DayangChem exported this product to many countries and regions at best price. If you are looking for the material's manufacturer or supplier in China, DayangChem is your best choice. Pls contact with us freely for getting detailed product spe
Cas:14490-05-2
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inquiryhigh purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:drum and bag Application:for pharma use Transportation:by sea or air Port:Beijing or Guangzhou
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inquiry7-Methyltryptamine cas 14490-05-2Appearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express
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inquiryhigh purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:Foil bag; Drum; Plastic bottle Application:Pharma;Industry;Agricultural Transportation:by sea or air Port:any port in China
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FINETECH INDUSTRY LIMITED is a LONDON based CRO company providing drug discovery & development services to worldwide clients. FINETECH INDUSTRY LIMITED supplies the 7-Methyltryptamine, CAS:14490-05-2 with the most competitive price and the best quali
2-(7-Methyl-1H-indol-3-yl)ethanamine Application:2050393
Cas:14490-05-2
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inquiry7-methyltryptamine
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In tetrahydrofuran at 0 - 20℃; Inert atmosphere; | 99% |
With lithium aluminium tetrahydride In tetrahydrofuran |
2-(7-methyl-1H-indol-3-yl)acetonitrile
7-methyltryptamine
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride |
3-(2-amino-ethyl)-7-methyl-indole-2-carboxylic acid
7-methyltryptamine
Conditions | Yield |
---|---|
With hydrogenchloride |
4-aminobutyrylaldehyde diethylacetal
2-methylphenylhydrazine
7-methyltryptamine
Conditions | Yield |
---|---|
With zinc(II) chloride |
7-methyl-1H-indole
7-methyltryptamine
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: POCl3 2: AcOH 3: LiAH4 / tetrahydrofuran View Scheme | |
Multi-step reaction with 3 steps 1.1: trichlorophosphate / 1.5 h / Cooling with ice 1.2: 20 °C / Cooling with ice 1.3: 1 h / 105 °C 2.1: ammonium acetate / Reflux 3.1: lithium aluminium tetrahydride / tetrahydrofuran / 0 - 20 °C / Inert atmosphere View Scheme | |
Multi-step reaction with 3 steps 1: diethyl ether / 18 h / 40 °C 2: ammonia / 1,4-dioxane / 20 °C 3: lithium aluminium tetrahydride / tetrahydrofuran / 18 h / Reflux View Scheme | |
Multi-step reaction with 3 steps 1.1: trichlorophosphate / 0.25 h / 0 °C / Inert atmosphere 1.2: 3.25 h / 0 - 20 °C / Inert atmosphere 1.3: 0.08 h / Reflux 2.1: ammonium acetate / 1.5 h / Reflux; Inert atmosphere 3.1: lithium aluminium tetrahydride / tetrahydrofuran / 36 h / 0 - 20 °C / Inert atmosphere View Scheme |
7-methyl-1H-indole-3-carbaldehyde
7-methyltryptamine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: AcOH 2: LiAH4 / tetrahydrofuran View Scheme | |
Multi-step reaction with 2 steps 1: ammonium acetate / Reflux 2: lithium aluminium tetrahydride / tetrahydrofuran / 0 - 20 °C / Inert atmosphere View Scheme | |
Multi-step reaction with 2 steps 1: ammonium acetate / 2 h / Reflux 2: lithium aluminium tetrahydride / tetrahydrofuran / 36 h / 0 - 20 °C / Inert atmosphere View Scheme | |
Multi-step reaction with 2 steps 1: ammonium acetate / 1.5 h / Reflux; Inert atmosphere 2: lithium aluminium tetrahydride / tetrahydrofuran / 36 h / 0 - 20 °C / Inert atmosphere View Scheme |
8-methyl-2,3,4,9-tetrahydro-β-carbolin-1-one
7-methyltryptamine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: aq.-ethanolic KOH 2: aqueous HCl View Scheme |
1-methyl-2-nitrobenzene
7-methyltryptamine
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1.1: tetrahydrofuran / 1 h / -40 °C / Inert atmosphere 2.1: trichlorophosphate / 1.5 h / Cooling with ice 2.2: 20 °C / Cooling with ice 2.3: 1 h / 105 °C 3.1: ammonium acetate / Reflux 4.1: lithium aluminium tetrahydride / tetrahydrofuran / 0 - 20 °C / Inert atmosphere View Scheme |
2-(7-methyl-1H-indol-3-yl)-2-oxoacetyl chloride
7-methyltryptamine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: ammonia / 1,4-dioxane / 20 °C 2: lithium aluminium tetrahydride / tetrahydrofuran / 18 h / Reflux View Scheme |
7-methyltryptamine
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In tetrahydrofuran for 18h; Reflux; |
C11H10N2O2
7-methyltryptamine
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In tetrahydrofuran at 0 - 20℃; for 36h; Inert atmosphere; | |
With lithium aluminium tetrahydride In tetrahydrofuran at 0 - 20℃; for 36h; Inert atmosphere; |
7-methyltryptamine
3-oxo-pyrrolidine-1-carboxylic acid tert-butyl ester
Conditions | Yield |
---|---|
Stage #1: 7-methyltryptamine; 3-oxo-pyrrolidine-1-carboxylic acid tert-butyl ester With acetic acid at 100℃; for 4.5h; Stage #2: With hydrogenchloride In 1,2-dioxacyclohexane at 20℃; | 100% |
7-methyltryptamine
7-(trifluoromethyl)-3,4,5,6-tetrahydro-2H-azepine
Conditions | Yield |
---|---|
With trifluoroacetic acid In dichloromethane at 20℃; for 168h; Pictet-Spengler Synthesis; | 100% |
7-methyltryptamine
acetic anhydride
N-(2-(7-methyl-1H-indol-3-yl)ethyl)acetamide
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran at 20℃; for 1h; | 99% |
Conditions | Yield |
---|---|
In dimethyl sulfoxide at 80℃; for 5h; | 99% |
7-methyltryptamine
hept-3-ynoic acid
(11bR)-10-methyl-11b-n-propyl-1,2,5,6,11,11b-hexahydro-3H-indolizino[8,7-b]indol-3-one
Conditions | Yield |
---|---|
Stage #1: hept-3-ynoic acid With triphenylphosphine gold (I) chloride; silver trifluoromethanesulfonate In toluene at 20℃; for 1h; Stage #2: 7-methyltryptamine With (R)-3,3'-bis(triphenylsilyl)-1,1'-binaphthyl-2,2'-diyl hydrogenphosphate In toluene at 80 - 110℃; for 48h; optical yield given as %ee; enantioselective reaction; | 96% |
7-methyltryptamine
(11bS)-10-methyl-11b-phenyl-1,2,5,6,11,11b-hexahydro-3H-indolizino[8,7-b]indol-3-one
Conditions | Yield |
---|---|
With (R)-3,3'-bis(triphenylsilyl)-1,1'-binaphthyl-2,2'-diyl hydrogenphosphate In toluene at 110℃; for 41h; optical yield given as %ee; enantioselective reaction; | 95% |
7-methyltryptamine
3-methyllevulinic acid
(1R,11bR)-1,10,11b-trimethyl-1,2,5,6,11,11b-hexahydro-3H-indolizino[8,7-b]indol-3-one
Conditions | Yield |
---|---|
With (R)-3,3'-bis(triphenylsilyl)-1,1'-binaphthyl-2,2'-diyl hydrogenphosphate In toluene for 48h; Reflux; optical yield given as %ee; enantioselective reaction; | 95% |
7-methyltryptamine
benzaldehyde
8-methyl-1-phenyl-2,3,4,9-tetrahydro-1H-β-carboline
Conditions | Yield |
---|---|
With 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide In ethyl acetate at 110℃; for 0.166667h; Microwave irradiation; Sealed tube; | 95% |
7-methyltryptamine
N-[2-(7-methyl-1H-indol-3-yl)ethyl]but-3-yne-1-sulfonamide
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at -78℃; Inert atmosphere; | 95% |
7-methyltryptamine
di-tert-butyl dicarbonate
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran at 20℃; | 95% |
7-methyltryptamine
(+/-)-3-acetylheptanoic acid
(1R,11bR)-1-butyl-10,11b-dimethyl-1,2,5,6,11,11b-hexahydro-3H-indolizino[8,7-b]indol-3-one
Conditions | Yield |
---|---|
With (R)-3,3'-bis-(triphenylsilyl)octahydrobinolphosphoric acid In toluene for 72h; Reflux; optical yield given as %ee; enantioselective reaction; | 94% |
7-methyltryptamine
cinnamyl methyl carbonate
N-(2-(7-methyl-1H-indol-3-yl)ethyl)-1-phenylprop-2-en-1-amine
Conditions | Yield |
---|---|
With C48H49IrNO2P(1+)*CF3O3S(1-) In tetrahydrofuran at 50℃; Schlenk technique; Inert atmosphere; | 94% |
5-methyl-2-furanone
7-methyltryptamine
(11bR)-10,11b-dimethyl-1,2,5,6,11,11b-hexahydro-3H-indolizino[8,7-b]indol-3-one
Conditions | Yield |
---|---|
With (R)-3,3'-bis(triphenylsilyl)-1,1'-binaphthyl-2,2'-diyl hydrogenphosphate In toluene at 110℃; for 24h; optical yield given as %ee; enantioselective reaction; | 92% |
7-methyltryptamine
2-oxocycloheptaneacetic acid
(5aR,15bR)-14-methyl-2,3,4,5,5a,6,10,15-octahydro-9H-cyclohepta[1,8a]indolizino[8,7-b]indol-7(1H)-one
Conditions | Yield |
---|---|
With (R)-3,3'-bis-(triphenylsilyl)octahydrobinolphosphoric acid In toluene for 48h; Reflux; optical yield given as %ee; enantioselective reaction; | 91% |
7-methyltryptamine
ethyl 2-(2-oxocyclohexyl)acetate
(4aR,14bR)-13-methyl-1,2,3,4,4a,5,9,14-octahydro-6H,8H-pyrido[3,4-b:1,2-i']diindol-6-one
Conditions | Yield |
---|---|
With (R)-3,3'-bis-(triphenylsilyl)octahydrobinolphosphoric acid In toluene for 48h; Reflux; optical yield given as %ee; enantioselective reaction; | 89% |
7-methyltryptamine
p-bromophenylpropene methyl carbonate
1-(4-bromophenyl)-N-(2-(7-methyl-1H-indol-3-yl)ethyl)prop-2-en-1-amine
Conditions | Yield |
---|---|
With C48H49IrNO2P(1+)*CF3O3S(1-) In tetrahydrofuran at 50℃; Schlenk technique; Inert atmosphere; | 87% |
7-methyltryptamine
N-(2-(7-methyl-1H-indol-3-yl)ethyl)-1-(3-(trifluoromethyl)phenyl)prop-2-en-1-amine
Conditions | Yield |
---|---|
With C48H49IrNO2P(1+)*CF3O3S(1-) In tetrahydrofuran at 50℃; Schlenk technique; Inert atmosphere; | 86% |
7-methyltryptamine
N-ethoxycarbonylphthalimide
2-[2-(7-Methyl-1H-indol-3-yl)-ethyl]-isoindole-1,3-dione
Conditions | Yield |
---|---|
In tetrahydrofuran for 48h; Heating; | 85% |
7-methyltryptamine
dec-3-ynoic acid
(11bR)-11b-hexyl-10-methyl-1,2,5,6,11,11b-hexahydro-3H-indolizino[8,7-b]indol-3-one
Conditions | Yield |
---|---|
Stage #1: dec-3-ynoic acid With triphenylphosphine gold (I) chloride; silver trifluoromethanesulfonate In toluene at 20℃; for 1h; Stage #2: 7-methyltryptamine With (R)-3,3'-bis(triphenylsilyl)-1,1'-binaphthyl-2,2'-diyl hydrogenphosphate In toluene at 80 - 110℃; for 48h; optical yield given as %ee; enantioselective reaction; | 84% |
7-methyltryptamine
acetophenone
Conditions | Yield |
---|---|
With dihydrogen peroxide; iodine In water; dimethyl sulfoxide at 110℃; | 84% |
Conditions | Yield |
---|---|
In ethanol at 60℃; for 18h; | 82% |
7-methyltryptamine
methyl chloroformate
Conditions | Yield |
---|---|
With sodium hydroxide In ethyl acetate at 20℃; | 82% |
With triethylamine In dichloromethane at 0 - 20℃; for 3h; Inert atmosphere; | |
With sodium hydroxide In water; ethyl acetate at 20℃; for 1h; Inert atmosphere; | |
With sodium carbonate In dichloromethane; water for 2h; Inert atmosphere; |
7-methyltryptamine
hexadec-3-ynoic acid
(11bR)-11b-dodecyl-10-methyl-1,2,5,6,11,11b-hexahydro-3H-indolizino[8,7-b]indol-3-one
Conditions | Yield |
---|---|
Stage #1: hexadec-3-ynoic acid With triphenylphosphine gold (I) chloride; silver trifluoromethanesulfonate In toluene at 20℃; for 1h; Stage #2: 7-methyltryptamine With (R)-3,3'-bis(triphenylsilyl)-1,1'-binaphthyl-2,2'-diyl hydrogenphosphate In toluene at 80 - 110℃; for 48h; optical yield given as %ee; enantioselective reaction; | 81% |
7-methyltryptamine
(+/-)-3-ethyl-4-oxopentanoic acid
(1R,11bR)-1-ethyl-10,11b-dimethyl-1,2,5,6,11,11b-hexahydro-3H-indolizino[8,7-b]indol-3-one
Conditions | Yield |
---|---|
With (R)-3,3'-bis-(triphenylsilyl)octahydrobinolphosphoric acid In toluene for 54h; Reflux; optical yield given as %ee; enantioselective reaction; | 81% |
7-methyltryptamine
1-(4-isobutylphenyl)-N-(2-(7-methyl-1H-indol-3-yl)ethyl)prop-2-en-1-amine
Conditions | Yield |
---|---|
With C48H49IrNO2P(1+)*CF3O3S(1-) In tetrahydrofuran at 50℃; Schlenk technique; Inert atmosphere; | 78% |
7-methyltryptamine
N-(2-(7-methyl-1H-indol-3-yl)ethyl)but-3-en-2-amine
Conditions | Yield |
---|---|
With C48H49IrNO2P(1+)*CF3O3S(1-) In tetrahydrofuran at 50℃; Schlenk technique; Inert atmosphere; | 78% |
7-methyltryptamine
hept-1-en-3-yl methyl carbonate
N-(2-(7-methyl-1H-indol-3-yl)ethyl)hept-1-en-3-amine
Conditions | Yield |
---|---|
With C48H49IrNO2P(1+)*CF3O3S(1-) In tetrahydrofuran at 50℃; Schlenk technique; Inert atmosphere; | 78% |
7-methyltryptamine
6-(trifluoromethyl)-2,3,4,5-tetrahydropyridine
Conditions | Yield |
---|---|
With camphor-10-sulfonic acid In water at 130℃; for 14h; Pictet-Spengler Synthesis; | 77% |
7-methyltryptamine
3,6-dibromo-9-(oxiran-2-ylmethyl)-9H-carbazole
Conditions | Yield |
---|---|
In ethanol for 12h; Inert atmosphere; Reflux; | 77% |
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