1-Methylindole-2-carboxylic acid

• Catalog No.: 134155
• CAS Number: 16136-58-6
• M. F.: C10H9NO2
• M. W.: 175.18396
• Purity: 98%

SYNONYMS

• Title: 1-甲基吲哚-2-甲酸
• IUPAC name: 1-methyl-1H-indole-2-carboxylic acid
• IUPAC Traditional name: 1-methylindole-2-carboxylic acid
• Synonyms: NSC 68357

DATABASE IDS

• CAS Number: 16136-58-6
• MDL Number: MFCD00005801
• PubChem SID: 24848134

PROPERTIES

• Empirical Formula (Hill Notation): C10H9NO2
• Purity: 98%
• Melting Point: 212-213 °C (dec.)(lit.)
• GHS Signal Word: Warning
• GHS Hazard statements: H302-H315-H319-H335
• European Hazard Symbols: Harmful (Xn)
• Personal Protective Equipment: dust mask type N95 (US), Eyeshields, Faceshields, Gloves
• GHS Precautionary statements: P261-P305 + P351 + P338
• Risk Statements: 22-36/37/38
• RTECS: NL6012400
• Safety Statements: 26
• German water hazard class: 3

DETAILS

Description (English)

Packaging
1, 5 g in glass bottle
Application

• Reactant for preparation of keto-indoles as novel indoleamine 2,3-dioxygenase (IDO) inhibitors1
• Reactant for synthesis of fenbufen and ethacrynic acid derivatives as potential antitumor agents via amide coupling reactions2
• Reactant for diastereoselective synthesis of vinylated heterocycles via ruthenium-catalyzed oxidative vinylation with alkenes3
• Reactant for synthesis of 2,3-dihalo indoles via hypervalent iodine mediated decarboxylative halogenation4
• Reactant for preparation of α-ketoamides as cathepsin S inhibitors with potential applications against tumor invasion and angiogenesis5
• Reactant for preparation of anthranilic acid mimics as bacterial translation inhibitors6

Description (简体中文)

包装
1, 5 g in glass bottle
Application

• Reactant for preparation of keto-indoles as novel indoleamine 2,3-dioxygenase (IDO) inhibitors1
• Reactant for synthesis of fenbufen and ethacrynic acid derivatives as potential antitumor agents via amide coupling reactions2
• Reactant for diastereoselective synthesis of vinylated heterocycles via ruthenium-catalyzed oxidative vinylation with alkenes3
• Reactant for synthesis of 2,3-dihalo indoles via hypervalent iodine mediated decarboxylative halogenation4
• Reactant for preparation of α-ketoamides as cathepsin S inhibitors with potential applications against tumor invasion and angiogenesis5
• Reactant for preparation of anthranilic acid mimics as bacterial translation inhibitors6