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Cas:59587-07-4
Min.Order:1 Kilogram
FOB Price: $3.0
Type:Lab/Research institutions
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Cas:59587-07-4
Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
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Cas:59587-07-4
Min.Order:1 Metric Ton
FOB Price: $7.0 / 8.0
Type:Trading Company
inquiryAnsciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali
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2-Azidoadenosine cas 59587-07-4Appearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express
factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
Good Quality Package:1kg/bag Application:Medical or chemical Transportation:Air/Train/Sea Port:Shenzhen
factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
Price, service, company and transport advantage: 1. Best service, place of origin China, high quality, and reasonable price. 2. It's customers' right to choose the package (EMS, DHL, FEDEX, UPS). 3. It's customers' right
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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 2-Azido Adenosine, CAS:59587-07-4 with the most competitive price and the best qualit
Adenosine, 2-azido-Appearance:Off white to slight yellow solid Storage:Store in dry and cool condition Package:25kg or according to cutomer's demand Application:Chemical research/Pharmaceutical intermediates Transportation:By Sea,by Air,By courier li
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Adenosine, 2-azido-Appearance:Off white to slight yellow solid Storage:Stored in shaded, cool and dry places Package:1L 5L 10L 25L bottle Application:pharma intermediate Transportation:Handle with cares to avoid damaging the packages. Protect them fr
Acetic acid (2R,3R,4R,5R)-4-acetoxy-5-acetoxymethyl-2-(2-azido-6-chloro-purin-9-yl)-tetrahydro-furan-3-yl ester
2-Azidoadenosine
Conditions | Yield |
---|---|
With ammonia In ethanol at 30℃; for 48h; | 89% |
2-Chloroadenosine
2-Azidoadenosine
Conditions | Yield |
---|---|
Stage #1: 2-Chloroadenosine With hydrazine hydrate at 20℃; for 16h; Stage #2: With acetic acid; sodium nitrite In water for 1h; cooling; | 61% |
Multi-step reaction with 2 steps 1: H2NNH2*H2O / 20 °C 2: NaNO2; acetic acid / H2O / 0 °C View Scheme |
2-Azidoadenosine
Conditions | Yield |
---|---|
With acetic acid; sodium nitrite |
2-hydrazinoadenosine
2-Azidoadenosine
Conditions | Yield |
---|---|
With acetic acid; sodium nitrite In water at 0℃; |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1.1: SnCl4 / acetonitrile / 20 °C 2.1: NH3 / methanol / 20 °C 3.1: hydrazine monohydrate / 16 h / 20 °C 3.2: 61 percent / sodium nitrite; acetic acid / H2O / 1 h / cooling View Scheme |
(2R,3R,4R,5R)-2-((benzoyloxy)methyl)-5-(2,6-dichloro-9H-purin-9-yl)tetrahydrofuran-3,4-diyl dibenzoate
2-Azidoadenosine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: NH3 / methanol / 20 °C 2.1: hydrazine monohydrate / 16 h / 20 °C 2.2: 61 percent / sodium nitrite; acetic acid / H2O / 1 h / cooling View Scheme |
2,6 dichloropurine
2-Azidoadenosine
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1.1: SnCl4 / acetonitrile / 20 °C 2.1: NH3 / methanol / 20 °C 3.1: hydrazine monohydrate / 16 h / 20 °C 3.2: 61 percent / sodium nitrite; acetic acid / H2O / 1 h / cooling View Scheme |
2-amino-6-chloro-9-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)purine
2-Azidoadenosine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 75 percent / isoamyl nitrite, trimethylsilyl azide / acetonitrile / 1) -20 deg C, 12 h; 2) 0 deg C, 2 d 2: 89 percent / NH3 / ethanol / 48 h / 30 °C View Scheme |
G
2-Azidoadenosine
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: pyridine / dimethylformamide 2: POCl, Et4NCl, N,N-dimethylaniline / acetonitrile 3: 75 percent / isoamyl nitrite, trimethylsilyl azide / acetonitrile / 1) -20 deg C, 12 h; 2) 0 deg C, 2 d 4: 89 percent / NH3 / ethanol / 48 h / 30 °C View Scheme |
2',3',5'-tri-O-acetyl-guanosine
2-Azidoadenosine
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: POCl, Et4NCl, N,N-dimethylaniline / acetonitrile 2: 75 percent / isoamyl nitrite, trimethylsilyl azide / acetonitrile / 1) -20 deg C, 12 h; 2) 0 deg C, 2 d 3: 89 percent / NH3 / ethanol / 48 h / 30 °C View Scheme |
2-Azidoadenosine
Conditions | Yield |
---|---|
With methanol; ammonia at 50℃; for 15h; Inert atmosphere; |
2-Azidoadenosine
Conditions | Yield |
---|---|
With trimethyl phosphite; tri(n-butyl)ammonium pyrophosphate; trichlorophosphate | 58% |
2-Azidoadenosine
Conditions | Yield |
---|---|
With trimethyl phosphite; (Bu3NH)4*(PO3)2NH; trichlorophosphate | 58% |
2-Azidoadenosine
Conditions | Yield |
---|---|
In dimethylsulfoxide-d6 at 24.85℃; Equilibrium constant; Thermodynamic data; Further Variations:; Solvents; Temperatures; |
2-Azidoadenosine
2,2-dimethoxy-propane
2-azido-2',3'-O-isopropylideneadenosine
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In acetone at 20℃; for 16h; Inert atmosphere; | 1.57 g |
(3-(5H,6H-11,12-didehydrodibenzo[b,f]azocin-5-yl)-3-oxopropyl)amine
2-Azidoadenosine
Conditions | Yield |
---|---|
In methanol at 20℃; for 16h; |
Conditions | Yield |
---|---|
In water; acetonitrile at 20℃; for 2h; Overall yield = 100 %; Overall yield = 9.3 mg; |
triethylamine carbonate
2-Azidoadenosine
Conditions | Yield |
---|---|
Stage #1: 2-Azidoadenosine With trimethyl phosphite; N,N,N',N'-tetramethyl-1,8-diaminonaphthalene; trichlorophosphate In acetonitrile at 0℃; Stage #2: triethylamine carbonate In acetonitrile at 0℃; for 0.5h; | A 60 %Spectr. B 40 %Chromat. |
triethylamine carbonate
2-Azidoadenosine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: trichlorophosphate; trimethyl phosphite; N,N,N',N'-tetramethyl-1,8-diaminonaphthalene / acetonitrile / 0 °C 1.2: 0.5 h / 0 °C 2.1: triethylamine; 1,1'-carbonyldiimidazole / N,N-dimethyl-formamide / 4 h / 20 °C 2.2: 96 h / 20 °C View Scheme |
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