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5-氯甲基尿苷 | 89148-09-4

中文名称
5-氯甲基尿苷
中文别名
——
英文名称
5-chloromethyluridine
英文别名
1-[(3aR,4R,6R,6aR)-6-(hydroxymethyl)-2,2-dimethyl-3a,4,6,6a-tetrahydrofuro[3,4-d][1,3]dioxol-4-yl]-5-(chloromethyl)pyrimidine-2,4-dione
5-氯甲基尿苷化学式
CAS
89148-09-4
化学式
C13H17ClN2O6
mdl
——
分子量
332.741
InChiKey
UMLWWHFTCFOBQD-TURQNECASA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 密度:
    1.403±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -0.9
  • 重原子数:
    22
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.69
  • 拓扑面积:
    97.3
  • 氢给体数:
    2
  • 氢受体数:
    6

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    参考文献:
    名称:
    修饰的核苷从tRNA的“摆动位置”开始。5-羧甲基氨基甲基尿苷和5-羧甲基氨基甲基-2-硫尿苷的合成
    摘要:
    已经描述了从tRNA 1 Gly(枯草芽孢杆菌)分离的5-羧甲基氨基甲基尿苷及其从tRNA Lys(枯草芽孢杆菌)的2-硫类似物的合成。
    DOI:
    10.1016/s0040-4039(00)87878-8
  • 作为产物:
    描述:
    参考文献:
    名称:
    Synthesis and Properties of Conformationally Rigid Cyclouridylic Acids Having Covalent Bonding Linkers Between the Uracil 5-Position and the 5′-Phosphate Group
    摘要:
    Conformationally rigid cyclouridylic acid derivatives 2 and 3 having ethylene and propylene bridges, respectively, between the uracil 5-position and the 5'-phosphate group were synthesized. These intramolecularly cyclized compounds have predominantly the ribose pucker of C3'-endo and the g+ orientation around the C4'-C5' bond.
    DOI:
    10.1080/07328319708006125
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文献信息

  • mt-tRNA Components: Synthesis of (2-Thio)Uridines Modified with Blocked Glycine/Taurine Moieties at C-5,1
    作者:Grazyna Leszczynska、Piotr Leonczak、Agnieszka Dziergowska、Andrzej Malkiewicz
    DOI:10.1080/15257770.2013.838261
    日期:2013.11.2
    5-carboxymethylaminomethyl(-2-thio)uridine (cmnm5(s2)U) and 5-taurinomethyl(-2-thio)uridine (τm5(s2)U) with a blocked amino acid function. 2-(Trimethylsilyl)ethyl and 2-(p-nitrophenyl)ethyl esters of glycine and 2-(2,4,5-trifluorophenyl)ethyl ester of taurine were selected as protection of carboxylic and sulfonic acid residues, respectively. The first synthesis of 5-formyl-2′,3′-O-isopropylidene-2-thiouridine
    在本文中,我们讨论了在三乙酰氧基硼氢化钠(NaBH(OAc)3)存在下,用甘酸或牛磺酸酯对5-甲酰基-2',3'-O-异亚丙基(-2-基)尿苷进行基化还原胺化的有用性。用于合成天然线粒体(mt)tRNA组分5-羧甲基氨基甲基(-2-代)尿苷(cmnm5(s2)U)和5-牛磺基甲基(-2-代)尿苷(τm5(s2)U)氨基酸功能。分别选择甘酸的2-(三甲基甲硅烷基)乙酯和2-(对硝基苯基)乙酯牛磺酸的2-(2,4,5-三氟苯基)乙酯作为羧酸磺酸残基的保护剂。还报道了5-甲酰基-2',3'-O-异亚丙基-2-尿苷的首次合成。
  • Malkiewicz, Andrzej J.; Nawrot, Barbara; Sochacka, Elzbieta, Zeitschrift fur Naturforschung, B: Chemical Sciences, 1987, vol. 42, # 3, p. 360 - 366
    作者:Malkiewicz, Andrzej J.、Nawrot, Barbara、Sochacka, Elzbieta
    DOI:——
    日期:——
  • Chemical Synthesis and Properties of 5-Taurinomethyluridine and 5-Taurinomethyl-2-thiouridine
    作者:Toshihiko Ogata、Tomomi Shimazaki、Tadashi Umemoto、Shinya Kurata、Takashi Ohtsuki、Tsutomu Suzuki、Takeshi Wada
    DOI:10.1021/jo802697r
    日期:2009.3.20
    Unique taurine-containing Uridine derivatives, 5-taurinomethyluridine (tau m(5)U) and 5-taurinomethyl-2-thiouridine (tau m(5)s(2)U), which were discovered in mammalian mitochondrial tRNAs, exist at the first position of the anticodon. In this paper, we report the first efficient synthesis of tau m(5)U and tau m(5)s(2)U and describe their physicochemical properties. These modified ribonucleosides were synthesized by the reaction of 5-substituted uridine derivatives with a tetrabutylammonium salt of taurine that is highly reactive and well-soluble in common organic solvents. UV and H-1 NMR spectrometric studies revealed the structural properties of the taurine-containing base moieties and the Sugar conformations of these modified ribonucleosides.
  • Sekine; Seio; Wada, Journal of the American Chemical Society, 1994, vol. 116, # 10, p. 4469 - 4470
    作者:Sekine、Seio、Wada、Sakamoto、Yokoyama
    DOI:——
    日期:——
  • Ahmed, A. F. Sayed, Journal of Chemical Research, Miniprint, 1998, # 11, p. 3011 - 3018
    作者:Ahmed, A. F. Sayed
    DOI:——
    日期:——
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