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methyl 2-hydroxy-2-methyl-3-(phenylthio)propanoate

中文名称
——
中文别名
——
英文名称
methyl 2-hydroxy-2-methyl-3-(phenylthio)propanoate
英文别名
Methyl 2-hydroxy-2-methyl-3-phenylsulfanylpropanoate
methyl 2-hydroxy-2-methyl-3-(phenylthio)propanoate化学式
CAS
——
化学式
C11H14O3S
mdl
——
分子量
226.296
InChiKey
FTTGFIFPWAJUAD-UHFFFAOYSA-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

计算性质

  • 辛醇/水分配系数(LogP):
    1.9
  • 重原子数:
    15
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.36
  • 拓扑面积:
    71.8
  • 氢给体数:
    1
  • 氢受体数:
    4

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:
    描述:
    参考文献:
    名称:
    1,2,4-Oxadiazoles: A new class of anti-prostate cancer agents
    摘要:
    Sulfide and sulfonyl derivatives of 1,2,4-oxadiazoles were synthesized and screened by MTT assay on the prostate cancer cells, DU-145. Six compounds were identified as potential anti-prostate cancer agents with IC50 values ranging from 0.5 to 5.1 mu M. These compounds exhibited good activity on the androgen independent cells PC-3, while the results were moderate on androgen dependent LNCaP cells, suggesting the possibility of a mechanism of action different from that of the bioisosteric bicalutamide. Also a very low cytotoxicity was observed on non-cancerous cells MCF-10A. (c) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2012.01.059
  • 作为产物:
    描述:
    甲基丙烯酸甲酯Oxonepotassium carbonate 、 potassium hydroxide 作用下, 以 甲醇乙腈 为溶剂, 生成 methyl 2-hydroxy-2-methyl-3-(phenylthio)propanoate
    参考文献:
    名称:
    1,2,4-Oxadiazoles: A new class of anti-prostate cancer agents
    摘要:
    Sulfide and sulfonyl derivatives of 1,2,4-oxadiazoles were synthesized and screened by MTT assay on the prostate cancer cells, DU-145. Six compounds were identified as potential anti-prostate cancer agents with IC50 values ranging from 0.5 to 5.1 mu M. These compounds exhibited good activity on the androgen independent cells PC-3, while the results were moderate on androgen dependent LNCaP cells, suggesting the possibility of a mechanism of action different from that of the bioisosteric bicalutamide. Also a very low cytotoxicity was observed on non-cancerous cells MCF-10A. (c) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2012.01.059
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文献信息

  • Auto-oxidative hydroxysulfenylation of alkenes
    作者:Congde Huo、Yajun Wang、Yong Yuan、Fengjuan Chen、Jing Tang
    DOI:10.1039/c6cc01937d
    日期:——

    One-pot auto-oxidation mediated hydroxysulfenylation of electron-deficient and electron-rich olefins with phenthiols was explored.

    一锅法介导的电子不足和电子富集烯烃与苯硫醇的羟基硫醚化反应被探索。
  • Hydroxysulfenylation of Electron-Deficient Alkenes through an Aerobic Copper Catalysis
    作者:Hui Xi、Bicheng Deng、Zhenzhen Zong、Shenglin Lu、Zhiping Li
    DOI:10.1021/acs.orglett.5b00112
    日期:2015.3.6
    A copper-catalyzed hydroxysulfenylation of α,β-unsaturated esters/amides is reported. The method presents a selective and efficient synthesis of β-hydroxysulfides bearing electron-withdrawing groups. The synthetic utility of this method is demonstrated by the concise synthesis of the anticancer drug bicalutamide.
    据报道,铜催化的α,β-不饱和酯/酰胺的羟基亚磺酰基化。该方法提出了具有吸电子基团的β-羟基硫化物的选择性和有效的合成。该方法的合成效用通过抗癌药物比卡鲁胺的简明合成得到证明。
  • Bredereck,H. et al., Chemische Berichte, 1960, vol. 93, p. 2415 - 2423
    作者:Bredereck,H. et al.
    DOI:——
    日期:——
  • 1,2,4-Oxadiazoles: A new class of anti-prostate cancer agents
    作者:Gopal L. Khatik、Jasmine Kaur、Varun Kumar、Kulbhushan Tikoo、Vipin A. Nair
    DOI:10.1016/j.bmcl.2012.01.059
    日期:2012.3
    Sulfide and sulfonyl derivatives of 1,2,4-oxadiazoles were synthesized and screened by MTT assay on the prostate cancer cells, DU-145. Six compounds were identified as potential anti-prostate cancer agents with IC50 values ranging from 0.5 to 5.1 mu M. These compounds exhibited good activity on the androgen independent cells PC-3, while the results were moderate on androgen dependent LNCaP cells, suggesting the possibility of a mechanism of action different from that of the bioisosteric bicalutamide. Also a very low cytotoxicity was observed on non-cancerous cells MCF-10A. (c) 2012 Elsevier Ltd. All rights reserved.
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