1-Methyl-3-indoleacetic acid

• Catalog No.: 465321
• CAS Number: 1912-48-7
• M. F.: C11H11NO2
• M. W.: 189.21054
• Purity: 98%

SYNONYMS

• Title: 1-甲基-3-吲哚乙酸
• IUPAC name: 2-(1-methyl-1H-indol-3-yl)acetic acid
• IUPAC Traditional name: (1-methylindol-3-yl)acetic acid
• Synonyms: NSC 78007; 2-(N-Methylindole-3-yl)acetic acid

DATABASE IDS

• MDL Number: MFCD00130160
• CAS Number: 1912-48-7
• PubChem SID: 24870268

PROPERTIES

• Empirical Formula (Hill Notation): C11H11NO2
• Purity: 98%
• Melting Point: 126-128 °C(lit.)
• GHS Signal Word: Danger
• GHS Hazard statements: H302-H315-H318-H335
• European Hazard Symbols: Harmful (Xn)
• GHS Precautionary statements: P261-P280-P305 + P351 + P338
• Risk Statements: 22-37/38-41
• Safety Statements: 26-39
• German water hazard class: 3

DETAILS

Description (English)

Packaging
5 g in glass bottle
Application

• Reactant for enantioselective preparation of α-aryl alkylcarboxylic acids1
• Reactant for preparation of PKC inhibitor methylindolylpyridinylmethylpiperidinylindolylpyrroledione for protein kinase C imaging2
• Reactant for stereoselective preparation of δ-lactones via Michael addition/lactonization with unsaturated carboxylates3
• Reactant for stereoselective preparation of vindorosine, vindoline, and analogs4
• Reactant for preparation of (indolyl)pyrrol-2-ones as VEGF-R inhibitors, antiangiogenic agents, and protein kinase inhibitors5
• Reactant for synthesis of 3-aryl-5-alkyl-2,5-dihydrofuran-2-ones and their carbanalogues as antifungal agents6

Description (简体中文)

包装
5 g in glass bottle
Application

• Reactant for enantioselective preparation of α-aryl alkylcarboxylic acids1
• Reactant for preparation of PKC inhibitor methylindolylpyridinylmethylpiperidinylindolylpyrroledione for protein kinase C imaging2
• Reactant for stereoselective preparation of δ-lactones via Michael addition/lactonization with unsaturated carboxylates3
• Reactant for stereoselective preparation of vindorosine, vindoline, and analogs4
• Reactant for preparation of (indolyl)pyrrol-2-ones as VEGF-R inhibitors, antiangiogenic agents, and protein kinase inhibitors5
• Reactant for synthesis of 3-aryl-5-alkyl-2,5-dihydrofuran-2-ones and their carbanalogues as antifungal agents6