3-Formyl-1H-indole-5-carbonitrile

• Catalog No.: 701327
• CAS Number: 17380-18-6
• M. F.: C10H6N2O
• M. W.: 170.16744
• Purity: 97%

SYNONYMS

• Title: 5-氰基吲哚-3-甲醛
• IUPAC name: 3-formyl-1H-indole-5-carbonitrile
• IUPAC Traditional name: 3-formyl-1H-indole-5-carbonitrile
• Synonyms: 3-甲酰-5-氰基-1H-吲哚; 5-Cyanoindole-3-carboxaldehyde; 3-Formyl-5-cyano-1H-indole

DATABASE IDS

• CAS Number: 17380-18-6
• MDL Number: MFCD01719101

PROPERTIES

• Empirical Formula (Hill Notation): C10H6N2O
• Purity: 97%
• Melting Point: 248-253 °C
• GHS Signal Word: Warning
• GHS Hazard statements: H302-H312-H315-H317-H319-H332-H335
• European Hazard Symbols: Harmful (Xn)
• Personal Protective Equipment: dust mask type N95 (US), Eyeshields, Faceshields, Gloves
• GHS Precautionary statements: P261-P280-P305 + P351 + P338
• Risk Statements: 20/21/22-36/37/38-43
• 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 tryptophan dioxygenase inhibitors as potential anticancer immunomodulators1
• Reactant for enantioselective preparation of antifungal agents2
• Reactant for synthesis of indole- and 7-azaindole-1,3-dicarboxamide hydroxyethylamine inhibitors of BACE-13
• Reactant for preparation of indolyl alkenes from microwave-enhanced Knoevenagel condensation as antibacterial agents4
• Reactant for preparation of indolecarboxamide derivatives as antitumor agents5
• Reactant for synthesis of a selective serotonin reuptake inhibitor6

Description (简体中文)

包装
1, 5 g in glass bottle
Application

• Reactant for synthesis of tryptophan dioxygenase inhibitors as potential anticancer immunomodulators1
• Reactant for enantioselective preparation of antifungal agents2
• Reactant for synthesis of indole- and 7-azaindole-1,3-dicarboxamide hydroxyethylamine inhibitors of BACE-13
• Reactant for preparation of indolyl alkenes from microwave-enhanced Knoevenagel condensation as antibacterial agents4
• Reactant for preparation of indolecarboxamide derivatives as antitumor agents5
• Reactant for synthesis of a selective serotonin reuptake inhibitor6