- 英文名称Beta-D-Galactopyranoside, Methyl 1-Thio-, 2,3,4,6-Tetraacetate
- 中文名称甲基 2,3,4,6-O-四乙酰基-β-D-硫代吡喃半乳糖苷
- IUPAC名称(2R,3S,4S,5R,6S)-2-(acetoxymethyl)-6-(methylthio)tetrahydro-2H-pyran-3,4,5-triyl triacetate
- 其它别名Methyl 2,3,4,6-Tetra-O-Acetyl-Beta-D-Thiogalactopyranoside; [(2R,3S,4S,5R,6S)-3,4,5-Triacetyloxy-6-Methylsulfanyloxan-2-Yl]Methyl Acetate; Methyl 2,3,4,6-Tetra-O-Acetyl-; A-D-Thiogalactopyranoside; Xwfuchlbr
- CAS编号55722-48-0
- MFCD编号:MFCD00080806
- 分子式:C15H22O9S分子量:378.4
- 产品CID: 1528712
- 产品分类生物化工 → 糖类化合物 → 单糖

上下游产品
methylthiol 1-bromo-1-deoxy-2,3,4,6-tetra-O-acetyl-a-D-galactopyranoside methyl magnesium iodide 2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl thi°Cyanatemethyl 1-thio-β-D-galactopyranoside Acetic acid (2R,3R,4S,5S,6R)-4,5-diacetoxy-6-acetoxymethyl-2-((2R,3S,4S,5R,6R)-3,4,5,6-tetrakis-benzyloxy-tetrahydro-pyran-2-ylmethoxy)-tetrahydro-pyran-3-yl ester benzyl 6-O-benzyl-3,4-O-isopropylidene-2-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-β-D-galactopyranoside Acetic acid (2S,3R,4S,5S,6R)-4,5-diacetoxy-6-acetoxymethyl-2-((2R,3S,4S,5R,6R)-3,5-bis-benzyloxy-2-benzyloxymethyl-6-methoxy-tetrahydro-pyran-4-yloxy)-tetrahydro-pyran-3-yl ester 📜1-Bromo-2,3,4,6-Tetra-O-Acetyl-D-Galactopyranose置于sodium Acetate体系中,用 丙酮 作为反应溶剂,化学反应 18.0H,反应生成 甲基 2,3,4,6-O-四乙酰基-Beta-D-硫代吡喃半乳糖苷
参考文献:A Through-Process For The Preparation Of Methyl Per-O-Acetyl 1-Thio-Glycosides From Aldoses
标题:A Through-Process For The Preparation Of Methyl Per-O-Acetyl 1-Thio-Glycosides From Aldoses
摘要:D-葡萄糖,D-半乳糖,D-甘露糖,D-木糖,L-阿拉伯糖,L-岩藻糖,L-鼠李糖,麦芽糖,纤维二糖,乳糖,D-葡萄糖胺,D-半乳糖胺和d-甘露糖胺通过一个反应器经过三步(溴乙酰化,甲硫化和乙酰化)转化为相应的甲基全乙酰化1-硫代糖呋喃糖苷.
DOI:10.1246/bcsj.55.3667
海关参考信息
- 2905122000-异丙醇
2905310000-1,2-乙二醇
2905320000-1,2-丙二醇
2905399001-1,3-丙二醇 - 💡 提示:海关信息按照顺序优先匹配,如需确认的海关信息,请参考相关资料。
- 详情请参考:📖 海关编码查询和海关进出口税则
专利信息
专利号:US-2014323705-A1
优先权日:2011-05-13
标题:Manufacture of lacto-n-tetraose
发明人:HEDEROS MARKUS; DEKANY GYULA; DEMKÓ Sà NDOR; Kovács Imre; BAJZA ISTVà N
权利人:HEDEROS MARKUS; DEKANY GYULA; DEMKÓ Sà NDOR; Kovács Imre; BAJZA ISTVà N
摘要:The present invention relates to the synthesis of the tetrasaccharide of formula (I) and novel intermediates used in the synthesis.