CAS: 4330-21-6; (2R,3S,5R)-5-Chloro-2-(((4-Methylbenzoyl)Oxy)Methyl)Tetrahydrofuran-3-Yl 4-Methylbenzoate

相似化合物

3601-89-6 21740-23-8 3601-90-9

上下游产品

CAS号4330-34-1 1-甲氧基-2-脱氧-3,5-... | CAS号78185-64-5 methyl 2-deoxy-... | CAS号452-51-7 2-deoxy-D-ribof... | CAS号874-60-2 对甲基苯甲酰氯 | CAS号78185-65-6 methyl 2-deoxy-... | CAS号13222-85-0 对甲苯甲酸酐 | CAS号4291-63-8 克拉利宾 | CAS号60129-59-1 7-Deaza-2'-脱氧腺苷 | CAS号143632-16-0 1-(2-deoxyribof... | CAS号92233-50-6 Aids186752 | CAS号91713-46-1 6-氯-9-(2'-脱氧-3'... | CAS号91713-51-8 3,5-O-Ditoluoyl... | CAS号34371-14-7 (4S,5R)-4-羟基-5-... | CAS号958-09-8 2'-脱氧腺苷 | CAS号29900-44-5 2'-deoxy-3',5'-...

5-(Hydroxymethyl)Oxolane-2,4-Diol,对甲基苯甲酰氯置于乙酰氯,4-二甲氨基吡啶体系中,用 甲醇,吡啶 作为反应溶剂,化学反应 1.0H,以69%的收率获得产物1-氯-3,5-二-O-对甲苯甲酰基-2-脱氧-D-呋喃核糖
参考文献:一种苯并咪唑衍生物bi277及其制备方法和应用
标题:一种苯并咪唑衍生物bi277及其制备方法和应用
摘要:本发明公开了一种苯并咪唑衍生物bi277及其制备方法,其化学命名为1‑[四氢‑4‑羟基‑5‑(羟甲基)呋喃‑2‑基]‑1H‑苯并[d]咪唑‑4‑甲酰胺.本发明的苯并咪唑衍生物及其药学上可接受的盐,溶剂化物和水合物对mcf‑7,Sk‑br‑3,Hct 116,U‑118 Mg,U‑87 Mg,Mda‑mb‑468具有优秀的抗肿瘤体内外活性,在制备抗肿瘤药物的上具有较好的应用前景.

专利信息

专利号:US-7759469-B2
优先权日:2005-03-10
标 题 :Labeling reagent
发明人：HEINDL DIETER; FROEHLICH THOMAS; MAERZ HERIBERT; SELLER MONIKA
权利人:ROCHE DIAGNOSTICS OPERATIONS
摘要:The current invention restates substituted nitroindole nucleosides as both terminal as well as internal building blocks of labeled oligonucleotide probes for the detection, analysis and quantitation of nucleic acids. The substituent comprises a linker and a detectable group or a linker and a reactive group for post synthesis coupling. These modified nucleosides grant access to a wide application area. These new substituted nitroindole nucleosides can be used as labeling reagents for the facile preparation of, e.g., optimized hybridization probes, simple probes, TAQMAN-probes or molecular beacon probes.

专利号:US-7759470-B2
优先权日:2006-02-20
标 题 :Labeling reagent
发明人：HEINDL DIETER; BERGMANN FRANK; JOSEL HANS-PETER; KESSLER DIRK; LAMPERT GUNTER; WEILKE CHRISTIAN
权利人:ROCHE DIAGNOSTICS OPERATIONS
摘要:The current invention restates substituted indole nucleosides as both terminal as well as internal building blocks of labeled oligonucleotide probes for the detection, analysis and quantitation of nucleic acids. The substituent comprises a linker and a detectable group or a linker and a reactive group for post synthesis coupling. These modified nucleosides grant access to a wide application area. These new substituted indole nucleosides can be used as labeling reagents for the facile preparation of e.g. optimized hybridization probes, Taqman-probes, or molecular beacon probes.