93635-76-8 (2-C-甲基-4,5-O-(异亚丙基)-D-阿糖酸乙基酯,ethyl (2S,3R)-3-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]-2,3-dihydroxy-2-methylpropanoate)

CAS号:
93635-76-8
中文名称:
2-C-甲基-4,5-O-(异亚丙基)-D-阿糖酸乙基酯
英文名称:
ethyl (2S,3R)-3-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]-2,3-dihydroxy-2-methylpropanoate
分子式:
C11H20O6
分子量:
248.272904396057

2-C-甲基-4,5-O-(异亚丙基)-D-阿糖酸乙基酯(93635-76-8)名称与标识符

名称

中文别名:
(2S,3R)-3-((4R)-2,2-二甲基二氧杂戊环-4-基)-2-甲基-2,3-二羟基丙酸乙酯;5-溴-间苯二甲醇;索非布韦二醇;2-C-甲基-4,5-O-(1-甲基乙烯基)-D-阿拉伯糖酸乙酯;2-C-甲基-4,5-O-(叔 - 亚丁基)-D-阿糖酸乙基酯;2-C-甲基-4,5-O-(异亚丙基)-D-阿糖酸乙基酯;
英文别名:
(2S,3R)-Ethyl 3-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-2,3-dihydroxy-2-methylpropanoate;3-(2,2-Dimethyl-[1,3]dioxolan-4-yl)-2,3-dihydroxy-2-methyl-propionic acid ethyl ester;D-Arabinonic acid, 2-C-methyl-4,5-O-(1-methylethylidene)-,ethyl ester;D-ARABINONIC ACID,2-C-METHYL-4,5-O-(1-METHYLETHYLIDENE)ETHYL ESTER;ethyl (2S,3R)-3-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]-2,3-dihydroxy-2-methylpropanoate;(2S,3R)-3-[(4R)-2,2-dimethyl-[1,3]dioxolan-4-yl]-2,3-dihydroxy-2-methyl-propionic acid ethyl ester;(2S,3R,4R)-4,5-O-isopropylidene-2,3,4,5-tetrahydroxy-2-methyl-pent;2-C-Methyl-4,5-O-(1-methylethylidene)-D-arabinonic acid ethyl ester;D-Arabinonic acid,2-C-methyl-4,5-O-(1-methylethylidene)-,ethyl;ethyl 4,5-O-isopropylidene-2-C-methyl-D-arabinonate;X8443;4,5-O-ISOPROPYLIDENE-2-C-METHYL-D-ARABINONATE;D-ARABINONIC ACID,2-C-METHYL-4,5-O-(1-METHYLETHYLIDENE)-,ETHYL ESTER;D-Arabinonic acid, 2-C-methyl-4,5-O-(1-methylethylidene)-, ethyl ester;(2S,3R)-3-((4R)-2,2-Dimethyldioxolan-4-yl)-2-methyl-2,3-dihydroxypropanoic acid ethyl ester;2-C-Methyl-4,5-O-(1-methylethylidene)-;Ethyl 2-C-methyl-4,5-O-(1-methylethylidene)-D-arabinonate (ACI);D;SCHEMBL768088;AS-19467;(2S,3R)-3-[(4R)-2,2-Dimethyl-[1,3]-dioxolan-4-yl]-2,3-dihydroxy-2-methyl-propionic acid ethyl ester;ethyl (2S,3R)-3-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-2,3-dihydroxy-2-methylpropanoate;MFCD11112138;(2s, 3r)-3-[(4r)-2,2-dimethyl-[1,3]dioxolan-4-yl]-2,3-dihydroxy-2-methyl-propionic acid ethyl ester;C11H20O6;93635-76-8;AKOS022172906;CS-M2472;DTXSID50680992;AC-28966;BHCHXRCKXIVVCN-XLDPMVHQSA-N;D-ARABINONIC ACID,2-C-METHYL-4,5-O-(1-METHYLETHYLIDENE)-,ETHYL ESTER;(2S,3R)-Ethyl 3-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-2,3-dihydroxy-2-methylpropanoate;

标识符

MDL:
MFCD11112138
InChIKey:
BHCHXRCKXIVVCN-XLDPMVHQSA-N
Inchi:
1S/C11H20O6/c1-5-15-9(13)11(4,14)8(12)7-6-16-10(2,3)17-7/h7-8,12,14H,5-6H2,1-4H3/t7-,8-,11+/m1/s1
SMILES:
[C@H]([C@H]1COC(C)(C)O1)(O)[C@@](O)(C)C(=O)OCC

2-C-甲基-4,5-O-(异亚丙基)-D-阿糖酸乙基酯(93635-76-8)物化性质

实验特性

  • LogP : -0.18710
  • PSA : 85.22000
  • 折射率 : 1.475
  • 沸点 : 361.5°C at 760 mmHg
  • 熔点 : 75.0-75.5 ºC
  • 闪点 : 133.189°C
  • 溶解度 : 略溶 (32 g/L) (25 ºC),
  • 密度 : 1.185±0.06 g/cm3 (20 ºC 760 Torr),

计算特性

  • 精确分子量 : 248.12600
  • 氢键供体数量 : 2
  • 氢键受体数量 : 6
  • 可旋转化学键数量 : 5
  • 同位素质量 : 248.126
  • 重原子数量 : 17
  • 复杂度 : 290
  • 同位素原子数量 : 0
  • 确定原子立构中心数量 : 3
  • 不确定原子立构中心数量 : 0
  • 确定化学键立构中心数量 : 0
  • 不确定化学键立构中心数量 : 0
  • 共价键单元数量 : 1
  • 疏水参数计算参考值(XlogP) : -0.3
  • 拓扑分子极性表面积 : 85.2

2-C-甲基-4,5-O-(异亚丙基)-D-阿糖酸乙基酯(93635-76-8)安全信息

2-C-甲基-4,5-O-(异亚丙基)-D-阿糖酸乙基酯(93635-76-8)海关数据

海关编码:
2932999099
海关数据:

中国海关编码:

2932999099

概述:

2932999099. 其他仅含氧杂原子的杂环化合物. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:20.0%

申报要素:

品名, 成分含量, 用途

Summary:

2932999099. other heterocyclic compounds with oxygen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

2-C-甲基-4,5-O-(异亚丙基)-D-阿糖酸乙基酯(93635-76-8)推荐厂家 更多厂家(54)

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上海源叶生物科技有限公司 15026964105
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深圳菲斯生物科技有限公司 18925202235周美娇 2850179284
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北京百灵威科技有限公司 18210857532翟先生 3650742139
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深圳振强生物技术有限公司 13670046396
86-755-66853366
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上海创赛科技有限公司 15021221957
021-59553580
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上海瀚思化工有限公司 18939883912
021-34536277
顾经理 3003949364
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铼博(上海)生化科技有限公司 13311756052
021-60536361 13311756052 13311756131
张经理 2851717387
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上海一基实业有限公司 13311756131
021-60548336 QQ:2355265332 QQ:2851717387
胡经理 2355265332
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上海一基实业有限公司 13311756052
021-60526763 13311756052 13311756131
胡经理 2355265332
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南通众合化工新材料有限公司 18762756250
0513-55074056
胡经理 2369399482
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2-C-甲基-4,5-O-(异亚丙基)-D-阿糖酸乙基酯(93635-76-8)合成路线

合成路线:1 步
反应条件:
参考文献:
Dihydroxylation of Olefins with Potassium Permanganate Catalyzed by Imidazolium Salt
Khan, Imran; Luo, Zhi-Bin ; Valeru, Anil; Xu, Yin; Liu, Bin; et al, Synthesis, 2018, 50(9), 1815-1819
合成路线:1 步
反应条件:
参考文献:
An efficient and practical method for olefin dihydroxylation
Luo, Zhi-bin; Zhao, Chen; Xie, Jimin; Lu, Hong-fei, Synthesis, 2016, 48(21), 3696-3700
合成路线:1 步
反应条件:
参考文献:
Method for preparing ethyl 2-C-methyl-4,5-O-(1-methylethylidene)-D-arabinate
, China, , ,
合成路线:1 步
反应条件:
参考文献:
Preparation of 2'-disubstituted nucleoside and nucleotide triphosphate derivatives and their use as anti-HCV and antiviral agents
, World Intellectual Property Organization, , ,
合成路线:1 步
反应条件:
参考文献:
Preparation of 2'-cyano nucleoside and nucleotide triphosphate derivatives and their use as anti-HCV and antiviral agents
, World Intellectual Property Organization, , ,
合成路线:1 步
反应条件:
参考文献:
Preparation of 2'-substituted nucleoside derivatives and methods of use thereof for the treatment of viral diseases
, World Intellectual Property Organization, , ,
合成路线:1 步
反应条件:
参考文献:
Preparation method of intermediate of sofosbuvir
, China, , ,
合成路线:1 步
反应条件:
参考文献:
Preparation of 2'-cyano substituted nucleoside derivatives and methods of use thereof for the treatment of viral diseases
, Canada, , ,
合成路线:1 步
反应条件:
参考文献:
Bi- and monocyclic nucleoside analogs for treatment of hepatitis e
, World Intellectual Property Organization, , ,
合成路线:1 步
反应条件:
参考文献:
Preparation of substituted nucleosides, nucleotides and analogs thereof as antitumor and HCV antiviral agents
, World Intellectual Property Organization, , ,
合成路线:1 步
反应条件:
参考文献:
prepn of substituted nucleosides, nucleotides and analogs thereof as antiviral agents
, United States, , ,
合成路线:1 步
反应条件:
参考文献:
Preparation of substituted nucleosides, nucleotides and analogs thereof as antiviral agents
, World Intellectual Property Organization, , ,
合成路线:1 步
反应条件:
参考文献:
Process for preparation of 3,5-dibenzoyl-2-deoxy-2-fluoro-2-methyl-D-ribose-γ-lactone
, China, , ,
合成路线:1 步
参考文献:
Improved synthesis method of sofosbuvir drug for treatment of hepatitis C by using sodium permanganate oxidizer, tin tetrachloride catalyst and pentafluorophenol
, China, , ,
合成路线:1 步
参考文献:
2'-cyano substituted nucleoside derivatives and methods of use thereof for the treatment of viral diseases
, United States, , ,
合成路线:1 步
参考文献:
Preparation of alkyl-substituted 2-deoxy-2-fluoro-D-ribofuranosyl pyrimidine and purine nucleoside analogs via condensation of the lactone to nucleosides as potential antiviral agents
, World Intellectual Property Organization, , ,
合成路线:1 步
参考文献:
Branched-chain sugars, part VII. Synthesis of saccharinic acid derivatives
Lopez Aparicio, Fidel J.; Izquierdo Cubero, Isidoro; Portal Olea, Maria D., Carbohydrate Research, 1984, 129, 99-109

2-C-甲基-4,5-O-(异亚丙基)-D-阿糖酸乙基酯(93635-76-8)上下游