Indole-5-carbonitrile

• Catalog No.: C92006
• CAS Number: 15861-24-2
• M. F.: C9H6N2
• M. W.: 142.15734
• Purity: 99%

SYNONYMS

• Title: 吲哚-5-甲腈
• IUPAC name: 1H-indole-5-carbonitrile
• IUPAC Traditional name: indole-5-cyano-
• Synonyms: 5-Cyanoindole

DATABASE IDS

• CAS Number: 15861-24-2
• PubChem SID: 24893140
• EC Number: 239-986-4
• MDL Number: MFCD00005669
• Beilstein Number: 116738

PROPERTIES

• Empirical Formula (Hill Notation): C9H6N2
• Purity: 99%
• Melting Point: 106-108 °C(lit.)
• GHS Signal Word: Warning
• GHS Hazard statements: H315-H319-H335
• European Hazard Symbols: Irritant (Xi)
• Personal Protective Equipment: dust mask type N95 (US), Eyeshields, Gloves
• GHS Precautionary statements: P261-P305 + P351 + P338
• Risk Statements: 36/37/38
• RTECS: NL5993120
• Safety Statements: 26-36
• German water hazard class: 3

DETAILS

Description (English)

Packaging
5, 10 g in glass bottle
Application

• Reactant for parallel synthesis of dihydroisoquinolines via silver and L-proline co-catalyzed three-component coupling reaction1
• Reactant for chemoselective and regioselective preparation of benzoyl indoles2
• Reactant for preparation of novel PPARα/γ dual agonists for potential treatment of metabolic syndrome and IDDM3
• Reactant for preparation of 4,5-dihydrocyclopenta[c]quinolines by palladium-catalyzed ring-expansion reaction alkynes, using O2 as the oxidant4
• Reactant for preparation of vinylindoles by hydroarylation of alkynes using indium bromide catalyst5
• Reactant for gold catalyzed direct alkynylation using a benziodoxolone based hypervalent iodine reagent6

Description (简体中文)

包装
5, 10 g in glass bottle
Application

• Reactant for parallel synthesis of dihydroisoquinolines via silver and L-proline co-catalyzed three-component coupling reaction1
• Reactant for chemoselective and regioselective preparation of benzoyl indoles2
• Reactant for preparation of novel PPARα/γ dual agonists for potential treatment of metabolic syndrome and IDDM3
• Reactant for preparation of 4,5-dihydrocyclopenta[c]quinolines by palladium-catalyzed ring-expansion reaction alkynes, using O2 as the oxidant4
• Reactant for preparation of vinylindoles by hydroarylation of alkynes using indium bromide catalyst5
• Reactant for gold catalyzed direct alkynylation using a benziodoxolone based hypervalent iodine reagent6