4-Cyanoindole

• Catalog No.: 645532
• CAS Number: 16136-52-0
• M. F.: C9H6N2
• M. W.: 142.15734
• Purity: 97%

SYNONYMS

• Title: 4-氰基吲哚
• IUPAC name: 1H-indole-4-carbonitrile
• IUPAC Traditional name: indole-4-cyano-
• Synonyms: Indole-4-carbonitrile

DATABASE IDS

• CAS Number: 16136-52-0
• MDL Number: MFCD00152045
• PubChem SID: 24883383

PROPERTIES

• Empirical Formula (Hill Notation): C9H6N2
• Purity: 97%
• Melting Point: 117-121 °C(lit.)
• GHS Signal Word: Danger
• GHS Hazard statements: H302-H315-H317-H318-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: 22-37/38-41-43
• Safety Statements: 26-36/37/39
• German water hazard class: 3

DETAILS

Description (English)

Packaging
1, 5 g in glass bottle
Application
Reactant for preparation of tryptophan dioxygenase inhibitors as potential anticancer immunomodulators1Reactant for stereoselective preparation of γ-lactones via prolinol silyl ether catalyzed Friedel-Crafts alkylation reaction2Reactant for iridium-catalyzed borylation reactions3Reactant for parallel synthesis of N-benzylisatin oximes as JNK3 MAP kinase inhibitors4Reactant for preparation of N-aryl indoles5Reactant for preparation of conformationally restricted indole cyclopropylmethylamines as selective serotonin reuptake inhibitors6

Description (简体中文)

包装
1, 5 g in glass bottle
Application
Reactant for preparation of tryptophan dioxygenase inhibitors as potential anticancer immunomodulators1Reactant for stereoselective preparation of γ-lactones via prolinol silyl ether catalyzed Friedel-Crafts alkylation reaction2Reactant for iridium-catalyzed borylation reactions3Reactant for parallel synthesis of N-benzylisatin oximes as JNK3 MAP kinase inhibitors4Reactant for preparation of N-aryl indoles5Reactant for preparation of conformationally restricted indole cyclopropylmethylamines as selective serotonin reuptake inhibitors6