Substance

ID:335156

Names and Identifiers
IUPAC name
2-(5-methoxy-1H-indol-3-yl)ethan-1-amine
IUPAC Traditional name
5 methoxytryptamine
Synonyms
5-Methoxyindole-3-ethanamineNSC 564225-甲氧基色胺5-MOT5-MethoxytryptamineDeacetylmelatonin2-(5-Methoxyindol-3-yl)ethylamine3-(2-Aminoethyl)-5-methoxyindole
Registration numbers
CAS Number
MDL Number
EC Number
PubChem SID
Beilstein Number
Properties
Product Information
Purity
97%
Empirical Formula (Hill Notation)
C11H14N2O
Physical Property
Melting Point
121-123 °C(lit.)
Safety Information
German water hazard class
3
GHS Hazard statements
H302
RTECS
NL4059000
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Safety Statements
36
GHS Pictograms
GHS07
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
MSDS Link
GHS Signal Word
Warning
European Hazard Symbols
Harmful Harmful (Xn)
Risk Statements
22
Pharmacology Properties
Gene Information
human ... HTR1A(3350), HTR2A(3356), HTR2C(3358)rat ... Htr2a(29595), Htr2c(25187), Htr7(65032)
Molecule Details
Packaging
1 g in glass bottle
100 mg in glass bottle
Application
Reactant for preparation of:
• Carboline disaccharide domain of shishijimicin A1
• Melatonin analogs for the reduction of intraocular pressure2
• 5-HT4 receptor ligands3
• inhibitors of sortase A and isocitrate lyase4
• Therapeutic agents for treatment of ischemia/reperfusion (I/R) injury5
• Aurora and epidermal growth factor receptor kinase inhibitors6
• Agents for the treatment of human papillomavirus infection7
• Manzamine analogues for the control of neuroinflammation and cerebral infections8
• Inhibitors of pro-inflammatory cytokines9
• Tacrine-melatonin hybrids as multifunctional agents for alzheimer′s disease10
Molecular Spectra
No Data Available
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References
No Data Available
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