- 英文名称1-((2R,3R,4R,5R)-5-((Bis(4-Methoxyphenyl)(Phenyl)Methoxy)Methyl)-3-Fluoro-4-Hydroxytetrahydrofuran-2-yl)Pyrimidine-2,4(1H,3H)-Dione
- 中文名称5'-O-DMT-2'-氟-脱氧尿苷
- IUPAC名称1-((2R,3R,4R,5R)-5-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-3-fluoro-4-hydroxytetrahydrofuran-2-yl)pyrimidine-2,4(1H,3H)-dione
- 其它别名2'-Deoxy-5'-O-DMT-2'-fluorouridine
- CAS编号146954-74-7
- MFCD编号:MFCD06657648
- 分子式:C30H29FN2O7
- 分子量:548.56
- 产品CID: 701606
- 产品分类有机原料→生命科学→核苷&核苷酸→DNA亚磷酰胺单体
相似化合物
23669-79-6 103285-22-9 81246-79-9上下游产品
CAS号40615-36-9 4,4'-二甲氧基三苯基氯甲烷 | CAS号146954-75-8 DMT-2′Fluoro-dU...三氯化苄置于aluminum (III) Chloride,Copper(II) Nitrate体系中,用 二氯甲烷 用作溶剂,化学反应 6.0H,反应生成5'-O-[双(4-甲氧基苯基)(苯基)甲基]-2'-脱氧-2'-氟尿苷
参考文献:硝酸铜 (II) 催化区域选择性保护伯醇与核苷和碳水化合物中的 4,4'-二甲氧基三苯甲基和 2,7-二甲基-9-苯基呫吨-9-基
标题:硝酸铜 (II) 催化区域选择性保护伯醇与核苷和碳水化合物中的 4,4'-二甲氧基三苯甲基和 2,7-二甲基-9-苯基呫吨-9-基
摘要:摘要 在作为路易斯酸催化剂的硝酸铜 (II) 存在下,使用二甲氧基三苯甲醇 (Dmtr-Oh) 或二甲基苯甲醇 (Dmpx-Oh) 实现了核苷和碳水化合物类似物中伯羟基的区域选择性保护.观测到优异的选择性保护伯羟基而不是仲羟基,而糖苷键不受影响.通过脂肪族无环和环状二醇的 Dmtr 和 Dmpx 保护进一步举例说明了该方法的实用性.
Doi:10.1080/15257770.2018.1460480
海关参考信息
- 2902300000-甲苯
2905122000-异丙醇
2905310000-1,2-乙二醇
2905320000-1,2-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-10730904-B2
优先权日:2012-11-14
标 题:Method for liquid-phase synthesis of nucleic acid
发明人:NONOGAWA MITSURU; NAGATA TOSHIAKI; SAITO HIDEKI; YASUMA TSUNEO
权利人:TAKEDA PHARMACEUTICALS CO
摘要:In this method, an oligonucleotide represented by formula (II) [wherein Y 1 , Q, Base, r and r′ are each as defined in claim 1 ] is prepared by using, as a synthesis unit, a novel nucleoside monomer compound represented by formula (I) [wherein X, R 1 , Y, Base, Z, Ar, R 2 , R 3 and n are each as defined in claim 1 ]. The novel nucleoside monomer compound is a nucleoside, the base moiety of which is substituted with an aromatic-hydrocarbon-ring-carbonyl or -thiocarbonyl group having at least one hydrophobic group. The method can dispense with column-chromatographic purification in every reaction, and enables base elongation not only in the 3′-direction but also in the 5′-direction, thus attaining efficient liquid-phase mass synthesis of an oligonucleotide.
专利号:US-2019135852-A1
优先权日:2012-11-14
标题 :Method for liquid-phase synthesis of nucleic acid
专利号:EP-2921499-A1
优先权日:2012-11-14
标 题 :Method for liquid-phase synthesis of nucleic acid
专利号:EP-2921499-B1
优先权日:2012-11-14
标 题 :Method for liquid-phase synthesis of nucleic acids
专利号:JP-6218333-B2
优先权日:2012-11-14
标 题 :Method for liquid phase synthesis of nucleic acids
专利号:CN-104918949-B
优先权日:2012-11-14
标 题 :Solution-phase Synthesis of Nucleic Acids