3-Cyanoindole

• Catalog No.: 347949
• CAS Number: 5457-28-3
• M. F.: C9H6N2
• M. W.: 142.15734
• Purity: 98%

SYNONYMS

• Title: 3-氰基吲哚
• IUPAC name: 1H-indole-3-carbonitrile
• IUPAC Traditional name: 3-cyanoindole
• Synonyms: 3-Indolecarbonitrile; NSC 24935; 3-吲哚甲腈

DATABASE IDS

• PubChem SID: 24861537
• CAS Number: 5457-28-3
• MDL Number: MFCD00022717

PROPERTIES

• Empirical Formula (Hill Notation): C9H6N2
• Purity: 98%
• Melting Point: 179-182 °C(lit.)
• GHS Signal Word: Warning
• GHS Hazard statements: H302-H312-H315-H319-H332-H335
• European Hazard Symbols: Harmful (Xn)
• Personal Protective Equipment: dust mask type N95 (US), Eyeshields, Gloves
• GHS Precautionary statements: P261-P280-P305 + P351 + P338
• Risk Statements: 20/21/22-36/37/38
• Safety Statements: 26-37/39
• German water hazard class: 3

DETAILS

Description (English)

Packaging
1, 5 g in glass bottle
Application
Reactant for preparation of:
• Tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles as potential anticancer immunomodulators1
• Inhibitors of the C-terminal domain of RNA polymerase II with antitumor activities
• 4-substituted β-lactams2
• Biologically active Indoles3
• Inhibitors of glycogen synthase kinase 3β (GSK-3)4
• HIV-1 integrase inhibitors5
• Indole fragments as inosine monophosphate dehydrogenase (IMPDH) inhibitors6
• Aziridinomitosene skeleton7
• Potential antiviral agents8Reactant for:
• Intramolecular oxidative C-H coupling reactions with applications in medium-ring synthesis techniques9

Description (简体中文)

包装
1, 5 g in glass bottle
Application
Reactant for preparation of:
• Tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles as potential anticancer immunomodulators1
• Inhibitors of the C-terminal domain of RNA polymerase II with antitumor activities
• 4-substituted β-lactams2
• Biologically active Indoles3
• Inhibitors of glycogen synthase kinase 3β (GSK-3)4
• HIV-1 integrase inhibitors5
• Indole fragments as inosine monophosphate dehydrogenase (IMPDH) inhibitors6
• Aziridinomitosene skeleton7
• Potential antiviral agents8Reactant for:
• Intramolecular oxidative C-H coupling reactions with applications in medium-ring synthesis techniques9