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Cas:88192-20-5
Min.Order:0
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Type:Lab/Research institutions
inquiryA substitute for perfluorooctanoic acid, mainly used as a surfactant, dispersant, additive, etc Appearance:White solid or Colorless liquid Purity:99.3 % We will ship the goods in a timely manner as required We can provide relevant documents acc
Cas:88192-20-5
Min.Order:4 Kilogram
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Type:Lab/Research institutions
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Cas:88192-20-5
Min.Order:1 Kilogram
FOB Price: $2.0
Type:Lab/Research institutions
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Cas:88192-20-5
Min.Order:1 Metric Ton
FOB Price: $1.0
Type:Trading Company
inquiryHunan chemfish Pharmaceutical co.,Ltd.located in Lugu High-tech industral park ,Hunan province . with its own R&D center and more than 10000㎡manufacture plant . Chemfish owns 40 reactors from 1000L to 8000L. With complete auxiliary equipment as
Our own factory produces direct sales with absolute price advantage Application:Pharmaceutical industry Transportation:By sea Port:Shanghai/tianjin
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Cas:88192-20-5
Min.Order:0
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Type:Trading Company
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factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
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Cas:88192-20-5
Min.Order:500 Gram
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Type:Lab/Research institutions
inquiryFINETECH INDUSTRY LIMITED is a LONDON based CRO company providing drug discovery & development services to worldwide clients. FINETECH INDUSTRY LIMITED supplies the 4-Azidobutan-1-amine, CAS:88192-20-5 with the most competitive price and the best qua
1.Company Profile Established in 2018, Xi'an Confluore Biological Technology Co., Ltd. is a high-tech enterprise that develops and sells cutting-edge chemical reagents and biological reagents for scientific research. The company provides high-qu
Cas:88192-20-5
Min.Order:0 Metric Ton
Negotiable
Type:Lab/Research institutions
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Debyesci is here who supplied several kinds of chemical products to global pharmaceutical, drug discovery, agrochemical and biotechnology industries for four yearsOur key scientific leadership team has gained experience in top research and developmen
1,4-diazidobutane
4-azidobutan-1-amine
Conditions | Yield |
---|---|
With hydrogenchloride; triphenylphosphine In diethyl ether; water; ethyl acetate at 20℃; for 24h; | 88% |
With hydrogenchloride; water; triphenylphosphine In diethyl ether; ethyl acetate at 0 - 20℃; for 25h; | 88% |
With hydrogenchloride; triphenylphosphine In diethyl ether; water; ethyl acetate at 0 - 20℃; for 25h; Inert atmosphere; | 88% |
1-azido-4-isocyanatobutane
4-azidobutan-1-amine
Conditions | Yield |
---|---|
With sodium hydroxide In tetrahydrofuran for 4h; Heating; | 83% |
N-(4-azidobutyl)phthalimide
4-azidobutan-1-amine
Conditions | Yield |
---|---|
With hydrazine hydrate In ethanol for 24h; | 62% |
With hydrazine hydrate In tetrahydrofuran at 60℃; for 4h; | |
With hydrazine In methanol Inert atmosphere; |
1,4-diaminobutane
4-azidobutan-1-amine
Conditions | Yield |
---|---|
With triflic azide; potassium carbonate; copper(II) sulfate In methanol; water | 61% |
4-azidobutan-1-amine
Conditions | Yield |
---|---|
With sodium azide In water at 80℃; for 15h; | 50% |
Conditions | Yield |
---|---|
With triflic azide; potassium carbonate; copper(II) sulfate In water for 18h; Inert atmosphere; | A 30% B 40% |
N-t-butoxycarbonyl-4-azidobutylamine
4-azidobutan-1-amine
Conditions | Yield |
---|---|
With hydrogenchloride In ethyl acetate at 20℃; for 72h; | |
With trifluoroacetic acid In dichloromethane at 20℃; for 16h; |
1,4-diazidobutane
triphenylphosphine
A
4-azidobutan-1-amine
B
Triphenylphosphine oxide
Conditions | Yield |
---|---|
With hydrogenchloride; water In diethyl ether; hexane at 0℃; modified Staudinger reaction; |
1,4-dibromo-butane
4-azidobutan-1-amine
Conditions | Yield |
---|---|
With sodium azide In water; N,N-dimethyl-formamide at 80 - 85℃; for 8h; | 343.7 g |
Stage #1: 1,4-dibromo-butane With sodium azide In water; N,N-dimethyl-formamide at 80 - 90℃; for 12h; Stage #2: With hydrogenchloride; triphenylphosphine In water at 25 - 35℃; for 12h; |
1-bromo-4-aminobutane
4-azidobutan-1-amine
Conditions | Yield |
---|---|
With sodium azide In water at 80℃; | 620 mg |
di-tert-butyl dicarbonate
4-azidobutan-1-amine
N-t-butoxycarbonyl-4-azidobutylamine
Conditions | Yield |
---|---|
With sodium hydroxide In tetrahydrofuran; water | 100% |
benzyl chloroformate
4-azidobutan-1-amine
4-azido-N-benzyloxycarbonyl-1-butylamine
Conditions | Yield |
---|---|
With sodium hydroxide In tetrahydrofuran; water at 0 - 20℃; for 12h; | 100% |
2-Nitrobenzenesulfonyl chloride
4-azidobutan-1-amine
Conditions | Yield |
---|---|
With sodium hydroxide In tetrahydrofuran; water | 100% |
p-toluenesulfonyl chloride
4-azidobutan-1-amine
Conditions | Yield |
---|---|
With sodium hydroxide In tetrahydrofuran; water | 100% |
2-hydroxy-2-methylpropanenitrile
4-azidobutan-1-amine
2-(4-azidobutylamino)-2-methylpropionitrile
Conditions | Yield |
---|---|
With sodium sulfate at 21℃; for 12h; Inert atmosphere; | 99% |
3-acetylenephenylamine
4-azidobutan-1-amine
Conditions | Yield |
---|---|
With copper(II) sulfate; sodium L-ascorbate | 95% |
indomethacin pentafluorophenyl ester
4-azidobutan-1-amine
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 2h; Inert atmosphere; | 94% |
Conditions | Yield |
---|---|
In ethanol for 0.5h; | 94% |
1,2-bis(bromomethyl)-4,5-dimethoxybenzene
4-azidobutan-1-amine
2-(4-azidobutyl)-5,6-dimethoxyisoindoline
Conditions | Yield |
---|---|
With potassium carbonate; sodium iodide In N,N-dimethyl-formamide at 60℃; for 3h; | 93% |
Conditions | Yield |
---|---|
With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In dimethyl sulfoxide; N,N-dimethyl-formamide at 0 - 23℃; | 93% |
Conditions | Yield |
---|---|
In tert-butyl methyl ether at 20 - 25℃; for 16h; | 92% |
N-(prop-2-ynyl)-2-(4-(trifluoromethyl)phenyl)diazenecarboxamide
4-azidobutan-1-amine
N-((1-(4-aminobutyl)-1H-1,2,3-triazol-4-yl)methyl)-2-(4-(trifluoromethyl)phenyl)diazenecarboxamide
Conditions | Yield |
---|---|
With copper(ll) sulfate pentahydrate In methanol; water at 20℃; for 0.0833333h; Inert atmosphere; regioselective reaction; | 91% |
2',3'-O-isopropylideneinosine
4-azidobutan-1-amine
N6-(4"-azidobutyl)-2',3'-(O-isopropylidene)adenosine
Conditions | Yield |
---|---|
With benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In acetonitrile Inert atmosphere; | 91% |
2',3'-O-isopropylidene inosine
4-azidobutan-1-amine
N6-(4"-azidobutyl)-2',3'-(O-isopropylidene)adenosine
Conditions | Yield |
---|---|
Stage #1: 2',3'-O-isopropylidene inosine With benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In acetonitrile at 20℃; Inert atmosphere; Stage #2: 4-azidobutan-1-amine In acetonitrile at 20℃; Inert atmosphere; | 91% |
Conditions | Yield |
---|---|
In tert-butyl methyl ether at 20 - 25℃; for 16h; | 91% |
4-azidobutan-1-amine
putrescine dihydrochloride
Conditions | Yield |
---|---|
With hydrogenchloride; hydrogen; palladium on activated charcoal In methanol under 3102.9 Torr; for 18h; Ambient temperature; | 90% |
4-azidobutan-1-amine
4-(1-pyrene)butyric acid N-hydroxysuccinimide ester
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; for 3h; | 88% |
ethacrynic acid
4-azidobutan-1-amine
1-{4-[(4-azidobutylaminooxy)methyl]-2,3-dichlorophenyl}-2-methylenebutan-1-one
Conditions | Yield |
---|---|
With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide for 1h; Inert atmosphere; | 86% |
fluoresceinyl 5-isothiocyanate
4-azidobutan-1-amine
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 20℃; for 12h; | 86% |
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran at 20℃; for 18h; | 82% |
3-(p-phenyl)benzoylpropionic acid
4-azidobutan-1-amine
N-(4-azidobutyl)-4-(biphenyl-4-yl)-4-oxobutanamide
Conditions | Yield |
---|---|
With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide for 1h; Inert atmosphere; | 77% |
With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 60℃; for 1h; | 77% |
4-azidobutan-1-amine
5'(S)-[O4-(2,4,6-triisopropylbenzenesulfonyl)uracil-1-yl]-1',3'-oxathiolane-2'(R)-carboxylic acid (1R,2S,5R)-menthyl ester
5'(S)-{N4-[1-(4-azidobutyl)]cytosin-1-yl}-1',3'-oxathiolane-2'(R)-carboxylic acid (1R,2S,5R)-menthyl ester
Conditions | Yield |
---|---|
In dichloromethane at 0℃; for 0.75h; | 76% |
O,O'-dibenzoyl-D-tartaric acid
4-azidobutan-1-amine
Conditions | Yield |
---|---|
In tert-butyl methyl ether at 20 - 25℃; for 16h; | 75% |
Conditions | Yield |
---|---|
In water; acetonitrile at 55 - 65℃; | 75% |
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate In tetrahydrofuran at 0 - 20℃; | 75% |
(1'S,2'R,3'S,4'R,5'S)-4'-[6-(3-chlorobenzylamino)-2-(1,7-octadiynyl)-9H-purin-9-yl]-2',3'-dihydroxybicyclo[3.1.0]hexane-1'-carboxylic acid N-methylamide
4-azidobutan-1-amine
(1S,2R,3S,4R,5S)-4-(6-(3-chlorobenzylamino)-2-(6-(1-(4-aminobutyl)-1H-1,2,3-triazol-4-yl)hex-1-ynyl)-9H-purin-9-yl)-2,3-dihydroxybicyclo[3.1.0]hexane-1-carboxylic acid N-methylamide
Conditions | Yield |
---|---|
With copper(II) sulphate hydrate; sodium L-ascorbate; tris[(1-benzyl-1H-1,2,3-triazol-4yl)methyl]amine In water; tert-butyl alcohol at 20℃; regioselective reaction; | 73% |
4-azidobutan-1-amine
4-azido-1-butanol
Conditions | Yield |
---|---|
With sodium azide; trifluoromethylsulfonic anhydride In dichloromethane; water | 70% |
thiophene-2-carbaldehyde
4-azidobutan-1-amine
Conditions | Yield |
---|---|
Stage #1: thiophene-2-carbaldehyde; 4-azidobutan-1-amine With triethylamine In methanol for 12h; Inert atmosphere; Reflux; Stage #2: With sodium tetrahydroborate In methanol at 0℃; for 1h; Inert atmosphere; | 70% |
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