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原甲酸三戊酯 | 637-42-3

中文名称
原甲酸三戊酯
中文别名
——
英文名称
Pentylorthoformiat
英文别名
Tripentyl orthoformate;1-(dipentoxymethoxy)pentane
原甲酸三戊酯化学式
CAS
637-42-3
化学式
C16H34O3
mdl
——
分子量
274.444
InChiKey
NRRGKWUTVHJHCS-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

物化性质

  • 沸点:
    101-103 °C(Press: 0.3 Torr)
  • 密度:
    0.8714 g/cm3

计算性质

  • 辛醇/水分配系数(LogP):
    5.4
  • 重原子数:
    19
  • 可旋转键数:
    15
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    27.7
  • 氢给体数:
    0
  • 氢受体数:
    3

安全信息

  • 海关编码:
    2909199090

SDS

SDS:0134407e03a1ad9279e1fb259dac26c5
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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

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文献信息

  • [EN] PHENYL-ANILINE SUBSTITUTED BICYCLIC COMPOUNDS USEFUL AS KINASE INHIBITORS<br/>[FR] COMPOSES BICYCLIQUES A SUBSTITUTION PHENYL-ANILINE UTILISES COMME INHIBITEUR DE LA KINASE
    申请人:BRISTOL MYERS SQUIBB CO
    公开号:WO2005042537A1
    公开(公告)日:2005-05-12
    Compounds having the formula (I), and pharmaceutically acceptable salts, prodrugs, and solvates thereof, are useful as kinase inhibitors, wherein R, R1 , R2, R5, R6a, R6b, J, K, X and Z are as described in the specification.
    具有化学式(I)的化合物,以及其药学上可接受的盐、前药和溶剂化合物,可用作激酶抑制剂,其中R、R1、R2、R5、R6a、R6b、J、K、X和Z如规范中所述。
  • Process for preparing 4,5-dihydro-pyrazolo[3,4-c]pyrid-2-ones
    申请人:Shapiro Rafael
    公开号:US20060069258A1
    公开(公告)日:2006-03-30
    A novel process and intermediates thereof for making 4,5-dihydro-pyrazolo[3,4-c]pyrid-2-ones of the type shown below from appropriate phenyl hydrazines is described. These compounds can be useful as factor Xa inhibitors.
    一种从适当的苯基制备下述类型的4,5-二氢吡唑并中间体的新工艺被描述。这些化合物可用作因子Xa抑制剂
  • Asymmetric Synthesis of Cyclic Hydroxy Ketones Derived from Enol Ethers via Sharpless Asymmetric Dihydroxylation. A Study in the Correlation of the Enol Ether Chain Length and Enantioselectivity
    作者:Benjamin F. Marcune、Sandor Karady、Paul J. Reider、Ross A. Miller、Mirlinda Biba、Lisa DiMichele、Robert A. Reamer
    DOI:10.1021/jo034854o
    日期:2003.10.1
    The Sharpless asymmetric dihydroxylation reaction of enol ethers derived from their corresponding cyclic ketones, gave alpha-hydroxyketones with high enantioselectivity. The enantiomeric excess was found to be proportional to the length of the unbranched enol ether chain with a maximum ee for the pentyl enol ether. An efficient synthesis of alpha-hydroxy chromanone in >90% ee was demonstrated using
    衍生自其相应的环酮的烯醇醚的Sharpless不对称二羟基化反应,得到具有高对映选择性的α-羟基酮。发现对映体过量与直链烯醇醚链的长度成正比,对于戊烯基烯醇醚具有最大ee。使用该方法证明了在> 90%ee中有效合成α-羟基苯并二氢吡喃酮
  • [EN] FUNCTIONALIZED α-ANGELICA LACTONE MONOMERS AND POLYMERS OBTAINED THEREFROM<br/>[FR] MONOMÈRES α-ANGELICA LACTONE ET POLYMÈRES OBTENUS À PARTIR DE CEUX-CI
    申请人:HENKEL AG & CO KGAA
    公开号:WO2020212041A1
    公开(公告)日:2020-10-22
    The present invention is directed to a monomer for chain growth polymerization, in particular anionic polymerization, said monomer having the general formula (EFL) wherein: Ra is a C3-C30 alkyl, C3-C30 cycloalkyl, C6-C18 aryl or C2-C12 alkenyl group. The present invention is further directed to a process for the anionic polymerization of at least one compound (EFL) as defined above, wherein said anionic polymerization is conducted in the presence of an initiator selected from the group consisting of: alkali metal organyls; alkali metal alkoxides; alkali metal thiolate; alkali metal amides; and, compounds of an element of group 3a of the Periodic Table of the Elements. The process of anionic polymerization yields a homo- or co-polymer (p-EFL) having pendant lactone functional groups in its repeating units.
    本发明涉及一种用于链增长聚合的单体,特别是阴离子聚合,所述单体具有通式(EFL),其中:Ra是C3-C30烷基,C3-C30环烷基,C6-C18芳基或C2-C12烯基基团。本发明进一步涉及一种用于上述定义的至少一种化合物(EFL)的阴离子聚合的方法,其中所述阴离子聚合在以下引发剂的存在下进行:碱属有机基;碱属烷氧基;碱醇酸盐;碱属酰胺;以及元素3a族化合物。阴离子聚合的方法产生具有其重复单元中端基内酯官能团的同聚物或共聚物(p-EFL)。
  • [EN] PROCESSES FOR THE PREPARATION OF IVACAFTOR<br/>[FR] PROCÉDÉS DE PRÉPARATION D'IVACAFTOR
    申请人:LAURUS LABS PRIVATE LTD
    公开号:WO2017037672A1
    公开(公告)日:2017-03-09
    The present invention provides processes for the preparation of ivacaftor using novel intermediates and a process for its preparation.
    本发明提供了使用新型中间体制备依维卡夫醇的工艺以及其制备工艺。
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