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3-(3,4-Dihydroxyphenyl)propylamin | 52336-45-5

中文名称
——
中文别名
——
英文名称
3-(3,4-Dihydroxyphenyl)propylamin
英文别名
γ-amino-1,2-dihydroxy-4-propylbenzene;4-(3-Aminopropyl)benzene-1,2-diol
3-(3,4-Dihydroxyphenyl)propylamin化学式
CAS
52336-45-5
化学式
C9H13NO2
mdl
MFCD09744477
分子量
167.208
InChiKey
JDMNLLVJYLMTPE-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):
    -0.6
  • 重原子数:
    12
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.333
  • 拓扑面积:
    66.5
  • 氢给体数:
    3
  • 氢受体数:
    3

文献信息

  • QUINONE CURABLE COMPOSITIONS AND ADHESIVE COMPOSITIONS COMPRISING SAME
    申请人:Kolon Industries, Inc.
    公开号:EP3521372A1
    公开(公告)日:2019-08-07
    The present invention relates to a curable composition and a use thereof and, more particularly, to a curable composition and a use thereof, the curable composition comprising: (a) a compound capable of being denatured to a quinone-based compound by oxygen; (b) an amine-based polymeric compound; and (c) an oxygen clathrate structure. The curable composition is rapidly cured and can be cured not only at an interface of a conventional film but also to the inside of the film, such that the curable composition has uniform physical properties throughout the entire film and excellent physical properties compared to a curing film obtained by curing at an existing interface.
    本发明涉及一种可固化组合物及其用途,更具体地说,涉及一种可固化组合物及其 用途,该可固化组合物包括:(a)一种能被氧气变性为醌基化合物的化合物;(b)一 种胺基高分子化合物;以及(c)一种氧凝胶结构。这种可固化组合物固化速度快,不仅可以在传统薄膜的界面上固化,还可以在薄膜内部固化,因此与在现有界面上固化得到的固化薄膜相比,这种可固化组合物在整个薄膜上具有均匀的物理性能和优异的物理性能。
  • Ecstasy-class derivatives, immunogens, and antibodies and their use in detecting ecstasy-class drugs
    申请人:Roche Diagnostics GmbH
    公开号:EP1498415B1
    公开(公告)日:2007-06-27
  • (METH)ACRYLOYL GROUP-CONTAINING AROMATIC ISOCYANATE COMPOUND AND PRODUCTION PROCESS THEREOF
    申请人:Showa Denko K.K.
    公开号:EP1866357A1
    公开(公告)日:2007-12-19
  • (Meth) Acryloyl Group-Containing Aromatic Isocyanate Compound and Production Process Thereof
    申请人:Nozawa Kaneo
    公开号:US20090054543A1
    公开(公告)日:2009-02-26
    A monomer is provided which is excellent in reactivity, can give high heat resistance and high refractive index, and has two or more polymerizable functional groups with different polymerization properties and an aromatic ring in the molecule. An industrial advantageous process for producing the monomer is also provided. The monomer is an aromatic isocyanate compound containing a (meth)acryloyl group, and is represented by Formula (I): wherein R 1 is a single bond or a linear or branched alkylene group of 1 to 5 carbon atoms, R 2 is a hydrogen atom or a methyl group, R 3 is a single bond or a linear or branched alkylene group of 1 to 3 carbon atoms, X is independently a halogen atom or an electron-withdrawing group, m is an integer ranging from 0 to 4, n is an integer ranging from 1 to 3, and 1≦m+n≦5.
  • Extracts of Curcuma and Methods of Use Thereof
    申请人:Alberte Randall S.
    公开号:US20100098788A1
    公开(公告)日:2010-04-22
    The present invention relates in part to turmeric extracts that are useful for treating or preventing neurodegenerative disorders. Another aspect of the invention relates in part to turmeric extracts that are useful for treating or preventing inflammatory disorders. In some embodiments, the extracts comprise at least one compound selected from the group consisting of 25 to 500 μg bamosamine, 25 to 750 μg echinaxanthol, 100 to 3,000 μg bisdemethoxycurcumin, 50 to 500 μg daphniyunnine E and 500 to 75,000 μg curcumin per 100 mg of extract. Another aspect of the invention relates to pharmaceutical compositions comprising the aforementioned extracts. Another aspect of the invention relates to methods of treating or preventing neurodegenerative disorders comprising administering to a subject in need thereof an effective amount of the aforementioned extracts or compositions. Another aspect of the invention relates to methods of making the aforementioned extracts.
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表征谱图

  • 氢谱
    1HNMR
  • 质谱
    MS
  • 碳谱
    13CNMR
  • 红外
    IR
  • 拉曼
    Raman
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mass
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  • 峰位数据
  • 峰位匹配
  • 表征信息
Shift(ppm)
Intensity
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Assign
Shift(ppm)
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测试频率
样品用量
溶剂
溶剂用量
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