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2-((p-tolyl)methyl)oxirane | 71947-07-4

中文名称
——
中文别名
——
英文名称
2-((p-tolyl)methyl)oxirane
英文别名
2-(4-Methylphenoxy)oxirane
2-((p-tolyl)methyl)oxirane化学式
CAS
71947-07-4
化学式
C9H10O2
mdl
——
分子量
150.177
InChiKey
FCXBYVGEMDNOKS-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:
    11
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    21.8
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    N-benzyl-2-(piperazin-1-yl)acetamide2-((p-tolyl)methyl)oxirane甲醇 为溶剂, 反应 15.0h, 以61.34%的产率得到(R)-N-benzyl-2-(4-(2-hydroxy-3-(p-tolyloxy)propyl)piperazin-1-yl)acetamide
    参考文献:
    名称:
    DERIVATIVES OF 1-PHENOXY PROPAN-2-OL AND PHARMACEUTICAL COMPOSITION CONTAINING THE SAME
    摘要:
    本发明涉及一种新型苯氧丙醇衍生物,其用于阻断T型钙通道和/或TREK通道,以及其用于预防和/或治疗与T型钙通道和/或TREK通道相关的疾病。
    公开号:
    US20150166496A1
  • 作为产物:
    描述:
    参考文献:
    名称:
    Sone, Tomomichi; Isobe, Masakazu; Takabatake, Eigo, Chemical and pharmaceutical bulletin, 1989, vol. 37, # 7, p. 1922 - 1924
    摘要:
    DOI:
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文献信息

  • RING-FUSED 2-PYRIDONE DERIVATIVES AND HERBICIDES
    申请人:Takabe Fumiaki
    公开号:US20110287937A1
    公开(公告)日:2011-11-24
    Provided are 2-pyridone derivatives which have excellent herbicidal activity and exhibit high safety to useful crops and so on; salts thereof; and herbicides containing same. In more detail, 2-pyridone derivatives represented by general formula [I] or agrochemically acceptable salts thereof, and herbicides containing these compounds are provided. In general formula [I], X 1 is an oxygen atom or a sulfur atom; X 2 , X 3 , and X 4 are to each CH or N(O) m ; m is an integer of 0 or 1; R 1 is a hydrogen atom, a C 1-12 alkyl group, or the like; R 2 is a halogen atom, a cyano group, or the like; n is an integer of 0 to 4; R 3 is a hydroxyl group, a halogen atom, or the like; A 1 is C(R 11 R 12 ); A 2 is C(R 13 R 14 ) or C═O; A 3 is C(R 15 R 16 ); and R 11 , R 12 , R 13 , R 14 , R 15 , and R 16 are each independently a hydrogen atom or a C 1-6 alkyl group.
    提供了具有优异除草活性并对有用作物等表现出高安全性的2-吡啶酮衍生物;其盐;以及含有这些化合物的除草剂。更详细地说,提供了通式[I]所表示的2-吡啶酮衍生物或其农药可接受的盐,以及含有这些化合物的除草剂。在通式[I]中,X1是氧原子或硫原子;X2、X3和X4分别为CH或N(O)m;m是0或1的整数;R1是氢原子,C1-12烷基或类似物;R2是卤素原子,氰基或类似物;n是0到4的整数;R3是羟基,卤素原子或类似物;A1是C(R11R12);A2是C(R13R14)或C═O;A3是C(R15R16);R11、R12、R13、R14、R15和R16分别独立地是氢原子或C1-6烷基基团。
  • SONE, TOMOMICHI;ISOBE, MASAKAZU;TAKABATAKE, EIGO, CHEM. AND PHARM. BULL., 37,(1989) N, C. 1922-1924
    作者:SONE, TOMOMICHI、ISOBE, MASAKAZU、TAKABATAKE, EIGO
    DOI:——
    日期:——
  • EPOXY RESIN COMPOSITION, AND, PREPREG AND COPPER CLAD LAMINATE MANUFACTURED USING THE COMPOSITION
    申请人:Shengyi Technology Co., Ltd
    公开号:EP2896653B1
    公开(公告)日:2017-05-31
  • EPOXY RESIN COMPOUND, AND, PREPREG AND COPPER-CLAD LAMINATE MANUFACTURED USING THE COMPOUND
    申请人:Shengyi Technology Co. Ltd.
    公开号:EP2896654B1
    公开(公告)日:2017-07-12
  • EPOXY RESIN COMPOUND AND PREPREG AND COPPER-CLAD LAMINATE MANUFACTURED USING THE COMPOUND
    申请人:Zeng Xianping
    公开号:US20150240055A1
    公开(公告)日:2015-08-27
    The present invention relates to an epoxy resin composition and a prepreg and a copper-clad laminate made by using same. The epoxy resin composition comprises components as follows: an epoxy resin containing 3 or more epoxy groups and containing nitrogen in the molecular chain, a phosphate salt compound and an active ester hardener; the amount of the epoxy resin containing 3 or more epoxy groups and containing nitrogen in the molecular chain is 100 parts by weight, the amount of the phosphate salt compound is 5˜50 parts by weight. The equivalent ratio of the amount of the active ester hardener, based on the ratio between epoxy equivalent and active ester equivalent, is 0.85˜1.2. The prepreg and the copper-clad laminate made by using the epoxy resin composition have excellent dielectric performance, moisture-heat resistant performance, simultaneously have a high glass transition temperature and a lower water absorption rate and simultaneously realize halogen-free flame retardancy, and achieve UL-94V-0.
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