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6-Hexoxynaphthalene-2-carboxylic acid;hydrochloride

中文名称
——
中文别名
——
英文名称
6-Hexoxynaphthalene-2-carboxylic acid;hydrochloride
英文别名
6-hexoxynaphthalene-2-carboxylic acid;hydrochloride
6-Hexoxynaphthalene-2-carboxylic acid;hydrochloride化学式
CAS
——
化学式
C17H21ClO3
mdl
——
分子量
308.8
InChiKey
RNQKVUDELAOAIF-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):
    4.92
  • 重原子数:
    21
  • 可旋转键数:
    7
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.35
  • 拓扑面积:
    46.5
  • 氢给体数:
    2
  • 氢受体数:
    3

文献信息

  • SUBSTITUTED AMINO ALCOHOLS AS CHIRAL DOPANTS
    申请人:Fraunhofer-Gesellschaft zur Förderung der Angewandten Forschung E.V.
    公开号:US20140228591A1
    公开(公告)日:2014-08-14
    The invention relates to the use of a substituted, chiral amino alcohol, comprising one or more structural units of the following formula (1), wherein the abbreviations A, Y, R1 and R3 to R5 have the following meanings: is a covalent bond or a hydrocarbon group, Y is a covalent bond or a hydrocarbon group that can have an oxygen atom at one of its ends through which it is bonded to R 1 , R 1 is an aliphatic or heterocyclic or aromatic radical, the carbon chain of which may be interrupted by one or more B groups, R 5 is selected from the group consisting of (a) aliphatic radicals, wherein individual carbon atoms may be replaced by oxygen atoms or carbonyl groups, and wherein the carbon chains of same radicals may be optionally interrupted by a B group, and (b) araliphatic, cycloaliphatic, aromatic and heterocyclic radicals, wherein the carbon chain can be interrupted by one or more B structural elements and/or by one or more D coupling groups, R 3 , R 4 are hydrogen or aliphatic or araliphatic substituents, which are independent of one another, wherein the carbon chain can be interrupted by one or more B groups, B is selected from polymerizable or crosslinkable structural elements from the group comprising C 1 -C 16 -alkenyl, C 1 -C 16 -alkenyloxy, —C═C—, —CH═CH—COO—, —CH═CH—, —CX═CH—COO— with X═C 1 -C 16 -alkyl, and the trans-form of —OOC—CH═CH—COO—, and D is selected from —O—, —NH—, —N(CH 3 )—, —N(C 2 H 5 )—, —SO 2 —, —CO—, —COO—, —CH═CH—, —OCOO—, —OCH 2 —, CH═N, —CF 2 CF 2 —, as a chiral dopant in liquid crystal (mixtures), e.g., in electro-optical systems.
  • US9273247B2
    申请人:——
    公开号:US9273247B2
    公开(公告)日:2016-03-01
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