Substance
ID:330824
Names and Identifiers
IUPAC Traditional name
6-methyl-1H-indole
IUPAC name
6-methyl-1H-indole
Synonyms
6-甲基吲哚6-Methylindole
Registration numbers
CAS Number
PubChem SID
Beilstein Number
MDL Number
Properties
Physical Property
Density
1.059 g/mL at 25 °C(lit.)
Flash Point
230 °F
110 °C
Refractive Index
n20/D 1.607(lit.)
Boiling Point
112 °C/5 mmHg(lit.)
Safety Information
MSDS Link
Risk Statements
36/37/38
GHS Signal Word
Warning
German water hazard class
3
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
GHS Hazard statements
H315-H319-H335
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Safety Statements
26-36
European Hazard Symbols
Irritant (Xi)GHS Precautionary statements
P261-P305+P351+P338
Product Information
Purity
97%
Empirical Formula (Hill Notation)
C9H9N
Molecule Details
Packaging
1 g in glass bottle
250 mg in glass bottle
Application
• Reactant for preparation of tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles as potential anticancer immunomodulators1
• Reactant for preparation of indole linked triazole derivatives as antifungal agents2
• Reactant for preparation of N-β-D-xylosyl-indole derivatives as SGLT2 inhibitors for management of hyperglycemia in diabetes3
• Reactant for preparation of aminoguanidine derivatives of arylsulfonylacylindoles as antifungal agents4
• Reactant for preparation of indolylindazoles and indolylpyrazolopyridines as interleukin-2 inducible T cell kinase inhibitors5
• Reactant for preparation of arylsulfonylacetylindoles as anti-HIV-1 agents6
1 g in glass bottle
250 mg in glass bottle
Application
• Reactant for preparation of tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles as potential anticancer immunomodulators1
• Reactant for preparation of indole linked triazole derivatives as antifungal agents2
• Reactant for preparation of N-β-D-xylosyl-indole derivatives as SGLT2 inhibitors for management of hyperglycemia in diabetes3
• Reactant for preparation of aminoguanidine derivatives of arylsulfonylacylindoles as antifungal agents4
• Reactant for preparation of indolylindazoles and indolylpyrazolopyridines as interleukin-2 inducible T cell kinase inhibitors5
• Reactant for preparation of arylsulfonylacetylindoles as anti-HIV-1 agents6
Molecular Spectra
No Data Available
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References
No Data Available
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