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(E)-3-(2-pyridyl)propenoic acid hydrochloride | 138643-00-2

中文名称
——
中文别名
——
英文名称
(E)-3-(2-pyridyl)propenoic acid hydrochloride
英文别名
3t-[2]pyridyl-acrylic acid ; hydrochloride;3t-[2]Pyridyl-acrylsaeure; Hydrochlorid;(E)-3-pyridin-2-ylprop-2-enoic acid;hydrochloride
(E)-3-(2-pyridyl)propenoic acid hydrochloride化学式
CAS
138643-00-2
化学式
C8H7NO2*ClH
mdl
——
分子量
185.61
InChiKey
OKWBBAZSMCTWEH-FXRZFVDSSA-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):
    1.6
  • 重原子数:
    12
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    50.2
  • 氢给体数:
    2
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    参考文献:
    名称:
    Structural features of pyridylcinnamic acid dimers and their extended hydrogen-bonded aggregations
    摘要:
    The conformational as well as the structure-forming properties of E-3-(x-pyridyl)propenoic acids (x = 2,3 or 4) have been studied with a combination of computational and spectroscopic methods. IR spectroscopy revealed that in the solid state the zwitterionic species predominate, while NMR measurements showed that dimers, kept together by strong C=O center dot center dot center dot H-O hydrogen bonds, were formed in a dipolar aprotic solvent (DMSO). In concentrated solution, extended aggregation occurred through the cooperative effect of (aromatic) C-H center dot center dot center dot N weak hydrogen bonds. Conformational search was performed at the HF/6-31G(d,p) level of theory. Comparison with experimental values as well as benchmarking calculations at several different levels of theory to probe the performance of the methods, B3LYP/6-31G++(d,p) method was found to be able to provide reasonable geometries as well as quantitative formation energies for the dimers and the tetramers, too. (C) 2014 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.molstruc.2014.11.041
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文献信息

  • Piperidine derivative and use thereof
    申请人:Ikeura Yoshinori
    公开号:US20060142337A1
    公开(公告)日:2006-06-29
    The present invention provides a compound represented by the formula: wherein Ar is an aryl group optionally having substituents, R is a C 1-6 alkyl group, R 1 is a hydrogen atom, a hydrocarbon group optionally having substituents, an acyl group or a heterocyclic group optionally having substituents, X is an oxygen atom or an imino group optionally having substituents, ring A is a piperidine ring optionally further having substituents, and ring B is a benzene ring having substituents, or a salt thereof, and an agent for the prophylaxis or treatment of lower urinary tract abnormality and the like, which contains the compound.
    本发明提供了一种由以下公式表示的化合物: 其中Ar是一个芳基基团,可选地具有取代基,R是一个C1-6烷基基团,R1是一个氢原子,一个可选地具有取代基的烃基团,酰基团或杂环基团,X是一个氧原子或一个可选地具有取代基的亚胺基团,环A是一个哌啶环,可选地进一步具有取代基,环B是一个苯环,具有取代基,或其盐,以及含有该化合物的预防或治疗下尿道异常等的药剂。
  • [EN] NOVEL HETEROCYCLIC ACRYLAMIDES AND THEIR USE AS PHARMACEUTICALS<br/>[FR] NOUVEAUX ACRYLAMIDES HÉTÉROCYCLIQUES ET LEUR UTILISATION EN TANT QUE PRODUITS PHARMACEUTIQUES
    申请人:FAB PHARMA SAS
    公开号:WO2011061214A1
    公开(公告)日:2011-05-26
    The invention relates to novel heterocyclic acrylamide compounds (I), to the preparation of the compounds and intermediates used therein, to the use of the compounds as antibacterial medicaments and pharmaceutical compositions containing the compounds.
    这项发明涉及新颖的杂环丙烯酰胺化合物(I),涉及该化合物及其中间体的制备,涉及将该化合物用作抗菌药物以及含有该化合物的药物组合物的用途。
  • PIPERIDINE DERIVATIVES AND USE THEREOF
    申请人:Takeda Pharmaceutical Company Limited
    公开号:EP1790636A1
    公开(公告)日:2007-05-30
    The present invention provides a compound represented by the formula: wherein Ar is an aryl group optionally having substituents, R is a C1-6 alkyl group, R1 is a hydrogen atom, a hydrocarbon group optionally having substituents, an acyl group or a heterocyclic group optionally having substituents, X is an oxygen atom or an imino group optionally having substituents, ring A is a piperidine ring optionally further having substituents, and ring B is a benzene ring having substituents, or a salt thereof, and an agent for the prophylaxis or treatment of lower urinary tract abnormality and the like, which contains the compound.
    本发明提供了一种由式表示的化合物: 其中 Ar 是任选具有取代基的芳基,R 是 C1-6 烷基,R1 是氢原子、任选具有取代基的烃基、酰基或任选具有取代基的杂环基,X 是氧原子或任选具有取代基的亚基,环 A 是任选进一步具有取代基的哌啶环,环 B 是具有取代基的苯环,或其盐,以及含有该化合物的预防或治疗下尿路异常等疾病的制剂。
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