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1-beta-D-Arabinofuranosyl-5-iodouracil | CAS:3052-06-0
1-beta-D-Arabinofuranosyl-5-iodouracil
  • 名称:1-beta-D-阿拉伯呋喃糖基-5-碘尿嘧啶 | 1-beta-D-Arabinofuranosyl-5-iodouracil
  • CAS号:3052-06-0
  • 别名:NSC 82221
  • 分子式:C9H11IN2O6
  • 分子量:370.10
  • EINESC号:

产品描述

物理化学性质

熔点 224-226 ºC**
密度 2.27±0.1 g/cm3 (20 ºC

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Calculating virtual log P in the alkane/water system (log P(N)(alk)) and its derived parameters deltalog P(N)(oct-alk) and log D(pH)(alk).Giulia Caron et al.Journal of medicinal chemistry, 48(9), 3269-3279 (2005-04-29) Efficient New Synthesis of N-Arylbenzo [b] furo [3, 2-d] pyrimidin-4-amines and Their Benzo [b] thieno [3, 2-d] pyrimidin-4-amine Analogues via a Microwave-Assisted Dimroth Rearrangement.Loidreau Y, et al. Journal of Heterocyclic Chemistry, 50(5), 1187-1197 (2013) 1, 3-Dipolar Cycloaddition in the Preparation of New Fused Heterocyclic Compounds via Thermal Initiation.Porubsky M, et al. Molecules (Basel), 21(2), 187-187 (2016) Cellular apoptosis and cytotoxicity of phenolic compounds: a quantitative structure-activity relationship study.Cynthia D Selassie et al.Journal of medicinal chemistry, 48(23), 7234-7242 (2005-11-11) Reactivity of 1, 2-cyclic sulfite xylosides towards nucleophiles. Batoux N, et al. Tetrahedron, 65(43), 8858-8862 (2009) Enantioselective Cu-catalyzed 1, 4-addition of Me3Al to a 4, 4-disubstituted cyclohexa-2, 5-dienone.Takemoto Y, et al. Tetrahedron, 52(45), 14177-14188 (1996) Synthesis, Anticonvulsant and Neurotoxicity Evaluation of Some Newer N-(2-benzoylbenzofuran-3-yl)-3-(substituted)-propanamide Analogs.Kamal M, et al. Central Nervous System Agents in Medicinal Chemistry, 13(3), 159-165 (2013) A microwave-assisted multicomponent protocol for the synthesis of benzofuran-2-carboxamides.Vincetti P, et al. Tetrahedron Letters, 57(13), 1464-1467 (2016) meta-Selective arene C-H bond olefination of arylacetic acid using a nitrile-based directing group.Bera M, et al. Organic Letters, 16(21), 5760-5763 (2014) Inhibition of cytochrome P450 3A protein degradation and subsequent increase in enzymatic activity through p38 MAPK activation by acetaminophen and salicylate derivatives.Yuya Ohtsuki et al.Biochemical and biophysical research communications, 509(1), 287-293 (2018-12-28)
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