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SALACINOLEXTRACT CAS:200399-47-9 Qingdao Belugas Import and Export Co., Ltd. is a scientific and technological company integrating research and development, production and trade of chemical intermediates, specializing in high quality organic interme
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Henan 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
Zibo Hangyu Biotechnology Development Co., Ltd is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemi
Superior quality, moderate price & quick delivery. Appearance:white powder Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:1kg/bag, 1kg/drum or 25kg/drum or as per your request. Application:Salacinol is a α-gl
About Product Technical Details CAS: 200399-47-9 MF: C9H18O9S2 MW: 334.36382 EINECS: Product Categories: Mol File: 200399-47-9.mol
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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,
Our 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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GOLDEN 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
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SalacinolAppearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:pharmaceutical intermediate Transportation:by air, by sea, by express
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inquiryCAS 200399-47-9 (1S,2S)-3-[(2R,3S,4S)-3,4-dihydroxy-2-(hydroxymethyl)tetrahydrothiophenium-1-yl]-2-hydroxy-1-(hydroxymethyl)propyl sulfate (non-preferred name) (2S,3S)-4-[(2R,3S,4S)-3,4-dihydroxy-2-(hydroxymethyl)tetrahydrothiophenium-1-yl]-1,3
Chengdu Push Bio-technology Co., Ltd. provides more than 4,000 natural monomeric substances, including approximately 6,000 products at different grades, specifications and purities. We have specialized in the R&D of medicinally active ingredients sta
United Scientific Company Located in Shanghai of China , is a competitive player in the global specialty and fine chemical market. Fenghua has both the expertise and flexibility to produce a wide range of chemicals. Focusing on developing the innovat
(2S,3S)-4-((1S,2R,3S,4S)-3,4-dihydroxy-2-(hydroxymethyl)tetrahydro-1H-thiophene-1-ium-1-yl)-1,3-dihydroxybutan-2-yl sulfate
Conditions | Yield |
---|---|
With trifluoroacetic acid at 20℃; for 0.5h; | 86% |
2,3,5-tri-O-benzyl-1,4-dideoxy-1,4-{(S)-[(2S,3S)-2,4-O-isopropylidene-3-(sulfooxy)butyl]episulfonioylidene}-D-arabinitol
(2S,3S)-4-((1S,2R,3S,4S)-3,4-dihydroxy-2-(hydroxymethyl)tetrahydro-1H-thiophene-1-ium-1-yl)-1,3-dihydroxybutan-2-yl sulfate
Conditions | Yield |
---|---|
With hydrogen; acetic acid; palladium on activated charcoal at 50℃; for 5h; | 82% |
1,4-dideoxy-1,4-{(S)-[(2S,3S)-2,4-O-isopropylidene-3-(sulfooxy)butyl]episulfonioylidene}-D-arabinitol
(2S,3S)-4-((1S,2R,3S,4S)-3,4-dihydroxy-2-(hydroxymethyl)tetrahydro-1H-thiophene-1-ium-1-yl)-1,3-dihydroxybutan-2-yl sulfate
Conditions | Yield |
---|---|
With hydrogenchloride at 40℃; for 4h; | 74% |
(2S,3S)-4-((1S,2R,3S,4S)-3,4-dihydroxy-2-(hydroxymethyl)tetrahydro-1H-thiophene-1-ium-1-yl)-1,3-dihydroxybutan-2-yl sulfate
Conditions | Yield |
---|---|
With hydrogen; palladium dihydroxide In water; acetic acid | 65% |
(2S,3S)-4-((1S,2R,3S,4S)-3,4-dihydroxy-2-(hydroxymethyl)tetrahydro-1H-thiophene-1-ium-1-yl)-1,3-dihydroxybutan-2-yl sulfate
Conditions | Yield |
---|---|
With hydrogen; palladium dihydroxide In water; acetic acid | 65% |
3-O-benzyl-1-deoxy-4-thio-D-arabino-furanose
(2S,3S)-4-((1S,2R,3S,4S)-3,4-dihydroxy-2-(hydroxymethyl)tetrahydro-1H-thiophene-1-ium-1-yl)-1,3-dihydroxybutan-2-yl sulfate
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 90 percent / sodium hydride / dimethylformamide / 0.5 h / 0 °C 2: 99 percent / potassium carbonate / various solvent(s) / 6 h / Heating 3: 82 percent / aq. acetic acid; hydrogen / Pd/C / 5 h / 50 °C View Scheme |
1,4-anhydro-2,3,5-tri-O-benzyl-4-thio-D-arabinitol
(2S,3S)-4-((1S,2R,3S,4S)-3,4-dihydroxy-2-(hydroxymethyl)tetrahydro-1H-thiophene-1-ium-1-yl)-1,3-dihydroxybutan-2-yl sulfate
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 99 percent / potassium carbonate / various solvent(s) / 6 h / Heating 2: 82 percent / aq. acetic acid; hydrogen / Pd/C / 5 h / 50 °C View Scheme | |
Multi-step reaction with 2 steps 1: 94 percent / K2CO3 / various solvent(s) / 14 h / Heating 2: 65 percent / H2 / Pd(OH)2 / acetic acid; H2O View Scheme | |
Multi-step reaction with 2 steps 1: 45 percent / K2CO3 / various solvent(s) / 14 h / Heating 2: 65 percent / H2 / Pd(OH)2 / acetic acid; H2O View Scheme |
(2R,3S,4S)-2-(hydroxymethyl)tetrahydrothiophene-3,4-diol
(2S,3S)-4-((1S,2R,3S,4S)-3,4-dihydroxy-2-(hydroxymethyl)tetrahydro-1H-thiophene-1-ium-1-yl)-1,3-dihydroxybutan-2-yl sulfate
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 87 percent / NaH / tetrahydrofuran / 13 h / 20 - 55 °C 2: 100 percent / K2CO3 / various solvent(s) / Heating 3: 86 percent / aq. trifluoroacetic acid / 0.5 h / 20 °C View Scheme | |
Multi-step reaction with 4 steps 1.1: sodium hydride / N,N-dimethyl-formamide / 0.5 h / 0 - 5 °C 1.2: 6 h / 0 - 25 °C 2.1: 2,6-dimethylpyridine / acetone / 13 h / 70 °C 3.1: diethylamine / methanol / 3 h / 25 °C 4.1: trifluoroacetic acid / water / 2 h / 25 °C View Scheme | |
Multi-step reaction with 4 steps 1.1: sodium hydride / N,N-dimethyl-formamide / 1 h / 0 - 5 °C 1.2: 3 h / 0 - 25 °C 2.1: 2,6-dimethylpyridine / acetone / 24 h / 70 °C 3.1: diethylamine / methanol / 1 h / 25 °C 4.1: hydrogen; acetic acid; 20% palladium hydroxide-activated charcoal / 2 h / 50 °C View Scheme |
(2R,3S,4S)-3,4-bis((4-methoxybenzyl)oxy)-2-(((4-methoxybenzyl)oxy)methyl)tetrahydrothiophene
(2S,3S)-4-((1S,2R,3S,4S)-3,4-dihydroxy-2-(hydroxymethyl)tetrahydro-1H-thiophene-1-ium-1-yl)-1,3-dihydroxybutan-2-yl sulfate
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 100 percent / K2CO3 / various solvent(s) / Heating 2: 86 percent / aq. trifluoroacetic acid / 0.5 h / 20 °C View Scheme | |
Multi-step reaction with 3 steps 1: 2,6-dimethylpyridine / acetone / 13 h / 70 °C 2: diethylamine / methanol / 3 h / 25 °C 3: trifluoroacetic acid / water / 2 h / 25 °C View Scheme | |
Multi-step reaction with 3 steps 1: 2,6-dimethylpyridine / acetone / 13 h / 70 °C 2: diethylamine; methanol / 3 h / 25 °C 3: water; trifluoroacetic acid / 2 h / 25 °C View Scheme | |
Multi-step reaction with 3 steps 1: 2,6-dimethylpyridine / acetone / 13 h / 70 °C 2: diethylamine / methanol / 3 h / 25 °C 3: trifluoroacetic acid / water / 2 h / 25 °C View Scheme |
(2S,3S)-4-((1S,2R,3S,4S)-3,4-dihydroxy-2-(hydroxymethyl)tetrahydro-1H-thiophene-1-ium-1-yl)-1,3-dihydroxybutan-2-yl sulfate
Conditions | Yield |
---|---|
With diethylamine In water; ethyl acetate at 25℃; for 0.833333h; Reagent/catalyst; Solvent; | 1.05 g |
With water; diethylamine In ethyl acetate at 25℃; for 0.833333h; Reagent/catalyst; Temperature; Solvent; | 1.05 g |
With diethylamine In water; ethyl acetate at 25℃; for 0.833333h; Reagent/catalyst; Solvent; Temperature; | 1.05 g |
(2S,3S)-4-((1S,2R,3S,4S)-3,4-dihydroxy-2-(hydroxymethyl)tetrahydro-1H-thiophene-1-ium-1-yl)-1,3-dihydroxybutan-2-yl sulfate
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: diethylamine; methanol / 1 h / 25 °C 2: 20% palladium hydroxide-activated charcoal; hydrogen / acetic acid / 2 h / 50 °C View Scheme |
(2S,3S)-4-((1S,2R,3S,4S)-3,4-dihydroxy-2-(hydroxymethyl)tetrahydro-1H-thiophene-1-ium-1-yl)-1,3-dihydroxybutan-2-yl sulfate
Conditions | Yield |
---|---|
With 20% palladium hydroxide-activated charcoal; hydrogen; acetic acid at 50℃; for 2h; | |
With 20% palladium hydroxide-activated charcoal; hydrogen In acetic acid at 50℃; for 2h; | |
With 20% palladium hydroxide-activated charcoal; hydrogen; acetic acid at 50℃; for 2h; |
(2S,3S)-4-((1S,2R,3S,4S)-3,4-dihydroxy-2-(hydroxymethyl)tetrahydro-1H-thiophene-1-ium-1-yl)-1,3-dihydroxybutan-2-yl sulfate
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: diethylamine / methanol / 3 h / 25 °C 2: trifluoroacetic acid / water / 2 h / 25 °C View Scheme | |
Multi-step reaction with 2 steps 1: diethylamine; methanol / 3 h / 25 °C 2: water; trifluoroacetic acid / 2 h / 25 °C View Scheme | |
Multi-step reaction with 2 steps 1: diethylamine / methanol / 3 h / 25 °C 2: trifluoroacetic acid / water / 2 h / 25 °C View Scheme |
(2S,3S)-4-((1S,2R,3S,4S)-3,4-dihydroxy-2-(hydroxymethyl)tetrahydro-1H-thiophene-1-ium-1-yl)-1,3-dihydroxybutan-2-yl sulfate
Conditions | Yield |
---|---|
With trifluoroacetic acid In water at 25℃; for 2h; | |
With water; trifluoroacetic acid at 25℃; for 2h; | |
With trifluoroacetic acid In water at 25℃; for 2h; |
(2S,3S)-4-((1S,2R,3S,4S)-3,4-dihydroxy-2-(hydroxymethyl)tetrahydro-1H-thiophene-1-ium-1-yl)-1,3-dihydroxybutan-2-yl sulfate
Conditions | Yield |
---|---|
With diethylamine In water; ethyl acetate at 25℃; for 9h; | 1.32 g |
With water; diethylamine In ethyl acetate at 25℃; for 9h; | |
With diethylamine In water; ethyl acetate at 25℃; for 9h; Reagent/catalyst; Solvent; Temperature; |
(2S,3S)-4-((1S,2R,3S,4S)-3,4-dihydroxy-2-(hydroxymethyl)tetrahydro-1H-thiophene-1-ium-1-yl)-1,3-dihydroxybutan-2-yl sulfate
Conditions | Yield |
---|---|
Multi-step reaction with 6 steps 1.1: hydrogenchloride / tetrahydrofuran; water / 1 h / 50 °C 1.2: 1.67 h / 5 - 25 °C 2.1: sodium methylate / tetrahydrofuran; methanol / 4 h / 20 °C 3.1: sodium hydride / N,N-dimethyl-formamide / 0.5 h / 0 - 5 °C 3.2: 6 h / 0 - 25 °C 4.1: 2,6-dimethylpyridine / acetone / 13 h / 70 °C 5.1: diethylamine / methanol / 3 h / 25 °C 6.1: trifluoroacetic acid / water / 2 h / 25 °C View Scheme | |
Multi-step reaction with 6 steps 1.1: hydrogenchloride / tetrahydrofuran; water / 1 h / 50 °C 1.2: 1.67 h / 5 - 25 °C 2.1: sodium methylate / tetrahydrofuran; methanol / 4 h / 20 °C 3.1: sodium hydride / N,N-dimethyl-formamide / 1 h / 0 - 5 °C 3.2: 3 h / 0 - 25 °C 4.1: 2,6-dimethylpyridine / acetone / 24 h / 70 °C 5.1: diethylamine / methanol / 1 h / 25 °C 6.1: hydrogen; acetic acid; 20% palladium hydroxide-activated charcoal / 2 h / 50 °C View Scheme | |
Multi-step reaction with 6 steps 1.1: water; hydrogenchloride / tetrahydrofuran / 1 h / 50 °C 1.2: 1.67 h / 5 - 25 °C 2.1: methanol; sodium methylate / tetrahydrofuran / 4 h / 20 °C 3.1: sodium hydride / N,N-dimethyl-formamide / 0.5 h / 0 - 5 °C 3.2: 6 h / 0 - 25 °C 4.1: 2,6-dimethylpyridine / acetone / 13 h / 70 °C 5.1: diethylamine; methanol / 3 h / 25 °C 6.1: water; trifluoroacetic acid / 2 h / 25 °C View Scheme | |
Multi-step reaction with 6 steps 1.1: water; hydrogenchloride / tetrahydrofuran / 1 h / 50 °C 1.2: 1.67 h / 5 - 25 °C 2.1: methanol; sodium methylate / tetrahydrofuran / 4 h / 20 °C 3.1: sodium hydride / N,N-dimethyl-formamide / 1 h / 0 - 5 °C 3.2: 3 h / 0 - 25 °C 4.1: 2,6-dimethylpyridine / acetone / 24 h / 70 °C 5.1: diethylamine; methanol / 1 h / 25 °C 6.1: 20% palladium hydroxide-activated charcoal; hydrogen / acetic acid / 2 h / 50 °C View Scheme |
(2S,3S)-4-((1S,2R,3S,4S)-3,4-dihydroxy-2-(hydroxymethyl)tetrahydro-1H-thiophene-1-ium-1-yl)-1,3-dihydroxybutan-2-yl sulfate
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1.1: sodium methylate / tetrahydrofuran; methanol / 4 h / 20 °C 2.1: sodium hydride / N,N-dimethyl-formamide / 0.5 h / 0 - 5 °C 2.2: 6 h / 0 - 25 °C 3.1: 2,6-dimethylpyridine / acetone / 13 h / 70 °C 4.1: diethylamine / methanol / 3 h / 25 °C 5.1: trifluoroacetic acid / water / 2 h / 25 °C View Scheme | |
Multi-step reaction with 5 steps 1.1: sodium methylate / tetrahydrofuran; methanol / 4 h / 20 °C 2.1: sodium hydride / N,N-dimethyl-formamide / 1 h / 0 - 5 °C 2.2: 3 h / 0 - 25 °C 3.1: 2,6-dimethylpyridine / acetone / 24 h / 70 °C 4.1: diethylamine / methanol / 1 h / 25 °C 5.1: hydrogen; acetic acid; 20% palladium hydroxide-activated charcoal / 2 h / 50 °C View Scheme | |
Multi-step reaction with 5 steps 1.1: methanol; sodium methylate / tetrahydrofuran / 4 h / 20 °C 2.1: sodium hydride / N,N-dimethyl-formamide / 0.5 h / 0 - 5 °C 2.2: 6 h / 0 - 25 °C 3.1: 2,6-dimethylpyridine / acetone / 13 h / 70 °C 4.1: diethylamine; methanol / 3 h / 25 °C 5.1: water; trifluoroacetic acid / 2 h / 25 °C View Scheme |
(2S,3S)-4-((1S,2R,3S,4S)-3,4-dihydroxy-2-(hydroxymethyl)tetrahydro-1H-thiophene-1-ium-1-yl)-1,3-dihydroxybutan-2-yl sulfate
Conditions | Yield |
---|---|
Multi-step reaction with 7 steps 1.1: tetrabutyl-ammonium chloride; sodium hydroxide / water; toluene / 3 h / 10 - 25 °C 2.1: hydrogenchloride / tetrahydrofuran; water / 1 h / 50 °C 2.2: 1.67 h / 5 - 25 °C 3.1: sodium methylate / tetrahydrofuran; methanol / 4 h / 20 °C 4.1: sodium hydride / N,N-dimethyl-formamide / 0.5 h / 0 - 5 °C 4.2: 6 h / 0 - 25 °C 5.1: 2,6-dimethylpyridine / acetone / 13 h / 70 °C 6.1: diethylamine / methanol / 3 h / 25 °C 7.1: trifluoroacetic acid / water / 2 h / 25 °C View Scheme | |
Multi-step reaction with 7 steps 1.1: tetrabutyl-ammonium chloride; sodium hydroxide / water; toluene / 3 h / 10 - 25 °C 2.1: hydrogenchloride / tetrahydrofuran; water / 1 h / 50 °C 2.2: 1.67 h / 5 - 25 °C 3.1: sodium methylate / tetrahydrofuran; methanol / 4 h / 20 °C 4.1: sodium hydride / N,N-dimethyl-formamide / 1 h / 0 - 5 °C 4.2: 3 h / 0 - 25 °C 5.1: 2,6-dimethylpyridine / acetone / 24 h / 70 °C 6.1: diethylamine / methanol / 1 h / 25 °C 7.1: hydrogen; acetic acid; 20% palladium hydroxide-activated charcoal / 2 h / 50 °C View Scheme | |
Multi-step reaction with 7 steps 1.1: sodium hydroxide; tetrabutyl-ammonium chloride / water; toluene / 10 °C 1.2: 3 h / 15 - 25 °C 2.1: hydrogenchloride / tetrahydrofuran / 1 h / 50 °C 2.2: 1.5 h / 5 - 25 °C 3.1: sodium methylate / tetrahydrofuran; methanol / 4 h / 20 °C 4.1: sodium hydride / mineral oil; N,N-dimethyl-formamide / 0.5 h / 0 - 5 °C 4.2: 6 h / 0 - 25 °C 5.1: 2,6-dimethylpyridine / acetone / 13 h / 70 °C 6.1: diethylamine / methanol / 3 h / 25 °C 7.1: trifluoroacetic acid / water / 2 h / 25 °C View Scheme | |
Multi-step reaction with 7 steps 1.1: sodium hydroxide; tetrabutyl-ammonium chloride / water; toluene / 10 °C 1.2: 3 h / 15 - 25 °C 2.1: hydrogenchloride / tetrahydrofuran / 1 h / 50 °C 2.2: 1.5 h / 5 - 25 °C 3.1: sodium methylate / tetrahydrofuran; methanol / 4 h / 20 °C 4.1: sodium hydride / mineral oil; N,N-dimethyl-formamide / 1 h / 0 - 5 °C 4.2: 3 h / 0 - 25 °C 5.1: 2,6-dimethylpyridine / acetone / 24 h / 70 °C 6.1: diethylamine / methanol / 1 h / 25 °C 7.1: 20% palladium hydroxide-activated charcoal; hydrogen; acetic acid / 2 h / 50 °C View Scheme |
(2S,3S)-4-((1S,2R,3S,4S)-3,4-dihydroxy-2-(hydroxymethyl)tetrahydro-1H-thiophene-1-ium-1-yl)-1,3-dihydroxybutan-2-yl sulfate
Conditions | Yield |
---|---|
Multi-step reaction with 6 steps 1.1: hydrogenchloride / tetrahydrofuran / 1 h / 50 °C 1.2: 1.5 h / 5 - 25 °C 2.1: sodium methylate / tetrahydrofuran; methanol / 4 h / 20 °C 3.1: sodium hydride / mineral oil; N,N-dimethyl-formamide / 0.5 h / 0 - 5 °C 3.2: 6 h / 0 - 25 °C 4.1: 2,6-dimethylpyridine / acetone / 13 h / 70 °C 5.1: diethylamine / methanol / 3 h / 25 °C 6.1: trifluoroacetic acid / water / 2 h / 25 °C View Scheme | |
Multi-step reaction with 6 steps 1.1: hydrogenchloride / tetrahydrofuran / 1 h / 50 °C 1.2: 1.5 h / 5 - 25 °C 2.1: sodium methylate / tetrahydrofuran; methanol / 4 h / 20 °C 3.1: sodium hydride / mineral oil; N,N-dimethyl-formamide / 1 h / 0 - 5 °C 3.2: 3 h / 0 - 25 °C 4.1: 2,6-dimethylpyridine / acetone / 24 h / 70 °C 5.1: diethylamine / methanol / 1 h / 25 °C 6.1: 20% palladium hydroxide-activated charcoal; hydrogen; acetic acid / 2 h / 50 °C View Scheme |
methanol
(2S,3S)-4-((1S,2R,3S,4S)-3,4-dihydroxy-2-(hydroxymethyl)tetrahydro-1H-thiophene-1-ium-1-yl)-1,3-dihydroxybutan-2-yl sulfate
Conditions | Yield |
---|---|
With hydrogenchloride at 40℃; for 3h; | 93% |
With hydrogenchloride for 1h; Reflux; | 88% |
With hydrogenchloride at 45℃; for 3h; | 86% |
(2S,3S)-4-((1S,2R,3S,4S)-3,4-dihydroxy-2-(hydroxymethyl)tetrahydro-1H-thiophene-1-ium-1-yl)-1,3-dihydroxybutan-2-yl sulfate
(2R,3S,4S)-2-(hydroxymethyl)tetrahydrothiophene-3,4-diol
Conditions | Yield |
---|---|
With NaPMe In methanol for 3h; Heating; | 44% |
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