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3-(溴甲基)-2,6-二甲氧基吡啶 | 934286-66-5

中文名称
3-(溴甲基)-2,6-二甲氧基吡啶
中文别名
——
英文名称
3-(Bromomethyl)-2,6-dimethoxypyridine
英文别名
——
3-(溴甲基)-2,6-二甲氧基吡啶化学式
CAS
934286-66-5
化学式
C8H10BrNO2
mdl
——
分子量
232.077
InChiKey
CGZARUONTNTXET-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):
    2
  • 重原子数:
    12
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    31.4
  • 氢给体数:
    0
  • 氢受体数:
    3

安全信息

  • 海关编码:
    2933399090

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

反应信息

  • 作为反应物:
    描述:
    3-(溴甲基)-2,6-二甲氧基吡啶 在 sodium hydride 作用下, 以 二氯甲烷甲苯 为溶剂, 反应 20.0h, 生成 (Z)-3-(3-((tert-butyldimethylsilyl)oxy)-4-methoxystyryl)-2,6-dimethoxypyridine
    参考文献:
    名称:
    Novel pyridinyl and pyrimidinylcarbazole sulfonamides as antiproliferative agents
    摘要:
    A series of azaheterocyclic carbazole sulfonamides was synthesized and evaluated for antiproliferative activity. The most potent compounds N-(2,6-dimethoxypyridine-3-yl)-9-ethyl and 9-methylcarbazole-3-sulfonamide (13 and 14) gave significant cytotoxicity (IC50 = 122 and 101 nM). Compound 13 displayed submicromolar activities against seven human tumor cell lines. The SARs of this series of sulfonamides which includes the influence of azaheterocycle rings, sulfonamide linkage, and the carbazole ring are described.
    DOI:
    10.1016/j.bmcl.2006.12.034
  • 作为产物:
    描述:
    3-溴-2,6-二甲氧基吡啶 在 sodium tetrahydroborate 、 正丁基锂三溴化磷 作用下, 以 四氢呋喃甲醇二氯甲烷 为溶剂, 反应 17.0h, 生成 3-(溴甲基)-2,6-二甲氧基吡啶
    参考文献:
    名称:
    Novel pyridinyl and pyrimidinylcarbazole sulfonamides as antiproliferative agents
    摘要:
    A series of azaheterocyclic carbazole sulfonamides was synthesized and evaluated for antiproliferative activity. The most potent compounds N-(2,6-dimethoxypyridine-3-yl)-9-ethyl and 9-methylcarbazole-3-sulfonamide (13 and 14) gave significant cytotoxicity (IC50 = 122 and 101 nM). Compound 13 displayed submicromolar activities against seven human tumor cell lines. The SARs of this series of sulfonamides which includes the influence of azaheterocycle rings, sulfonamide linkage, and the carbazole ring are described.
    DOI:
    10.1016/j.bmcl.2006.12.034
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文献信息

  • Novel pyridinyl and pyrimidinylcarbazole sulfonamides as antiproliferative agents
    作者:Laixing Hu、Zhuo-rong Li、Yue-ming Wang、Yanbin Wu、Jian-Dong Jiang、David W. Boykin
    DOI:10.1016/j.bmcl.2006.12.034
    日期:2007.3
    A series of azaheterocyclic carbazole sulfonamides was synthesized and evaluated for antiproliferative activity. The most potent compounds N-(2,6-dimethoxypyridine-3-yl)-9-ethyl and 9-methylcarbazole-3-sulfonamide (13 and 14) gave significant cytotoxicity (IC50 = 122 and 101 nM). Compound 13 displayed submicromolar activities against seven human tumor cell lines. The SARs of this series of sulfonamides which includes the influence of azaheterocycle rings, sulfonamide linkage, and the carbazole ring are described.
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