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Cyclopentancarboximidsaeure-methylester-hydrochlorid | 109152-86-5

中文名称
——
中文别名
——
英文名称
Cyclopentancarboximidsaeure-methylester-hydrochlorid
英文别名
cyclopentanecarboximidic acid methyl ester hydrochloride;cyclopentanecarbonimidic acid methyl ester; hydrochloride;Cyclopentancarbimidsaeure-methylester; Hydrochlorid;Cyclopentanecarboximidic acid, methyl ester, hydrochloride;methyl cyclopentanecarboximidate;hydrochloride
Cyclopentancarboximidsaeure-methylester-hydrochlorid化学式
CAS
109152-86-5
化学式
C7H13NO*ClH
mdl
——
分子量
163.647
InChiKey
BTEYJKYYCFVKSU-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):
    2.22
  • 重原子数:
    10
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.86
  • 拓扑面积:
    33.1
  • 氢给体数:
    2
  • 氢受体数:
    2

反应信息

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文献信息

  • [EN] PARTICLES, COMPOSITIONS, AND METHODS FOR OPHTHALMIC AND/OR OTHER APPLICATIONS<br/>[FR] PARTICULES, COMPOSITIONS ET PROCÉDÉS POUR APPLICATIONS OPHTALMIQUES ET/OU AUTRES APPLICATIONS
    申请人:KALA PHARMACEUTICALS INC
    公开号:WO2019055028A1
    公开(公告)日:2019-03-21
    This disclosure relates to particles, compositions, and methods that aid particle transport in mucus are provided. The particles, compositions, and methods may be used, in some instances, for ophthalmic and/or other applications.
    本公开涉及有助于粘液中颗粒传输的颗粒、组合物和方法。这些颗粒、组合物和方法在某些情况下可用于眼科和/或其他应用。
  • Heteroalicyclic carboxamidines as inhibitors of inducible nitric oxide synthase; the identification of (2R)-2-pyrrolidinecarboxamidine as a potent and selective haem-co-ordinating inhibitor
    作者:Robert J. Young、Wendy Alderton、Anthony D.R. Angell、Paul J. Beswick、David Brown、C. Lynn Chambers、Miriam C. Crowe、John Dawson、Christopher C.F. Hamlett、Simon T. Hodgson、Savvas Kleanthous、Richard G. Knowles、Linda J. Russell、Richard Stocker、James M. Woolven
    DOI:10.1016/j.bmcl.2011.03.038
    日期:2011.5
    Heteroalicyclic carboxamidines were synthesised and evaluated as inhibitors of nitric oxide synthases. (2R)-2-Pyrrolidinecarboxamidine, in particular, was shown to be a highly potent in vitro (IC(50) = 0.12 mu M) and selective iNOS inhibitor (> 100-fold vs both eNOS and nNOS), with probable binding to the key anchoring glutamate residue and co-ordination to the haem iron. (C) 2011 Elsevier Ltd. All rights reserved.
  • Gruseck, Ursula; Heuschmann, Manfred, Chemische Berichte, 1987, vol. 120, p. 2053 - 2064
    作者:Gruseck, Ursula、Heuschmann, Manfred
    DOI:——
    日期:——
  • Improved Pinner Reaction with CPME as a Solvent
    作者:Kiyoshi Watanabe、Naoto Kogoshi、Hideaki Miki、Yasuhiro Torisawa
    DOI:10.1080/00397910802632548
    日期:2009.5.7
    The classical Pinner reaction has been improved by the utilization of 4N-HCl solution in cyclopentyl methyl ether (CPME) as a solvent, wherein direct isolation of the product was possible by a simple filtration.
  • McElvain; Starn, Journal of the American Chemical Society, 1955, vol. 77, p. 571,4574
    作者:McElvain、Starn
    DOI:——
    日期:——
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