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【结 构 式】

【分子编号】66781

【品名】5-(1,2-dihydroxyethyl)-3,4-dihydroxydihydrofuran-2(3H)-one

【CA登记号】 

【 分 子 式 】C6H10O6

【 分 子 量 】178.1418

【元素组成】C 40.45% H 5.66% O 53.89%

与该中间体有关的原料药合成路线共 1 条

合成路线1

该中间体在本合成路线中的序号:(I)

 

1 Storer R. Moussa A. Wang JY. Et al. 2005. Synthesis of β-L-2-deoxy-nucleosides from furanoses and pyranoses via a chloro-sugar and anhydro-l-furanosyl-nucleobase intennediatcs as potential antiviral and antineoplastic agents. W0 2005003374
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(X) 62916 {(2S,3R)-5-hydroxy-3-[(4-methylbenzoyl)oxy]tetrahydro-2-furanyl}methyl 4-methylbenzoate C21H22O6 详情 详情
(I) 66781 5-(1,2-dihydroxyethyl)-3,4-dihydroxydihydrofuran-2(3H)-one   C6H10O6 详情 详情
(II) 66782 3-bromo-5-(2-bromo-1-hydroxyethyl)-4-hydroxydihydrofuran-2(3H)-one   C6H8Br2O4 详情 详情
(III) 66783 2,6-dibromo-3,4,5-trihydroxyhexanehydrazide   C6H12Br2N2O4 详情 详情
(IV) 66784 5-(2-bromo-1-hydroxyethyl)-4-hydroxydihydrofuran-2(3H)-one   C6H9BrO4 详情 详情
(V) 66785 potassium 3,4-dihydroxy-4-(oxiran-2-yl)butanoate   C6H9KO5 详情 详情
(VI) 66786 potassium 3-hydroxy-3-(3-(hydroxymethyl)oxiran-2-yl)propanoate   C6H9KO5 详情 详情
(VII) 66787 5-(1,2-dihydroxyethyl)-4-hydroxydihydrofuran-2(3H)-one   C6H10O5 详情 详情
(VIII) 66772 4-hydroxy-5-(hydroxymethyl)dihydrofuran-2(3H)-one   C5H8O4 详情 详情
(IX) 66773     C21H21O6 详情 详情
(XI) 66788 3,5-bis(benzyloxy)-2-((benzyloxy)methyl)tetrahydrofuran   C26H28O4 详情 详情
Extended Information