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Cas:1125-60-6
Min.Order:1 Metric Ton
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Type:Manufacturers
inquiryFactory supply 5-Aminoisoquinoline CAS 1125-60-6 with good quality Company profile Wuhan Fortuna Chemical Co.,Ltd established in 2006, is a big integrative chemical enterprise being engaged in Pharmaceutical & its intermediates, Food/Feed ad
Cas:1125-60-6
Min.Order:10 Kilogram
FOB Price: $10.0
Type:Trading Company
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Cas:1125-60-6
Min.Order:1 Kilogram
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Type:Lab/Research institutions
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Cas:1125-60-6
Min.Order:5 Kiloliter
FOB Price: $1.2 / 5.0
Type:Manufacturers
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Cas:1125-60-6
Min.Order:1 Kilogram
FOB Price: $1.0 / 10.0
Type:Trading Company
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Cas:1125-60-6
Min.Order:1 Kilogram
FOB Price: $139.0 / 210.0
Type:Trading Company
inquiryAppearance:yellow to brown crystalline powder Storage:R T Package:25kg/Barrel Application:Chemicals Transportation:Express/Sea/Air Port:Any port in China
Cas:1125-60-6
Min.Order:1 Kilogram
FOB Price: $1.0
Type:Lab/Research institutions
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Cas:1125-60-6
Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
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Cas:1125-60-6
Min.Order:1 Gram
FOB Price: $1.0 / 1.2
Type:Trading Company
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Cas:1125-60-6
Min.Order:1 Gram
Negotiable
Type:Lab/Research institutions
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Cas:1125-60-6
Min.Order:1 Kilogram
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Type:Lab/Research institutions
inquiryHenan Wentao Chemical Product Co.,Ltd is Located in Zhengzhou High-tech Development Zone with import and export license, We passed ISO 9001:2008 as well, Henan Wentao has developed more than 1000 compounds, which are widely used in the fields of prod
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Cas:1125-60-6
Min.Order:10 Gram
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Type:Trading Company
inquiryHangzhou KeyingChem Co., Ltd. exported this product to many countries and regions at best price. If you are looking for the material’s manufacturer or supplier in China, KeyingChem is your best choice. Pls contact with us freely for getting det
Cas:1125-60-6
Min.Order:0 Metric Ton
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Type:Lab/Research institutions
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Cas:1125-60-6
Min.Order:10 Gram
FOB Price: $100.0
Type:Lab/Research institutions
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Our company was built in 2009 with an ISO certificate.In the past 6 years, we have grown up as a famous fine chemicals supplier in China and we had established stable business relationships with Samsung,LG,Merck,Thermo Fisher Scientific and so
Cas:1125-60-6
Min.Order:1 Metric Ton
FOB Price: $1200.0
Type:Lab/Research institutions
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Cas:1125-60-6
Min.Order:1 Kilogram
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Type:Lab/Research institutions
inquiryOur Advantages A. International Top level TechnologyOur company owned biomedicine experts are famous at home and abroad with rich experience in research and development in the field of efficient chiral functional molecules research and development an
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Cas:1125-60-6
Min.Order:1 Kilogram
FOB Price: $18.0 / 20.0
Type:Trading Company
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Cas:1125-60-6
Min.Order:1 Gram
Negotiable
Type:Lab/Research institutions
inquiry1.Applied in food field.it can improve the immune system and prolong life. 2.Appliedin cosmetic field.it can improve the skin care. 3.Applied in pharmaceutical field.it can treat various dieases. 4.Our product quality assurance will make our customer
Cas:1125-60-6
Min.Order:1 Metric Ton
FOB Price: $1.5
Type:Trading Company
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Cas:1125-60-6
Min.Order:0
Negotiable
Type:Lab/Research institutions
inquiryGOLDEN PHARMA CO.,LIMITED.is a professional pharmaceutical company,our team have more than 20years expereince in pharmaceutical production and sales. we are a professional technical enterprise specializing in the R & D, production,QA regulation
Conditions | Yield |
---|---|
With indium; ammonium chloride In ethanol for 1h; Heating; | 99% |
With palladium 10% on activated carbon; hydrogen at 20℃; for 1h; | 99% |
With indium; ammonium chloride In ethanol Heating; | 99% |
5-bromoisoquinoline
isoquinolin-5-ylamine
Conditions | Yield |
---|---|
With 2-((dicyclohexylphosphino)methyl)-1,3-bis(2,6-diisopropylphenyl)-4,5-dimethyl-1H-imidazol-3-ium iodide; ammonia; palladium diacetate; sodium t-butanolate In 1,4-dioxane at 120℃; under 7500.75 Torr; for 24h; Autoclave; Inert atmosphere; | 99% |
With lithium amide; (CyPF-t-Bu)PdCl2 In 1,2-dimethoxyethane at 90℃; for 24h; | 79% |
With ammonia; palladium diacetate; sodium t-butanolate; 2-(di-tert-butyl-phosphino)-1-phenyl-1H-pyrrole In 1,4-dioxane at 120℃; under 7500.75 Torr; for 24h; Autoclave; Inert atmosphere; | 78 %Chromat. |
5-Nitroisoquinoline N-Oxide
isoquinolin-5-ylamine
Conditions | Yield |
---|---|
With titanium(III) chloride In acetic acid at 18℃; for 0.116667h; | 97.8% |
With hydrogenchloride; palladium on activated charcoal Hydrogenation; |
5-nitroisoquinoline hydrobromide
isoquinolin-5-ylamine
Conditions | Yield |
---|---|
With titanium(III) chloride In acetic acid at 20℃; for 0.116667h; | 86.8% |
Conditions | Yield |
---|---|
Stage #1: 5-bromoisoquinoline With lithium amide; [(CyPF-tBu)PdCl2] In 1,2-dimethoxyethane at 90℃; for 24h; Sealed vial; Stage #2: With hydrogenchloride In 1,2-dimethoxyethane; water at 20℃; for 0.0833333h; Stage #3: With sodium hydrogencarbonate In 1,2-dimethoxyethane; water Product distribution / selectivity; | A 79% B n/a |
Stage #1: 5-bromoisoquinoline With ammonia; sodium t-butanolate; [(CyPF-tBu)PdCl2] In 1,2-dimethoxyethane at 90℃; under 4137.29 - 10343.2 Torr; for 20h; Stage #2: With hydrogenchloride In 1,2-dimethoxyethane; water at 20℃; for 0.0833333h; Stage #3: With sodium hydrogencarbonate In 1,2-dimethoxyethane; water Product distribution / selectivity; | A 70% B n/a |
Conditions | Yield |
---|---|
With ammonium sulfate; C39H45FeNNiP2; sodium t-butanolate In 2-methyltetrahydrofuran at 100℃; for 7h; Reagent/catalyst; Solvent; Inert atmosphere; Glovebox; Autoclave; | 75% |
Conditions | Yield |
---|---|
With sodium tetrahydroborate; 5%-palladium/activated carbon; hydrazine hydrate; lithium hydroxide In 1,4-dioxane at 170℃; for 16h; Molecular sieve; Inert atmosphere; | 30% |
With ammonium hydroxide; sulfur dioxide at 150 - 160℃; |
5-amino-1-chloroisoquinoline
isoquinolin-5-ylamine
Conditions | Yield |
---|---|
With dihydrogen hexachloroplatinate; sodium hydroxide; nickel Hydrogenation; |
5-Nitroisoquinoline N-Oxide
A
isoquinolin-5-ylamine
B
1,2,3,4-tetrahydroisoquinolin-5-amine
Conditions | Yield |
---|---|
With hydrogenchloride; palladium on activated charcoal Hydrogenation; |
5-Nitroisoquinoline N-Oxide
A
isoquinolin-5-ylamine
Conditions | Yield |
---|---|
With palladium on activated charcoal; ethanol Hydrogenation; |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: KNO3, H2SO4, aq. Na2CO3 / 25 °C 2: H2 / Pd-C / methanol View Scheme | |
Multi-step reaction with 2 steps 1.1: potassium nitrate; sulfuric acid / -15 - 20 °C 1.2: 0 °C / pH 8 2.1: ammonium chloride; iron / ethanol; water / 10 h / 80 °C View Scheme | |
Multi-step reaction with 2 steps 1: sulfuric acid; potassium nitrate / 2 h / -15 - 20 °C 2: iron; ammonium chloride / ethanol; water / 10 h / 20 - 80 °C View Scheme | |
Multi-step reaction with 2 steps 1: sulfuric acid; potassium nitrate / 2 h / -15 - 20 °C 2: ammonium chloride; iron / ethanol; water / 10 h / 20 - 80 °C View Scheme | |
Multi-step reaction with 2 steps 1: potassium nitrate; sulfuric acid / 2 h / 0 °C 2: tin(ll) chloride; hydrogenchloride / water / 1 h / Reflux View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 86 percent / conc. H2SO4, KNO3 / 6 h / 50 °C 2: 79 percent / activated carbon, FeCl3*6H2O, hydrazine / methanol / 16 h / Heating View Scheme |
1-chloro-5-nitroisoquinoline
isoquinolin-5-ylamine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: Raney nickel / Hydrogenation 2: Raney nickel; ethanolic NaOH; H2ptcl6 / Hydrogenation View Scheme |
1-chloroisoquinoline
isoquinolin-5-ylamine
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: concentrated sulfuric acid; potassium nitrate 2: Raney nickel / Hydrogenation 3: Raney nickel; ethanolic NaOH; H2ptcl6 / Hydrogenation View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: concentrated sulfuric acid; potassium nitrate 2: palladium/charcoal; aq.-ethanolic HCl / Hydrogenation View Scheme | |
Multi-step reaction with 2 steps 1: concentrated sulfuric acid; potassium nitrate 2: palladium/charcoal; aq.-ethanolic HCl / Hydrogenation View Scheme | |
Multi-step reaction with 2 steps 1: concentrated sulfuric acid; potassium nitrate 2: palladium/charcoal; ethanol / Hydrogenation View Scheme |
isoquinolin-5-ylamine
hexakis(4-formylphenoxy)cyclotriphosphazene
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; for 24h; | 100% |
Conditions | Yield |
---|---|
In acetone at 20℃; for 2h; | 100% |
Conditions | Yield |
---|---|
With pyridine at 20℃; | 99% |
In pyridine at 20℃; | 94% |
for 20h; Ambient temperature; | 80% |
2,2-dimethylsuccinic anhydride
isoquinolin-5-ylamine
1-(isoquinolin-5-yl)-3,3-dimethylpyrrolidine-2,5-dione
Conditions | Yield |
---|---|
at 150℃; neat (no solvent); | 99% |
isoquinolin-5-ylamine
Benzoyl isothiocyanate
1-benzoyl-3-isoquinolin-5-yl-thiourea
Conditions | Yield |
---|---|
In acetone at 20℃; for 1h; | 98% |
isoquinolin-5-ylamine
phenyl chloroformate
(isoquinolin-5-yl)carbamic acid phenyl ester
Conditions | Yield |
---|---|
Stage #1: isoquinolin-5-ylamine With pyridine In acetonitrile at 20℃; Stage #2: phenyl chloroformate In acetonitrile at 20℃; for 1h; | 97% |
With sodium hydrogencarbonate In dichloromethane | 92% |
at 0 - 20℃; | 72% |
isoquinolin-5-ylamine
5-azidoisoquinoline
Conditions | Yield |
---|---|
Stage #1: isoquinolin-5-ylamine With sulfuric acid In water at 0℃; for 0.0833333h; Stage #2: With sodium azide In water at 20℃; for 0.166667h; | 96.9% |
Stage #1: isoquinolin-5-ylamine With hydrogenchloride; sodium nitrite In water at 0℃; for 1h; Stage #2: With sodium azide; sodium acetate In water at 20℃; for 15h; | 95% |
With hydrogenchloride; sodium azide; sodium acetate; sodium nitrite 1.) water, 5 deg C; Yield given. Multistep reaction; | |
Stage #1: isoquinolin-5-ylamine With hydrogenchloride; sodium nitrite In water at 0 - 5℃; for 0.5h; Stage #2: With sodium azide In water at 0 - 20℃; |
isoquinolin-5-ylamine
1-isothiocyanato-3-trifluoromethyl-benzene
1-(isoquinolin-5-yl)-3-(3-(trifluoromethyl)phenyl)thiourea
Conditions | Yield |
---|---|
In tetrahydrofuran; toluene at 60℃; | 96% |
isoquinolin-5-ylamine
3,5-dichlorophenylisothiocyanate
1-(3,5-dichlorophenyl)-3-(isoquinolin-5-yl)thiourea
Conditions | Yield |
---|---|
In tetrahydrofuran; toluene at 60℃; | 96% |
isoquinolin-5-ylamine
formaldehyd
cyclopenta-1,3-diene
(6aS,9aR)-6,6a,7,9a-Tetrahydro-5H-cyclopenta[c][1,8]phenanthroline
Conditions | Yield |
---|---|
With trifluoroacetic acid In water; acetonitrile for 1h; Ambient temperature; | 95% |
With trifluoroacetic acid In acetonitrile for 0.166667h; Ambient temperature; | 95% |
Triallylborane
isoquinolin-5-ylamine
Conditions | Yield |
---|---|
Stage #1: Triallylborane; isoquinolin-5-ylamine In benzene for 0.5h; Heating; Stage #2: With isopropyl alcohol for 2h; Heating; Stage #3: With sodium hydroxide | 95% |
isoquinolin-5-ylamine
6-chloropiperonal
Conditions | Yield |
---|---|
In various solvent(s) for 24h; Heating; | 95% |
isoquinolin-5-ylamine
propionic acid anhydride
N-(5-isoquinolinyl)propionamide
Conditions | Yield |
---|---|
With pyridine at 20℃; | 95% |
With pyridine at 20℃; for 24h; Inert atmosphere; | 82% |
isoquinolin-5-ylamine
p-Tolylisocyanate
1-(isoquinolin-5-yl)-3-p-tolylurea
Conditions | Yield |
---|---|
In tetrahydrofuran; toluene at 60℃; | 95% |
Conditions | Yield |
---|---|
With pyridine at 0℃; for 2h; Inert atmosphere; | 95% |
Conditions | Yield |
---|---|
With tetrabutylammomium bromide; sodium carbonate; sulfur In water at 80℃; for 5h; | 95% |
Stage #1: carbon disulfide; isoquinolin-5-ylamine With triethylamine In tetrahydrofuran at 20℃; Stage #2: With dmap; di-tert-butyl dicarbonate In tetrahydrofuran at 0 - 20℃; | 100 %Chromat. |
isoquinolin-5-ylamine
p-ethoxycarbonylphenyl isocyanate
Conditions | Yield |
---|---|
With triethylamine In 1,4-dioxane at 90℃; | 95% |
Conditions | Yield |
---|---|
In acetonitrile at 70 - 75℃; for 11h; Inert atmosphere; | 95% |
In acetonitrile at 70 - 75℃; for 11h; Temperature; chemoselective reaction; | 95% |
Conditions | Yield |
---|---|
In methanol for 5h; Reflux; | 94% |
Conditions | Yield |
---|---|
In neat (no solvent) at 120℃; under 1500.15 Torr; for 0.166667h; Microwave irradiation; | 94% |
Conditions | Yield |
---|---|
With pyridine at 20℃; | 93% |
isoquinolin-5-ylamine
Ethyl isothiocyanate
N-ethyl-N1-(5-isoquinolinyl)thiourea
Conditions | Yield |
---|---|
In methanol for 10h; Reflux; | 92% |
In tetrahydrofuran | 34% |
isoquinolin-5-ylamine
o-fluorophenyl isothiocyanate
1-(2-fluorophenyl)-3-(isoquinolin-5-yl)thiourea
Conditions | Yield |
---|---|
In tetrahydrofuran; toluene at 60℃; | 92% |
isoquinolin-5-ylamine
p-nitrophenyl isothiocyanate
1-(isoquinolin-5-yl)-3-(4-nitrophenyl)thiourea
Conditions | Yield |
---|---|
In tetrahydrofuran; toluene at 60℃; | 92% |
isoquinolin-5-ylamine
3-oxo-pyrrolidine-1-carboxylic acid tert-butyl ester
N-(pyrrolidin-3-yl)isoquinolin-5-amine
Conditions | Yield |
---|---|
Stage #1: isoquinolin-5-ylamine; 3-oxo-pyrrolidine-1-carboxylic acid tert-butyl ester With sodium tris(acetoxy)borohydride In acetic acid at 0 - 20℃; Stage #2: With hydrogenchloride In diethyl ether for 6h; | 92% |
isoquinolin-5-ylamine
1-oxa-3,6-dithiacycloheptane
Conditions | Yield |
---|---|
Stage #1: 1-oxa-3,6-dithiacycloheptane With samarium(III) nitrate hexahydrate In chloroform at 20℃; for 0.5h; Inert atmosphere; Stage #2: isoquinolin-5-ylamine In ethanol; chloroform at 20℃; for 3h; Inert atmosphere; | 92% |
Conditions | Yield |
---|---|
With 1,1,1,3',3',3'-hexafluoro-propanol at 25℃; for 2h; regioselective reaction; | 92% |
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