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Cas:957-77-7
Min.Order:5 Kiloliter
FOB Price: $1.2 / 5.0
Type:Manufacturers
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Cas:957-77-7
Min.Order:1 Kilogram
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Cas:957-77-7
Min.Order:1 Kilogram
FOB Price: $139.0 / 210.0
Type:Trading Company
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NewCan Biotech Limited was established in 2021 and is primarily engaged in the research, development, production, and sales of sugars, nucleosides, nucleotides, phosphorylated monomers, as well as next-generation antiviral and antitumor drug intermed
A 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:957-77-7
Min.Order:4 Kilogram
Negotiable
Type:Lab/Research institutions
inquiryProduct Details Grade: pharmaceutical grade Purity:99%+ ProductionCapacity: 1000 Kilogram/Month Scope of use: For scientific research only(The product must be used legally) Our Advantage 1. Best quality with competitive price. 2. Quick shipping,
SAGECHEM is a chemical R&D, manufacturing and distribution company in China since 2009, including pharmaceutical intermediates, agrochemical, dyestuff intermediates, organosilicone, API and etc. We also offer a full range of services in custom synthe
Cas:957-77-7
Min.Order:0
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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
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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Stock products, own laboratory Package:Grams, Kilograms Application:For R&D Transportation:According to customer request Port:Shanghai
factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
Best Seller, High Quality, Competitive Price, Fast Delivery, Quick ResponseAppearance:powder, or liquid Storage:Stored in room temperature, ventilated place Package:Bottle, barrel, cargo, container, etc. Application:Pharmaceuticals, intermediates, AP
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Min.Order:10 Milligram
Negotiable
Type:Lab/Research institutions
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COA,H-NMR,HPLC availableWe have offices in Boston,MA,USAWe ship it in real nameMerck and Sigma are our customersPayment:Credit card/Net 30 daysWeb:www.alliconpharma.com Storage:Store in a cool, dry, well-ventilated area away from incompatible substan
FINETECH INDUSTRY LIMITED is a LONDON based CRO company providing drug discovery & development services to worldwide clients. FINETECH INDUSTRY LIMITED supplies the 5-HYDROXYURIDINE, CAS:957-77-7 with the most competitive price and the best quality.
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
5-bromouridine
A
5',6-anhydro-6-hydroxyuridine
B
1-(β-D-ribofuranosyl)-2-oxo-4-imidazoline-4-carboxylic acid
C
5-Hydroxy-uridin
D
6-hydroxyuridine
Conditions | Yield |
---|---|
With sodium hydroxide at 90.1℃; Rate constant; Mechanism; various reagent concentration; |
5-Hydroxy-uridin
2-(triphenylphosphoranylidene)acetamide
5-(carbamoylmethyl)uridine
Conditions | Yield |
---|---|
In 1,4-dioxane Heating; | 99% |
Acetyl bromide
5-Hydroxy-uridin
A
1-(2-bromo-2-deoxy-3,5-di-O-acetylribosyl)-5-acetoxyuracil
Conditions | Yield |
---|---|
In acetonitrile at 60℃; | A 95% B 5% |
5-Hydroxy-uridin
2,2-dimethoxy-propane
2',3'-O-isopropylidene-5-hydroxyuridine
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid for 48h; Ambient temperature; | 84% |
Acetyl bromide
5-Hydroxy-uridin
A
1-(2-bromo-2-deoxy-3,5-di-O-acetylribosyl)-5-acetoxyuracil
C
O3',O5'-diacetyl-5,2'-dibromo-2'-deoxy-uridine
Conditions | Yield |
---|---|
With hydrogen bromide; acetic acid In acetonitrile at 60℃; | A 76% B 5% C 16% |
5-Hydroxy-uridin
methyl (triphenylphosphoranylidene)acetate
5-<(methylcarboxy)methyl>uridine
Conditions | Yield |
---|---|
In 1,4-dioxane Heating; | 67% |
5-Hydroxy-uridin
chlorodimethyl(1,1,2-trimethylpropyl)silane
5'-O-(silyl)-5-(siloxy)uridine
Conditions | Yield |
---|---|
With pyridine for 50h; Ambient temperature; | 65% |
5-Hydroxy-uridin
Conditions | Yield |
---|---|
With sodium azide In tetrahydrofuran at 80℃; for 5h; | 62% |
Conditions | Yield |
---|---|
Stage #1: 5-Hydroxy-uridin With N-Bromosuccinimide In ethanol at 20℃; for 0.5h; Stage #2: 2-amino-benzenethiol In ethanol for 1h; Heating; | 59% |
Conditions | Yield |
---|---|
With sodium hydroxide In methanol; water at 25℃; for 12h; | A 12% B 57% |
Conditions | Yield |
---|---|
With sodium hydroxide In water for 16h; Ambient temperature; | 54% |
5-Hydroxy-uridin
2,2-dimethoxy-propane
acetone
A
2',3'-O-isopropylidene-5-hydroxyuridine
B
2',3'-O-isopropylidene-5'-O-(2-methoxy-2-propyl)-5-hydroxyuridine
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid for 22h; Ambient temperature; | A 37% B 30% |
5-Hydroxy-uridin
triethylamine carbonate
Conditions | Yield |
---|---|
Stage #1: 5-Hydroxy-uridin With trimethyl phosphite; N,N,N',N'-tetramethyl-1,8-diaminonaphthalene at 0℃; for 0.166667h; Stage #2: With trichlorophosphate for 2h; Inert atmosphere; Stage #3: triethylamine carbonate Further stages; | 4.13% |
5-Hydroxy-uridin
triethylamine carbonate
Conditions | Yield |
---|---|
Stage #1: 5-Hydroxy-uridin With N,N,N',N'-tetramethyl-1,8-diaminonaphthalene at 0℃; for 0.166667h; Stage #2: With trichlorophosphate for 2h; Inert atmosphere; Stage #3: triethylamine carbonate Further stages; | 4.13% |
5-Hydroxy-uridin
4-amino-2,2,6,6-tetramethyl-1-piperidine-1-oxyl
Conditions | Yield |
---|---|
With sulfuric acid In water for 7.5h; | 30 mg |
Conditions | Yield |
---|---|
With sulfuric acid In water for 6h; | 24 mg |
Conditions | Yield |
---|---|
With sulfuric acid In water for 6h; | 44 mg |
5-Hydroxy-uridin
1-(β-D-ribofuranosyl)-2-oxo-4-imidazoline-4-carboxylic acid
Conditions | Yield |
---|---|
With sodium hydroxide at 90.1℃; Rate constant; decomposition, various reagent concentration; |
(tert-Butoxycarbonylmethylene)triphenylphosphorane
5-Hydroxy-uridin
[1-((2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-2,4-dioxo-1,2,3,4-tetrahydro-pyrimidin-5-yl]-acetic acid tert-butyl ester
Conditions | Yield |
---|---|
In 1,4-dioxane for 9h; Heating; | 2.59 g |
5-Hydroxy-uridin
(2R,3R,4R,5R)-2-(acetoxymethyl)-5-(5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)tetrahydrofuran-3,4-diyl diacetate
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 2.59 g / dioxane / 9 h / Heating 2: 2.55 g / pyridine / 16 h / Ambient temperature 3: 68 percent / TFA / CH2Cl2 / 1 h / Ambient temperature View Scheme |
5-Hydroxy-uridin
2',3',5'-tri-O-acetyl-5-t-butoxycarbonylmethyluridine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 2.59 g / dioxane / 9 h / Heating 2: 2.55 g / pyridine / 16 h / Ambient temperature View Scheme |
5-Hydroxy-uridin
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 65 percent / pyridine / 50 h / Ambient temperature 2: 63 percent / dimethylformamide / Ambient temperature View Scheme |
5-Hydroxy-uridin
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 65 percent / pyridine / 50 h / Ambient temperature 2: 12 percent / dimethylformamide / Ambient temperature 3: 73 percent / P(OCH3)3 / 3 h / Heating View Scheme | |
Multi-step reaction with 3 steps 1: 65 percent / pyridine / 50 h / Ambient temperature 2: 74 percent / 1,2-dichloro-ethane / 4 h / Ambient temperature 3: 73 percent / P(OCH3)3 / 3 h / Heating View Scheme |
5-Hydroxy-uridin
5'-O-(silyl)-2',3'-O-thiocarbonyl-5-(siloxy)uridine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 65 percent / pyridine / 50 h / Ambient temperature 2: 12 percent / dimethylformamide / Ambient temperature View Scheme | |
Multi-step reaction with 2 steps 1: 65 percent / pyridine / 50 h / Ambient temperature 2: 74 percent / 1,2-dichloro-ethane / 4 h / Ambient temperature View Scheme |
5-Hydroxy-uridin
2',3'-O-isopropylidene-5-(ethoxycarbonylmethoxy)uridine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 84 percent / p-TosOH / 48 h / Ambient temperature 2: 48 percent / 1 M NaOH / aq. ethanol / 3 h / Ambient temperature View Scheme |
5-Hydroxy-uridin
2',3'-O-isopropylidene-2,5'-anhydro-5-(ethoxycarbonylmethoxy)uridine
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 84 percent / p-TosOH / 48 h / Ambient temperature 2: 48 percent / 1 M NaOH / aq. ethanol / 3 h / Ambient temperature 3: 90 percent / (C6H5)3P, (C2H5)3N, ethyl azadicarboxylate / dioxane / 3 h View Scheme |
5-Hydroxy-uridin
2',3'-O-isopropylidene-5-ethoxycarbonylmethoxy-2-thiouridine
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: 84 percent / p-TosOH / 48 h / Ambient temperature 2: 48 percent / 1 M NaOH / aq. ethanol / 3 h / Ambient temperature 3: 90 percent / (C6H5)3P, (C2H5)3N, ethyl azadicarboxylate / dioxane / 3 h 4: 32 percent / H2S / pyridine / 120 h / Ambient temperature View Scheme |
5-Hydroxy-uridin
uridine 5-oxyacetic acid methyl ester
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 84 percent / p-TosOH / 48 h / Ambient temperature 2: 48 percent / 1 M NaOH / aq. ethanol / 3 h / Ambient temperature 3: 83 percent / 1 M HCl / 48 h / Ambient temperature View Scheme |
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