-b]indol-11(6H)-ones and derivatives as analogs of ellipticine1
• Reactant for preparation of indolopyrrolopyrans by solid-supported microwave-accelerated tandem intramolecular Knoevenagel/hetero Diels-Alder reaction2
• Reactant for synthesis of phytoalexins and analogs via Vilsmeier formylation-amination as antifungal agents3