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malonic acid N-hydroxylsuccinimidyl half ester

中文名称
——
中文别名
——
英文名称
malonic acid N-hydroxylsuccinimidyl half ester
英文别名
N-hydroxysuccinimidyl malonate;3-((2,5-Dioxopyrrolidin-1-yl)oxy)-3-oxopropanoic acid;3-(2,5-dioxopyrrolidin-1-yl)oxy-3-oxopropanoic acid
malonic acid N-hydroxylsuccinimidyl half ester化学式
CAS
——
化学式
C7H7NO6
mdl
——
分子量
201.136
InChiKey
SKCBDTKJZDYLQS-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):
    -1.1
  • 重原子数:
    14
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.43
  • 拓扑面积:
    101
  • 氢给体数:
    1
  • 氢受体数:
    6

反应信息

  • 作为反应物:
    描述:
    辅酶 Amalonic acid N-hydroxylsuccinimidyl half ester碳酸氢钠 作用下, 以 丙酮 为溶剂, 反应 12.17h, 以93.8%的产率得到丙二酰辅酶A-钠盐
    参考文献:
    名称:
    Rapid preparation of (methyl)malonyl coenzyme A and enzymatic formation of unusual polyketides by type III polyketide synthase from Aquilaria sinensis
    摘要:
    (Methyl) malonyl coenzyme A was rapidly and effectively synthesized by a two-step procedure involving preparation of N-hydroxysuccinimidyl (methyl) malonate from (methyl) Meldrum's acid, and followed by transesterification with coenzyme A. The synthesized (methyl) malonyl coenzyme A could be well accepted and assembled to 4-hydroxy phenylpropionyl coenzyme A by type III polyketide synthase from Aquilaria sinensis to produce dihydrochalcone and 4-hydroxy-3,5-dimethyl-6-(4-hydroxyphenethyl)-2H-pyrone as well as 4-hydroxy-3,5-dimethyl-6-(5-(4-hydroxyphenyl)-3-oxopentan-2-yl)-2H-pyrone. (C) 2015 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2015.01.045
  • 作为产物:
    描述:
    N-羟基丁二酰亚胺丙二酸环(亚)异丙酯甲苯 为溶剂, 以54%的产率得到malonic acid N-hydroxylsuccinimidyl half ester
    参考文献:
    名称:
    活化丙二酸半酯的自缩合:聚酮化合物生物合成中脱羧性克莱森缩合的模型
    摘要:
    丙二酸半含氧酸酯与N-羟基琥珀酰亚胺基酯形成试剂的反应导致自缩合,从而提供相应的1,3-丙酮二羧酸二酯。此新方法不需要二价金属螯合剂或配位溶剂即可成功缩合。
    DOI:
    10.1016/j.tetlet.2003.08.014
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文献信息

  • Self-condensation of activated malonic acid half esters: a model for the decarboxylative Claisen condensation in polyketide biosynthesis
    作者:Youngha Ryu、A.Ian Scott
    DOI:10.1016/j.tetlet.2003.08.014
    日期:2003.9
    The reaction of a malonic acid half oxyester with a N-hydroxysuccinimidyl ester-forming reagent resulted in self-condensation to provide the corresponding 1,3-acetonedicarboxylic acid diester. This new method does not require a divalent metal chelator or a coordinating solvent for successful condensation.
    丙二酸半含氧酸酯与N-羟基琥珀酰亚胺基酯形成试剂的反应导致自缩合,从而提供相应的1,3-丙酮二羧酸二酯。此新方法不需要二价金属螯合剂或配位溶剂即可成功缩合。
  • SILOXANE LIGANDS TO BE USED FOR DISPERSING QUANTUM DOTS IN SILICONE HOSTS TO OBTAIN COLOR CONVERTERS FOR LED LIGHTING
    申请人:KONINKLIJKE PHILIPS N.V.
    公开号:US20170222097A1
    公开(公告)日:2017-08-03
    The invention provides a luminescent material comprising wavelength converter nanoparticles ( 120 ) with siloxane polymer capping ligands ( 130 ) associated to the wavelength converter nanoparticles ( 120 ), wherein the siloxane polymer capping ligands ( 130 ) comprise siloxane polymers which comprise at least one capping group comprising a terminal carboxylic acid group, wherein the capping group comprises in total at least six carbon atoms.
  • Rapid preparation of (methyl)malonyl coenzyme A and enzymatic formation of unusual polyketides by type III polyketide synthase from Aquilaria sinensis
    作者:Bo-Wen Gao、Xiao-Hui Wang、Xiao Liu、She-Po Shi、Peng-Fei Tu
    DOI:10.1016/j.bmcl.2015.01.045
    日期:2015.3
    (Methyl) malonyl coenzyme A was rapidly and effectively synthesized by a two-step procedure involving preparation of N-hydroxysuccinimidyl (methyl) malonate from (methyl) Meldrum's acid, and followed by transesterification with coenzyme A. The synthesized (methyl) malonyl coenzyme A could be well accepted and assembled to 4-hydroxy phenylpropionyl coenzyme A by type III polyketide synthase from Aquilaria sinensis to produce dihydrochalcone and 4-hydroxy-3,5-dimethyl-6-(4-hydroxyphenethyl)-2H-pyrone as well as 4-hydroxy-3,5-dimethyl-6-(5-(4-hydroxyphenyl)-3-oxopentan-2-yl)-2H-pyrone. (C) 2015 Elsevier Ltd. All rights reserved.
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