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2-decanoyl-6-methoxynaphthalene

中文名称
——
中文别名
——
英文名称
2-decanoyl-6-methoxynaphthalene
英文别名
2-Decanoyl-6-methoxynaphthalene;1-(6-methoxynaphthalen-2-yl)decan-1-one
2-decanoyl-6-methoxynaphthalene化学式
CAS
——
化学式
C21H28O2
mdl
——
分子量
312.452
InChiKey
AQIVSVNNVYRIEV-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):
    6.9
  • 重原子数:
    23
  • 可旋转键数:
    10
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.48
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

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文献信息

  • Novel Heterocyclic Compound, Method For Producing Intermediate Therefor, And Use Thereof
    申请人:Takimiya Kazuo
    公开号:US20130330876A1
    公开(公告)日:2013-12-12
    Provided are a novel heterocyclic compound represented by formula (1), and a field-effect transistor having a semiconductor layer comprising the aforementioned compound. Also provided is a method for producing an intermediate enabling the production of the aforementioned novel heterocyclic compound. (In the formula, R 1 and R 2 represent a hydrogen atom, a C 2-16 alkyl group or an aryl group. However, when R 1 each independently represents a C 2-16 alkyl group or an aryl group, R 2 represents a hydrogen atom or each independently represents an aryl group; and when R 1 represents a hydrogen atom, R 2 each independently represents an aryl group.)
    提供了一种由式(1)表示的新型杂环化合物,以及具有包含上述化合物的半导体层的场效应晶体管。还提供了一种生产中间体以便生产上述新型杂环化合物的方法。(在式中,R1和R2表示氢原子,C2-16烷基或芳基。但是,当R1各自独立表示C2-16烷基或芳基时,R2表示氢原子或各自独立表示芳基;当R1表示氢原子时,R2各自独立表示芳基。)
  • Heterocyclic dinaphtho thieno thiophene (DNTT) compounds for use as organic semiconductor thin films in field effect transistors and related methods
    申请人:Takimiya Kazuo
    公开号:US09018630B2
    公开(公告)日:2015-04-28
    Provided are a novel heterocyclic compound represented by formula (1), and a field-effect transistor having a semiconductor layer comprising the aforementioned compound. Also provided is a method for producing an intermediate enabling the production of the aforementioned novel heterocyclic compound. (In the formula, R1 and R2 represent a hydrogen atom, a C2-16 alkyl group or an aryl group. However, when R1 each independently represents a C2-16 alkyl group or an aryl group, R2 represents a hydrogen atom or each independently represents an aryl group; and when R1 represents a hydrogen atom, R2 each independently represents an aryl group.)
    提供了一种由式(1)表示的新型杂环化合物,以及具有包括上述化合物的半导体层的场效应晶体管。还提供了一种生产使上述新型杂环化合物的生产成为可能的中间体的方法。(在式中,R1和R2代表氢原子、C2-16烷基或芳基。但是,当R1各自独立地表示C2-16烷基或芳基时,R2表示氢原子或各自独立地表示芳基;当R1表示氢原子时,R2各自独立地表示芳基。)
  • US9018630B2
    申请人:——
    公开号:US9018630B2
    公开(公告)日:2015-04-28
  • NOVEL HETEROCYCLIC COMPOUND, METHOD FOR PRODUCING INTERMEDIATE THEREFOR, AND USE THEREOF
    申请人:Nippon Kayaku Kabushiki Kaisha
    公开号:EP2679592B1
    公开(公告)日:2018-10-03
  • Synthesis and Characterization of Liquid Crystalline Semiconducting Materials, Dialkyl-2-phenylnaphthalene Derivatives—Mesomorphic behavior and Charge carrier transport
    作者:Yukiko Takayashiki、Jun-Ich Hanna
    DOI:10.1080/15421400490435251
    日期:2004.1
    For establishment of high electronic charge carrier transport at ambient temperature, dialkyl derivatives of 2-phenylnaphthalene have been synthesized and characterized their liquid crystalline behaviors and photoelectrical properties. These materials exhibited smectic mesophases (Smectic A, B and E phases), at fairly low temperature range extended down below ambient temperature. Fast electronic transport of positive carriers was observed in SmE phase of 2-(4'-octylphenyl)-6-butylnaphthalene at 30degreesC, whose mobility was over 10(-2) cm(2)/Vs.
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