Basic Information | Post buying leads | Suppliers | Cas Database |
Name |
5-FLUOROTRYPTAMINE |
EINECS | N/A |
CAS No. | 576-16-9 | Density | 1.25 g/cm3 |
PSA | 41.81000 | LogP | 2.50850 |
Solubility | N/A | Melting Point |
273-275 °C |
Formula | C10H11FN2 | Boiling Point | 345.959 °C at 760 mmHg |
Molecular Weight | 178.209 | Flash Point | 163.03 °C |
Transport Information | N/A | Appearance | N/A |
Safety | 26-36 | Risk Codes | 20/21/22-36/37/38 |
Molecular Structure | Hazard Symbols | Xn, Xi | |
Synonyms |
Indole,3-(2-aminoethyl)-5-fluoro- (6CI,7CI,8CI);2-(5-Fluoro-1H-indol-3-yl)ethylamine;2-(5-Fluoroindol-3-yl)ethylamine; |
Article Data | 21 |
5-fluoro-3-(2-nitrovinyl)indole
5-fluorotryptamine
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In tetrahydrofuran at 0 - 20℃; for 40h; | 92% |
With lithium aluminium tetrahydride In tetrahydrofuran Reflux; |
(Ε)-5-fluoro-3-(2-nitroethenyl)-1Η-indole
5-fluorotryptamine
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In tetrahydrofuran at 0 - 20℃; Inert atmosphere; | 76% |
With lithium aluminium tetrahydride In tetrahydrofuran for 5h; Ambient temperature; | |
With lithium aluminium tetrahydride In tetrahydrofuran at 20℃; for 5h; |
Conditions | Yield |
---|---|
With pyridoxal 5'-phosphate; aromatic L-amino acid decarboxylase In various solvent(s) at 30℃; for 48h; | 41% |
With NH4OH-NH4Cl buffer; pyridoxal 5'-phosphate at 30℃; for 0.5h; relative rate of CO2 evolution by aromatic L-amino acid decarboxylase from Micrococcus percitreus; |
5-fluorotryptamine
Conditions | Yield |
---|---|
Stage #1: 5-fluoro-3-(2-nitroethyl)-1Η-indole With ammonium chloride In tetrahydrofuran; ethanol at 85℃; for 0.166667h; Stage #2: With iron | 26.2% |
Conditions | Yield |
---|---|
With hydrogenchloride |
4-aminobutyrylaldehyde diethylacetal
4-fluorophenylhydrazine
5-fluorotryptamine
Conditions | Yield |
---|---|
With zinc(II) chloride at 180℃; |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1.1: POCl3 / 0.25 h / 20 °C 1.2: CaCO3 / 1,2-dichloro-ethane / 0.5 h / Heating 2.1: 60 percent / ammonium acetate / 1.5 h / Heating 3.1: LiAlH4 / tetrahydrofuran / 5 h / 20 °C View Scheme | |
Multi-step reaction with 3 steps 1: 1.) POCl3, 2.) CaCO3 / 1.) RT, 15 min, 2.) 1,2-dichloroethane, reflux, 30 min 2: 60 percent / ammonium acetate / 1.5 h / Heating 3: LiAlH4 / tetrahydrofuran / 5 h / Ambient temperature View Scheme | |
Multi-step reaction with 3 steps 1.1: trichlorophosphate / 1.25 h / 0 - 38 °C 1.2: 0.08 h / 170 °C 2.1: ammonium acetate / 1.5 h / Reflux 3.1: lithium aluminium tetrahydride / tetrahydrofuran / 40 h / 0 - 20 °C View Scheme | |
Multi-step reaction with 4 steps 1: diethyl ether / 3 h / 0 - 20 °C 2: diethyl ether / 1 h / 20 °C 3: ammonia / water / 24 h / 20 °C 4: lithium aluminium tetrahydride / tetrahydrofuran / 10 h / Reflux View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 60 percent / ammonium acetate / 1.5 h / Heating 2: LiAlH4 / tetrahydrofuran / 5 h / 20 °C View Scheme | |
Multi-step reaction with 2 steps 1: 60 percent / ammonium acetate / 1.5 h / Heating 2: LiAlH4 / tetrahydrofuran / 5 h / Ambient temperature View Scheme | |
Multi-step reaction with 2 steps 1: piperidine; acetic acid / benzene / Reflux 2: lithium aluminium tetrahydride / tetrahydrofuran / Reflux View Scheme | |
Multi-step reaction with 2 steps 1: ammonium acetate / 1.5 h / Reflux 2: lithium aluminium tetrahydride / tetrahydrofuran / 40 h / 0 - 20 °C View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: aqueous HCl; acetic acid 2: aq.-ethanolic KOH 3: aqueous HCl View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: aq.-ethanolic KOH 2: aqueous HCl View Scheme |