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2-(5-Methyl-2-benzofuranyl)benzonitrile | 143381-79-7

中文名称
——
中文别名
——
英文名称
2-(5-Methyl-2-benzofuranyl)benzonitrile
英文别名
2-(2'-cyanophenyl)-5-methylbenzofuran;2-(5-Methylbenzofuran-2-yl)benzonitrile;2-(5-methyl-1-benzofuran-2-yl)benzonitrile
2-(5-Methyl-2-benzofuranyl)benzonitrile化学式
CAS
143381-79-7
化学式
C16H11NO
mdl
——
分子量
233.269
InChiKey
OACAGQBRVQSDKA-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):
    4.1
  • 重原子数:
    18
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    36.9
  • 氢给体数:
    0
  • 氢受体数:
    2

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • Benzo-fused lactams promote release of growth hormone
    申请人:Merck & Co., Inc.
    公开号:US05374721A1
    公开(公告)日:1994-12-20
    There are disclosed certain novel compounds identified as benzo-fused lactams which promote the release of growth hormone in humans and animals. This property can be utilized to promote the growth of food animals to render the production of edible meat products more efficient, and in humans, to increase the stature of those afflicted with a lack of a normal secretion of natural growth hormone. Growth promoting compositions containing such benzo-fused lactams as the active ingredient thereof are also disclosed.
    已披露了某些新型化合物,被识别为苯并融合内酰胺,能促进人类和动物体内生长激素的释放。这种特性可以用于促进食用动物的生长,使可食肉制品的生产更加高效,在人类中,可以增加那些因缺乏正常分泌天然生长激素而受影响的人的身高。还披露了含有这些苯并融合内酰胺作为活性成分的促生长组合物。
  • N-acyl-n-quinolinyl or isoquinounyl alkylamino acids compositions and
    申请人:Ciba-Geigy Corporation
    公开号:US05506240A1
    公开(公告)日:1996-04-09
    The invention relates to N-acyl-N-heterocyclylalkylamino acids of the formula ##STR1## The compounds and their pharmaceutically acceptable salts can be used as antihypertensives, agents for the treatment of glaucoma, or for increasing the flow of the retinal ocular fluid.
    该发明涉及公式为N-acyl-N-杂环烷基氨基酸的化合物。这些化合物及其药用盐可用作降压药、治疗青光眼的药物,或用于增加视网膜眼液的流动。
  • Pyrazole containing benzofuran derivatives and pharmaceutical
    申请人:Glaxo Group Limited
    公开号:US05252593A1
    公开(公告)日:1993-10-12
    The invention provides compounds of formula (I): ##STR1## or a physiologically acceptable salt, solvate or metabolically labile ester thereof. The compounds may be used in the treatment or prophylaxis of hypertension and diseases associated with cognitive disorders.
    该发明提供了式(I)的化合物:##STR1## 或其生理上可接受的盐,溶剂或代谢不稳定的酯。这些化合物可用于治疗或预防高血压和与认知障碍相关的疾病。
  • Benzofuran derivatives
    申请人:Glaxo Group
    公开号:US05498722A1
    公开(公告)日:1996-03-12
    The invention provides compounds of formula (I): ##STR1## or a physiologically acceptable salt, solvate or metabolically labile ester thereof wherein the R groups are defined in the specification. The compounds may be used in the treatment or prophylaxis of hypertension and diseases associated with cognitive disorders.
    该发明提供了式(I)的化合物:##STR1##或其生理上可接受的盐、溶剂或代谢易降解的酯,其中R基在说明书中定义。这些化合物可用于治疗或预防高血压和与认知障碍相关的疾病。
  • N-Imidazolylmethyl benzofuran derivatives as inhibitors of angiotensin II activity
    申请人:GLAXO GROUP LIMITED
    公开号:EP0505954A1
    公开(公告)日:1992-09-30
    The invention provides compounds of the general formula (I): or a physiologically acceptable salt, solvate or metabolically labile ester thereof wherein R¹ represents a hydrogen atom or a halogen atom or a group selected from C₁₋₆alkyl, C₂₋₆alkenyl, fluoroC₁₋₆alkyl, C₁₋₆alkoxy ,-CHO, -CO₂H or -COR²; Ar represents the group R² represents a group selected from C₁₋₆alkyl, C₂₋₆alkenyl, C₁₋₆alkoxy or the group -NR¹²R¹³; R³ represents a group selected from -CO₂H, -NHSO₂CF₃ or a C-linked tetrazolyl group; R⁴ and R⁵ which may be the same or different each independently represent a hydrogen atom or a halogen atom or a C₁₋₆alkyl group; Het represents the group R⁶ represents a hydrogen atom or a group selected from C₁₋₆alkyl, C₂₋₆alkenyl, C₁₋₆alkylthio, C₁₋₆alkoxy, C₃₋₇cycloalkyl or C₃₋₇cycloalkylC₁₋₄alkyl; R⁷ represents a hydrogen atom or a halogen atom or a group selected from C₁₋₆alkyl, C₂₋₆alkenyl or fluoroC₁₋₆alkyl; R⁸ represents a hydrogen atom or a C₁₋₆alkyl group; R⁹ represents a hydrogen atom or a group selected from phenyl or C₁₋₆alkyl, optionally substituted by a phenyl, hydroxyphenyl, hydroxyl, amino, guanidino, imidazolyl, indolyl, mercapto, C₁₋₆alkylthio, carboxyl or amido group; or R⁸ and R⁹, when taken together, form an alkylene bridge of 2, 3 or 4 carbon atoms; R¹⁰ represents a hydrogen atom or a C₁₋₆alkyl group; R¹¹ represents a group selected from hydroxyl, C₁₋₆alkoxy, C₂₋₆alkenoxy or -NR¹²R¹³; R¹² and R¹³, which may be the same or different, each independently represent a hydrogen atom or a C₁₋₄alkyl group or -NR¹²R¹³ forms a saturated heterocyclic ring which has 5 or 6 ring members and may optionally contain in the ring one oxygen atom; m represents zero or an integer from 1 to 4; and n represents zero or an integer from 1 to 3; with the proviso that when n represents an integer from 1 to 3, R⁹ and R¹⁰ both represent hydrogen atoms. The compounds may be used in the treatment or prophylaxis of hypertension and diseases associated with cognitive disorders.
    本发明提供通式 (I) 的化合物: 或其生理上可接受的盐、溶解物或代谢易变酯 其中 R¹ 代表氢原子或卤素原子或选自 C₁₋₆ 烷基、C₂₋₆烯基、氟 C₁₋₆ 烷基、C₁₋₆ 烷氧基、-CHO、-CO₂H 或 -COR² 的基团; Ar 代表以下基团 R² 代表选自 C₁₋₆烷基、C₂₋₆烯基、C₁₋₆烷氧基或 -NR¹²R¹³ 的基团; R³ 代表选自-CO₂H、-NHSO₂CF₃或 C-连环四唑基的基团; R⁴ 和 R⁵ 可以相同或不同,各自独立地代表氢原子、卤素原子或 C₁₋₆ 烷基; Het 代表以下基团 R⁶ 代表氢原子或选自 C₁₋₆烷基、C₂₋₆烯基、C₁₋₆烷硫基、C₁₋₆烷氧基、C₃₋₇cycloalkylC₁₋₄烷基的基团; R⁷ 代表氢原子或卤原子或选自 C₁₋₆烷基、C₂₋₆烯基或氟 C₁₋₆烷基的基团; R⁸ 代表氢原子或 C₁₋₆ 烷基; R⁹ 代表氢原子或选自苯基或 C₁₋₆烷基的基团,可选择被苯基、羟基苯基、羟基、氨基、胍基、咪唑基、吲哚基、巯基、C₁₋₆烷硫基、羧基或氨基取代;或 R⁸ 和 R𠞙 结合在一起时,形成 2、3 或 4 个碳原子的亚烷基桥; R¹⁰ 代表氢原子或 C₁₋₆ 烷基; R¹¹ 代表选自羟基、C₁₋₆烷氧基、C₂₋₆烯氧基或 -NR¹²R¹³ 的基团; R¹²和 R¹³可以相同或不同,各自独立地代表氢原子或 C₁₋₄烷基或 -NR¹²R¹³ 形成饱和杂环,该杂环有 5 或 6 个环成员,环中可任选含有一个氧原子; m 代表零或 1 至 4 的整数;以及 n 代表零或 1 至 3 的整数;但当 n 代表 1 至 3 的整数时,R⁹ 和 R¹⁰ 均代表氢原子。 这些化合物可用于治疗或预防高血压和与认知障碍有关的疾病。
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