摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

5-(o-Tolyloxy)-pentylbromid | 23468-23-7

中文名称
——
中文别名
——
英文名称
5-(o-Tolyloxy)-pentylbromid
英文别名
Phenol, 2-methyl-O-[5-bromo-n-pentyl]-;1-(5-bromopentoxy)-2-methylbenzene
5-(o-Tolyloxy)-pentylbromid化学式
CAS
23468-23-7
化学式
C12H17BrO
mdl
——
分子量
257.17
InChiKey
VISZKYKRBYLOQA-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):
    4.5
  • 重原子数:
    14
  • 可旋转键数:
    6
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    9.2
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    5-(o-Tolyloxy)-pentylbromid2,4-二(三甲硅氧基)嘧啶 以 neat (no solvent) 为溶剂, 反应 1.0h, 生成 1-[5-(2-methylphenoxy)pentyl]uracil
    参考文献:
    名称:
    Synthesis and anti-HCMV activity of 1-[ω-(phenoxy)alkyl]uracil derivatives and analogues thereof
    摘要:
    HCMV infection represents a life-threatening condition for immunocompromised patients and newborn infants and novel anti-HCMV agents are clearly needed. In this regard, a series of 1-[omega-(phenoxy)alkyl]uracil derivatives were synthesized and examined for antiviral properties. Compounds 17, 20, 24 and 28 were found to exhibit highly specific and promising inhibitory activity against HCMV replication in HEL cell cultures with EC50 values within 5.5-12 mu M range. Further studies should be undertaken to elucidate the mechanism of action of these compounds and the structure-activity relationship for the linker region. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2013.05.009
  • 作为产物:
    描述:
    参考文献:
    名称:
    N-取代的S-2-氨基乙基硫代硫酸盐作为抗辐射剂。
    摘要:
    DOI:
    10.1021/jm00312a019
点击查看最新优质反应信息

文献信息

  • METHOD OF PRODUCING (METH)ACRYLOYL-TERMINATED POLYISOBUTYLENE POLYMER
    申请人:Kaneka Corporation
    公开号:EP3388454A1
    公开(公告)日:2018-10-17
    The object of the present invention is to provide a method for producing a (meth)acryloyl-terminated polyisobutylene polymer in which the auxiliary material used in the manufacture is easily removed, the burden of purification step and waste amount are decreased, and the transparency of the polymer is excellent. The method for producing the (meth)acryloyl-terminated polyisobutylene polymer contains a step 1 of polymerizing an isobutylene monomer under the presence of a Lewis acid catalyst to prepare a halogen-terminated polyisobutylene polymer (B), a step 2 of reacting the halogen-terminated polyisobutylene polymer (B) with a compound (C) having a halogen group and a phenoxy group under the presence a Lewis acid catalyst to prepare a halogenated phenoxyalkyl-terminated polyisobutylene polymer (D), and a step 3 of reacting the halogenated phenoxyalkyl-terminated polyisobutylene polymer (D) with an acrylic acid compound (E) to prepare the (meth)acryloyl-terminated polyisobutylene polymer (A).
    本发明的目的是提供一种生产(甲基)丙烯酰基封端的聚异丁烯聚合物的方法,该方法易于去除生产中使用的辅助材料,减少了纯化步骤的负担和废物量,并且聚合物的透明度极佳。(甲基)丙烯酰基封端聚异丁烯聚合物的生产方法包括步骤 1:在路易斯酸催化剂存在下聚合异丁烯单体,制备卤素封端聚异丁烯聚合物 (B)、步骤 2:在路易斯酸催化剂存在下,将卤素封端聚异丁烯聚合物(B)与具有卤素基和苯氧基的化合物(C)反应,制备卤代苯氧基烷基封端聚异丁烯聚合物(D),步骤 3:将卤代苯氧基烷基封端聚异丁烯聚合物(D)与丙烯酸化合物(E)反应,制备(甲基)丙烯酰基封端聚异丁烯聚合物(A)。
  • Method of producing (meth)acryloyl-terminated polyisobutylene polymer
    申请人:Kaneka Corporation
    公开号:US10604598B2
    公开(公告)日:2020-03-31
    A method for producing a (meth)acryloyl-terminated polyisobutylene polymer includes a step 1 of polymerizing an isobutylene monomer under the presence of a Lewis acid catalyst to prepare a halogen-terminated polyisobutylene polymer (B), a step 2 of reacting the halogen-terminated polyisobutylene polymer (B) with a compound (C) having a halogen group and a phenoxy group under the presence a Lewis acid catalyst to prepare a halogenated phenoxyalkyl-terminated polyisobutylene polymer (D), and a step 3 of reacting the halogenated phenoxyalkyl-terminated polyisobutylene polymer (D) with an acrylic acid compound (E) to prepare the (meth)acryloyl-terminated polyisobutylene polymer (A).
    一种生产(甲基)丙烯酰基封端聚异丁烯聚合物的方法包括以下步骤 1 在路易斯酸催化剂存在下聚合异丁烯单体,制备卤素封端聚异丁烯聚合物 (B)、步骤 2:在路易斯酸催化剂存在下,将卤素封端聚异丁烯聚合物(B)与具有卤素基团和苯氧基基团的化合物(C)反应,制备卤代苯氧基烷基封端聚异丁烯聚合物(D),步骤 3:将卤代苯氧基烷基封端聚异丁烯聚合物(D)与丙烯酸化合物(E)反应,制备(甲基)丙烯酰基封端聚异丁烯聚合物(A)。
  • SKIN CARE COMPOSITIONS COMPRISING PHENOXYALKYL AMINES
    申请人:Unilever PLC, a company registered in England and Wales under company no. 41424
    公开号:EP2498746B1
    公开(公告)日:2016-08-24
  • US8309064B2
    申请人:——
    公开号:US8309064B2
    公开(公告)日:2012-11-13
  • Synthesis and anti-HCMV activity of 1-[ω-(phenoxy)alkyl]uracil derivatives and analogues thereof
    作者:Mikhail S. Novikov、Denis A. Babkov、Maria P. Paramonova、Anastasia L. Khandazhinskaya、Alexander A. Ozerov、Alexander O. Chizhov、Graciela Andrei、Robert Snoeck、Jan Balzarini、Katherine L. Seley-Radtke
    DOI:10.1016/j.bmc.2013.05.009
    日期:2013.7
    HCMV infection represents a life-threatening condition for immunocompromised patients and newborn infants and novel anti-HCMV agents are clearly needed. In this regard, a series of 1-[omega-(phenoxy)alkyl]uracil derivatives were synthesized and examined for antiviral properties. Compounds 17, 20, 24 and 28 were found to exhibit highly specific and promising inhibitory activity against HCMV replication in HEL cell cultures with EC50 values within 5.5-12 mu M range. Further studies should be undertaken to elucidate the mechanism of action of these compounds and the structure-activity relationship for the linker region. (C) 2013 Elsevier Ltd. All rights reserved.
查看更多