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【结 构 式】

【分子编号】66254

【品名】(3S,5S)-2-(hydroxymethyl)-5-methoxytetrahydrofuran-3-ol

【CA登记号】 

【 分 子 式 】C6H12O4

【 分 子 量 】148.15888

【元素组成】C 48.64% H 8.16% O 43.2%

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 BerrHattar J, Jiricny J. 1986. An improved syntbesis of 2'-deoxy5-azacytidine by condensation of an 9-flu-orenylmethoxycarbonyl-protected sug:ar onto the silylated base. J Org Chem, 51r 3211 --3213
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 66254 (3S,5S)-2-(hydroxymethyl)-5-methoxytetrahydrofuran-3-ol   C6H12O4 详情 详情
(II) 66255 ((2S,4S)-2-((((9H-fluoren-9-yl)peroxy)carbonyl)oxy)-4-methoxycyclopentyl)methyl 9H-fluoren-9-yl carbonoperoxoate   C35H30O9 详情 详情
(III) 66256 ((1R,4R)-2-((((9H-fluoren-9-yl)peroxy)carbonyl)oxy)-4-chlorocyclopentyl)methyl 9H-fluoren-9-yl carbonoperoxoate   C34H27ClO8 详情 详情
(IV) 11626 N-(Trimethylsilyl)-4-[(trimethylsilyl)oxy]-1,3,5-triazin-2-amine; N-(Trimethylsilyl)-N-[4-[(trimethylsilyl)oxy]-1,3,5-triazin-2-yl]amine C9H20N4OSi2 详情 详情
(V) 66257 ((2R,4R)-2-((((9H-fluoren-9-yl)peroxy)carbonyl)oxy)-4-(4-amino-2-oxo-1,3,5-triazin-1(2H)-yl)cyclopentyl)methyl 9H-fluoren-9-yl carbonoperoxoate   C37H30N4O9 详情 详情
(VI) 66142     C37H30N4O9 详情 详情
Extended Information