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

octyl 10-bromodecanoate | 1229225-67-5

中文名称
——
中文别名
——
英文名称
octyl 10-bromodecanoate
英文别名
Octyl 10-bromodecanoate
octyl 10-bromodecanoate化学式
CAS
1229225-67-5
化学式
C18H35BrO2
mdl
——
分子量
363.379
InChiKey
BPDGWRIUBDNPNE-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):
    6.41
  • 重原子数:
    21.0
  • 可旋转键数:
    16.0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.94
  • 拓扑面积:
    26.3
  • 氢给体数:
    0.0
  • 氢受体数:
    2.0

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    octyl 10-bromodecanoatepotassium phtalimideN,N-二甲基甲酰胺 为溶剂, 反应 4.0h, 生成
    参考文献:
    名称:
    Transkarbams as transdermal permeation enhancers: Effects of ester position and ammonium carbamate formation
    摘要:
    Transkarbam 12, an ammonium carbamate formed by the reaction of dodecyl 6-aminohexanoate with carbon dioxide, is a highly active, broad-spectrum, nontoxic, and nonirritant transdermal permeation enhancer. It probably acts by a dual mechanism: a part of its activity is associated with the carbamic acid salt and/or its decomposition in the acidic stratum corneum. The ammonium ester thereby released is an active enhancer species as well, and its activity highly depends on the position of the ester group. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2010.03.077
  • 作为产物:
    描述:
    辛醇10-溴癸酸氯仿 为溶剂, 反应 2.0h, 生成 octyl 10-bromodecanoate
    参考文献:
    名称:
    Transkarbams as transdermal permeation enhancers: Effects of ester position and ammonium carbamate formation
    摘要:
    Transkarbam 12, an ammonium carbamate formed by the reaction of dodecyl 6-aminohexanoate with carbon dioxide, is a highly active, broad-spectrum, nontoxic, and nonirritant transdermal permeation enhancer. It probably acts by a dual mechanism: a part of its activity is associated with the carbamic acid salt and/or its decomposition in the acidic stratum corneum. The ammonium ester thereby released is an active enhancer species as well, and its activity highly depends on the position of the ester group. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2010.03.077
点击查看最新优质反应信息

文献信息

  • [EN] IONIZABLE CATIONIC LIPIDS INCORPORATING SILICON<br/>[FR] LIPIDES CATIONIQUES IONISABLES COMPRENANT DU SILICIUM
    申请人:[en]ALDEXCHEM KFT.
    公开号:WO2024023174A2
    公开(公告)日:2024-02-01
    The invention relates to a novel ionizable cationic lipid family incorporating silicon, which belongs to the trademark LipexSil™ 1st generation lipids wherein at least one of the two side chains contains silyl acetal linker. Lipids containing silyl acetal linker(s) so far are unprecedented in the art and are effective as ionizable cationic lipids in the formulation of empty or loaded lipid nanoparticles (LNPs). The novel linkers according to the invention are designed by means of borane catalysts [WO 2022/129966]. The invention describes the synthesis of the lipids of formula (I), formation and characterization of nanoparticles and biological experiments demonstrating that the lipid nanoparticles prepared with these novel lipids can efficiently deliver their cargo (e.g. RNA, DNA, mRNA, siRNA, pDNA, circular DNA, small biologically active molecules) into the cells.
查看更多