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2-(4-tert-butylphenyl)-6-methoxybenzo[b]furan | 1429209-48-2

中文名称
——
中文别名
——
英文名称
2-(4-tert-butylphenyl)-6-methoxybenzo[b]furan
英文别名
2-(4-tert-butylphenyl)-6-methoxybenzofuran;2-(4-Tert-butylphenyl)-6-methoxy-1-benzofuran;2-(4-tert-butylphenyl)-6-methoxy-1-benzofuran
2-(4-tert-butylphenyl)-6-methoxybenzo[b]furan化学式
CAS
1429209-48-2
化学式
C19H20O2
mdl
——
分子量
280.367
InChiKey
REUOBTZNRXJAQE-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):
    5.6
  • 重原子数:
    21
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.26
  • 拓扑面积:
    22.4
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

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文献信息

  • Palladium-Catalyzed Addition of Potassium Aryltrifluoroborates to Aliphatic Nitriles: Synthesis of Alkyl Aryl Ketones, Diketone Compounds, and 2-Arylbenzo[<i>b</i>]furans
    作者:Xingyong Wang、Miaochang Liu、Long Xu、Qingzong Wang、Jiuxi Chen、Jinchang Ding、Huayue Wu
    DOI:10.1021/jo400433m
    日期:2013.6.7
    developed, leading to a wide range of alkyl aryl ketones with moderate to excellent yields. Moreover, several dinitriles (e.g., malononitrile, glutaronitrile, and adiponitrile) were applicable to this process for the construction of 1,3-, 1,5-, or 1,6-dicarbonyl compounds. The scope of the developed approach is successfully explored toward the one-step synthesis of 2-arylbenzo[b]furans via sequential
    已经开发了钯催化的芳基三氟硼酸钾加成到脂肪族腈中的方法,从而产生了范围广泛的烷基芳基酮,并具有中等至极好的收率。此外,几种二腈(例如丙二腈,戊二腈和己二腈)适用于该方法,用于构建1,3-,1,5-或1,6-二羰基化合物。通过顺序加成和分子内环化反应,一步一步合成2-芳基苯并[ b ]呋喃已成功探索了所开发方法的范围。该方法学接受了广泛的底物,并适用于文库合成。
  • DIARYLETHENE COMPOUNDS AND USES THEREOF
    申请人:SWITCH MATERIALS, INC.
    公开号:US20160083398A1
    公开(公告)日:2016-03-24
    A compound according to Formula IA and IB, reversibly convertible under photochromic and electrochromic conditions between a ring-open isomer A and a ring-closed isomer B is provided. For substitutent groups, Z is N, O or S; each R 1 is independently selected from the group consisting of H, or halo; each R 2 is independently selected from the group consisting of H, halo, a polymer backbone, alkyl or aryl; or, when both R 2 together form —CH═CH— and form part of a polymer backbone; each R 3 is independently selected from the group consisting of H, halo, alkyl, alkoxy, thioalkyl or aryl; each R 4 is aryl; and each R 5 is independently selected from the group consisting of H, halo, alkyl, alkoxy, thioalkyl or aryl.
    本发明提供了一种按照式IA和IB的化合物,在光致变色和电致变色条件下,可在环开放异构体A和环闭合异构体B之间可逆地转化。对于取代基,Z为N、O或S;每个R1独立地选自H或卤素;每个R2独立地选自H、卤素、聚合物骨架、烷基或芳基;或者,当两个R2一起形成-CH═CH-并形成聚合物骨架的一部分时;每个R3独立地选自H、卤素、烷基、烷氧基、硫代烷基或芳基;每个R4为芳基;每个R5独立地选自H、卤素、烷基、烷氧基、硫代烷基或芳基。
  • Diarylethene compounds and uses thereof
    申请人:SWITCH MATERIALS, INC.
    公开号:US10072023B2
    公开(公告)日:2018-09-11
    A compound according to Formula IA and IB, reversibly convertible under photochromic and electrochromic conditions between a ring-open isomer A and a ring-closed isomer B is provided. For substitutent groups, Z is N, O or S; each R1 is independently selected from the group consisting of H, or halo; each R2 is independently selected from the group consisting of H, halo, a polymer backbone, alkyl or aryl; or, when both R2 together form —CH═CH— and form part of a polymer backbone; each R3 is independently selected from the group consisting of H, halo, alkyl, alkoxy, thioalkyl or aryl; each R4 is aryl; and each R5 is independently selected from the group consisting of H, halo, alkyl, alkoxy, thioalkyl or aryl.
    提供了一种根据式 IA 和 IB 的化合物,该化合物在光致变色和电致变色条件下可在开环异构体 A 和闭环异构体 B 之间进行可逆转换。对于取代基,Z 是 N、O 或 S;每个 R1 独立地选自 H 或卤代;每个 R2 独立地选自 H、卤代、聚合物骨架、烷基或芳基;或者,当两个 R2 一起形成 -CH═CH- 并构成聚合物骨架的一部分时;每个 R3 独立地选自由 H、卤素、烷基、烷氧基、硫代烷基或芳基组成的组;每个 R4 是芳基;每个 R5 独立地选自由 H、卤素、烷基、烷氧基、硫代烷基或芳基组成的组。
  • US20140256936A1
    申请人:——
    公开号:US20140256936A1
    公开(公告)日:2014-09-11
  • PHOTOCHROMIC AND ELECTROCHROMIC DIARYLCYCLOPENTENE DERIVATIVES AS OPTICAL FILTERS
    申请人:SWITCH MATERIALS, INC.
    公开号:US20180339995A1
    公开(公告)日:2018-11-29
    A compound according to Formula IA and IB, reversibly convertible under photochromic and electrochromic conditions between a ring-open isomer A and a ring-closed isomer B is provided. For substitutent groups, Z is N, O or S; each R 1 is independently selected from the group consisting of H, or halo; each R 2 is independently selected from the group consisting of H, halo, a polymer backbone, alkyl or aryl; or, when both R 2 together form —CH═CH— and form part of a polymer backbone; each R 3 is independently selected from the group consisting of H, halo, alkyl, alkoxy, thioalkyl or aryl; each R 4 is aryl; and each R 5 is independently selected from the group consisting of H, halo, alkyl, alkoxy, thioalkyl or aryl.
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