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5-(4-Hydroxyphenyl)-1-isopropylimidazole | 76134-12-8

中文名称
——
中文别名
——
英文名称
5-(4-Hydroxyphenyl)-1-isopropylimidazole
英文别名
4-(1-isopropyl-1H-imidazol-5-yl)phenol;4-(3-Propan-2-ylimidazol-4-yl)phenol
5-(4-Hydroxyphenyl)-1-isopropylimidazole化学式
CAS
76134-12-8
化学式
C12H14N2O
mdl
——
分子量
202.256
InChiKey
UDQGNUZUOPEHLW-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
  • 重原子数:
    15
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    38
  • 氢给体数:
    1
  • 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

  • DESIGN AND SYNTHESIS OF NOVEL INHIBITORS OF ISOPRENOID BIOSYNTHESIS
    申请人:BOARD OF TRUSTEES OF NORTHERN ILLINOIS UNIVERSITY
    公开号:US20150175582A1
    公开(公告)日:2015-06-25
    Antibacterial IspF inhibitor compounds and compositions are described. Methods include administering described compounds and compositions to treat bacterial or parasitic infections and to inhibit or parasite or bacterial growth.
    本文描述了抗菌IspF抑制剂化合物和组合物。方法包括给予所述化合物和组合物以治疗细菌或寄生虫感染并抑制寄生虫或细菌的生长。
  • DESIGN AND SYNTHESIS OF NOVEL INHIBITORS OF ISOPRENOID BIOSYNTHESIS (ISPF)
    申请人:BOARD OF TRUSTEES OF NORTHERN ILLINOIS UNIVERSITY
    公开号:US20160257655A1
    公开(公告)日:2016-09-08
    Antibacterial and antimalarial IspF inhibitor compounds and compositions are described. Methods include administering described compounds and compositions to treat bacterial or parasitic infections and to inhibit parasite or bacterial growth.
    本文描述了抗菌和抗疟疾的IspF抑制剂化合物和组合物。方法包括给予所述化合物和组合物以治疗细菌或寄生虫感染并抑制寄生虫或细菌的生长。
  • Heterocyclic derivatives of (4-aryloxymethyl-1.3-dioxolan-2-yl) methyl-1H-imidazoles and -1H-1.2.4-triazoles, their preparation and the derivatives for use as fungicides and bactericides
    申请人:JANSSEN PHARMACEUTICA N.V.
    公开号:EP0006712A1
    公开(公告)日:1980-01-09
    Compounds having the formula: and the pharmaceutically acceptable acid addition salts and stereochemically isomeric forms thereof, wherein: Q is a member selected from the group consisting of CH and N; Ar is a member selected from the group consisting of thienyl, halothienyl, phenyl and substituted phenyl; and Y is a member selected from the group consisting of optionally substituted pyrimidinyl, imidazolyl, oxazolyl, thiazolyl, pyrazolyl, isoxazolyl and oxadiazolyl. The compounds are useful as antifungal and antibacterial agents.
    具有以下式子的化合物 及其药学上可接受的酸加成盐和立体化学异构体,其中 Q 是选自 CH 和 N 组成的组的成员; Ar 是选自噻吩基、卤代噻吩基、苯基和取代苯基的成员;以及 Y 选自任选取代的嘧啶基、咪唑基、噁唑基、噻唑基、吡唑基、异噁唑基和噁二唑基组成的组。 这些化合物可用作抗真菌剂和抗菌剂。
  • Amaranzole A, a New <i>N</i>-Imidazolyl Steroid from <i>Phorbas amaranthus</i>
    作者:Brandon I. Morinaka、Makoto N. Masuno、Joseph R. Pawlik、Tadeusz F. Molinski
    DOI:10.1021/ol702325e
    日期:2007.12.1
    An unprecedented 24-N-imidazolyl steroidal alkaloid, amaranzole A, was isolated from a tropical sponge, Phorbas amaranthus. The structure was solved by interpretation of MS, NMR, including a novel exciton-coupled CD spectrum due to an allyl imidazole, and comparison with model compounds.
  • US4218458A
    申请人:——
    公开号:US4218458A
    公开(公告)日:1980-08-19
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