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Decin-(5)-saeure-(1)-methylester | 18937-73-0

中文名称
——
中文别名
——
英文名称
Decin-(5)-saeure-(1)-methylester
英文别名
Methyl dec-5-ynoate
Decin-(5)-saeure-(1)-methylester化学式
CAS
18937-73-0
化学式
C11H18O2
mdl
——
分子量
182.263
InChiKey
HJMVKBXUUOQBJS-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):
    3
  • 重原子数:
    13
  • 可旋转键数:
    6
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.73
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

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

  • 作为产物:
    描述:
    甲醇5-癸炔酸咪唑三苯基膦 作用下, 以 二氯甲烷 为溶剂, 反应 0.08h, 以89%的产率得到Decin-(5)-saeure-(1)-methylester
    参考文献:
    名称:
    Mild Method for the Selective Esterification of Carboxylic Acids Based on the Garegg−Samuelsson Reaction
    摘要:
    A mild method for the selective esterification of primary alcohols is described. The use of different phosphines, I-2, and imidazole allows the selective esterification: of a wide variety of acids with excellent results. The generation of a bulky phosphonitun-carboxylate salt as intermediate could justify the selectivity observed in this process. Additionally, amides also can be synthesized with use of this method.
    DOI:
    10.1021/jo102395c
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文献信息

  • KETONE DERIVATIVES AND MEDICINAL USE THEREOF
    申请人:TORAY INDUSTRIES, INC.
    公开号:EP0841063A1
    公开(公告)日:1998-05-13
    The present invention relates to ketone derivatives represented by the following formula and medical agents cotaining the ketone derivatives or pharmacologically acceptable salts thereof as an active ingredient, and in particular, relates to a hematopoietic agent; it is shown that the present invention increases blood cells, such as platelets, white blood cells, and red blood cells, and is effective in preventing and treating cytopenia caused by cancer chemotherapy, radiation therapy, and the like.
    本发明涉及下式所代表的酮衍生物和以酮衍生物或其药理学上可接受的盐作为活性成分的医用制剂,特别是涉及一种造血制剂;本发明可增加血小板、白细胞和红细胞等血细胞,对预防和治疗癌症化疗、放疗等引起的细胞减少症有效。
  • Bohlmann,F. et al., Chemische Berichte, 1967, vol. 100, p. 3706 - 3715
    作者:Bohlmann,F. et al.
    DOI:——
    日期:——
  • US6215016B1
    申请人:——
    公开号:US6215016B1
    公开(公告)日:2001-04-10
  • Mild Method for the Selective Esterification of Carboxylic Acids Based on the Garegg−Samuelsson Reaction
    作者:Sara P. Morcillo、Luis Álvarez de Cienfuegos、Antonio J. Mota、José Justicia、Rafael Robles
    DOI:10.1021/jo102395c
    日期:2011.4.1
    A mild method for the selective esterification of primary alcohols is described. The use of different phosphines, I-2, and imidazole allows the selective esterification: of a wide variety of acids with excellent results. The generation of a bulky phosphonitun-carboxylate salt as intermediate could justify the selectivity observed in this process. Additionally, amides also can be synthesized with use of this method.
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