7-Methoxyindole

• Catalog No.: 113980
• CAS Number: 3189-22-8
• M. F.: C9H9NO
• M. W.: 147.17386
• Purity: 97%

SYNONYMS

• Title: 7-甲氧基吲哚
• IUPAC name: 7-methoxy-1H-indole
• IUPAC Traditional name: 7-methoxy-1H-indole
• Synonyms: NSC 100739

DATABASE IDS

• MDL Number: MFCD00047203
• CAS Number: 3189-22-8
• PubChem SID: 24847155
• EC Number: 221-690-1

PROPERTIES

• Empirical Formula (Hill Notation): C9H9NO
• Purity: 97%
• Boiling Point: 108-110 °C/0.3 mmHg(lit.)
• Density: 1.126 g/mL at 25 °C(lit.)
• Flash Point: >113 °C
• Flash Point: >235.4 °F
• Refractive Index: n20/D 1.612(lit.)
• GHS Signal Word: Danger
• GHS Hazard statements: H302-H315-H318-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: 22-37/38-41
• Safety Statements: 26-39
• German water hazard class: 3

DETAILS

Description (English)

Packaging
1 g in glass bottle
Application

• Reactant for preparation of tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles as potential anticancer immunomodulators1
• Reactant for preparation of indolylindazoles and indolylpyrazolopyridines as interleukin-2 inducible T cell kinase inhibitors2
• Reactant for preparation of benzoylpiperazinyl-indolyl ethane dione derivatives as HIV-1 inhibitors3
• Reactant for preparation of bis(indolyl)alkanehydroxamic acids as histone deacetylase inhibitors4
• Reactant for preparation of β-carboline-1-carboxylic acids as inhibitors of mitogen activated protein kinase-activated protein kinase 25

Description (简体中文)

包装
1 g in glass bottle
Application

• Reactant for preparation of tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles as potential anticancer immunomodulators1
• Reactant for preparation of indolylindazoles and indolylpyrazolopyridines as interleukin-2 inducible T cell kinase inhibitors2
• Reactant for preparation of benzoylpiperazinyl-indolyl ethane dione derivatives as HIV-1 inhibitors3
• Reactant for preparation of bis(indolyl)alkanehydroxamic acids as histone deacetylase inhibitors4
• Reactant for preparation of β-carboline-1-carboxylic acids as inhibitors of mitogen activated protein kinase-activated protein kinase 25