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prop-2-enyl 3-[5-[(Z)-(4-ethyl-3-methyl-5-oxopyrrol-2-ylidene)methyl]-4-methyl-1H-pyrrol-3-yl]propanoate | 215871-86-6

中文名称
——
中文别名
——
英文名称
prop-2-enyl 3-[5-[(Z)-(4-ethyl-3-methyl-5-oxopyrrol-2-ylidene)methyl]-4-methyl-1H-pyrrol-3-yl]propanoate
英文别名
——
prop-2-enyl 3-[5-[(Z)-(4-ethyl-3-methyl-5-oxopyrrol-2-ylidene)methyl]-4-methyl-1H-pyrrol-3-yl]propanoate化学式
CAS
215871-86-6
化学式
C19H24N2O3
mdl
——
分子量
328.411
InChiKey
XTJFUNRANVABMT-YVLHZVERSA-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):
    2.4
  • 重原子数:
    24
  • 可旋转键数:
    8
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.37
  • 拓扑面积:
    71.2
  • 氢给体数:
    2
  • 氢受体数:
    3

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
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • Efficient Construction of A,B-Rings Component for Syntheses of Phycocyanobilin and Its Derivative
    作者:Krishanthi Padmarani Jayasundera、Hideki Kinoshita、Katsuhiko Inomata
    DOI:10.1246/cl.1998.1227
    日期:1998.12
    Total syntheses of phycocyanobilin and its photoactivatable derivative were accomplished by developing a new and versatile method for the construction of A,B-rings component, which consists of the Wittig-type new coupling reaction of 4-(1-methoxyethyl)-3-methyl-5-tosyl-1,5-dihydro-2H-pyrrol-2-one and a 2-formyl pyrrole derivative in the presence of nBu3P and a base, followed by reduction with aluminum amalgam and subsequent acid treatment.
    该方法包括 4-(1-甲氧基乙基)-3-甲基-5-对甲苯磺酰基-1,5-二氢-2H-吡咯-2-酮和 2-甲酰基吡咯衍生物在 nBu3P 和碱存在下的 Wittig 型新偶联反应,然后用铝汞齐还原并进行酸处理。
  • An Efficient Method for the Conversion of 2-Bromo-5-tosylpyrroles to the Corresponding 5-Tosylpyrrolinones as the D-Ring of Phycocyanobilin Derivatives
    作者:Shuzo Takeda、Krishanthi Padmarani Jayasundera、Takashi Kakiuchi、Hideki Kinoshita、Katsuhiko Inomata
    DOI:10.1246/cl.2001.590
    日期:2001.6
    2-Bromo-5-tosylpyrroles were efficiently converted to the corresponding 5-tosylpyrrolinones as the D-ring of phycocyanobilin (PCB) derivatives by treating with DMSO and Zn in TFA in the presence of a catalytic amount of iodine. PCB derivatives modified at the D-ring were prepared in free acid forms employing the resulting 5-tosylpyrrolinones toward structure/function analysis of phytochrome.
    在一定量的碘催化下,在反式脂肪酸中用二甲基亚砜和锌处理 2-溴-5-对甲苯磺酰基吡咯烷,可有效地将其转化为相应的 5-对甲苯磺酰基吡咯烷酮,作为植物花青素(PCB)衍生物的 D 环。利用得到的 5-对甲苯磺酰基吡咯烷酮对植物色素进行结构/功能分析。
  • Total Syntheses of Phycocyanobilin Derivatives Bearing a Modified A-Ring toward the Structure/Function Analysis of Phytochrome
    作者:Daisuke Sawamoto、Hiroshi Nakamura、Hideki Kinoshita、Shuhei Fujinami、Katsuhiko Inomata
    DOI:10.1246/cl.2000.1398
    日期:2000.12
    Phycocyanobilin (PCB) derivatives bearing a modified A-ring, including 3,3′-dihydrogenated PCB derivatives, were efficiently synthesized in free acid forms by applying our original methods for the preparation of A-, A/B-, and C/D-ring components toward the structure/function analysis of phytochrome.
    为了对植物色素进行结构/功能分析,我们采用独创的 A-环、A/B-环和 C/D 环成分制备方法,高效合成了具有修饰 A 环的植物花青素(PCB)衍生物,包括 3,3′-二氢化 PCB 衍生物的游离酸形式。
  • A Highly Efficient Method for the Preparation of the A/B-Ring Component of Phycobilin Derivatives Starting from Bilirubin
    作者:Daisuke Sawamoto、Katsuhiko Inomata
    DOI:10.1246/cl.2001.588
    日期:2001.6
    An efficient synthetic method of the A/B-ring component of phycobilin derivatives (PΦB and PCB) was established by using bilirubin as a starting material, which allows to construct the phycobilins in a few steps.
    以胆红素为起始原料,建立了一种高效的合成方法,只需几个步骤就能合成植物纤毛素衍生物(PΦB 和 PCB)的 A/B 环成分。
  • An Efficient Method to Construct the A,B-Rings Component toward Total Syntheses of Phycocyanobilin and Its Derivative as a Photoprobe
    作者:Krishanthi Padmarani Jayasundera、Hideki Kinoshita、Katsuhiko Inomata
    DOI:10.1246/bcsj.73.497
    日期:2000.2
    Total syntheses of phycocyanobilin and its derivative bearing a photoreactive group at the D-ring were accomplished by developing a new and efficient method for the construction of A,B-rings component, which consists of the Wittig-type new coupling reaction of 4-(1-methoxyethyl or 1-tosylethyl)-3-methyl-5-tosyl-1,5-dihydro-2H-pyrrol-2-one and a 2-formyl pyrrole derivative in the presence of nBu3P and a base, followed by reduction with aluminum amalgam and a subsequent acid or base treatment.
    通过开发一种新颖且高效的方法构建A、B环部分,成功完成了藻蓝蛋白胆色素及其在D环上具有光反应基团的衍生物的总合成。该方法包括在nBu3P和碱存在下,4-(1-甲氧基乙基或1-托烯乙基)-3-甲基-5-托烯-1,5-二氢-2H-吡咯烷-2-酮与2-呋喃基吡咯衍生物的Wittig型新偶联反应,随后用铝齐聚物还原,并进行酸或碱处理。
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