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1,12-dodecanediylbis(methanesulfonate) | 106731-55-9

中文名称
——
中文别名
——
英文名称
1,12-dodecanediylbis(methanesulfonate)
英文别名
12-Methylsulfonyloxydodecyl methanesulfonate
1,12-dodecanediylbis(methanesulfonate)化学式
CAS
106731-55-9
化学式
C14H30O6S2
mdl
——
分子量
358.521
InChiKey
MZUWYNWIVQCHAE-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:
    515.6±23.0 °C(Predicted)
  • 密度:
    1.140±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.4
  • 重原子数:
    22
  • 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:
    104
  • 氢给体数:
    0
  • 氢受体数:
    6

反应信息

  • 作为反应物:
    描述:
    1,12-dodecanediylbis(methanesulfonate) 在 sodium iodide 作用下, 以 丙酮 为溶剂, 反应 16.0h, 以1.85 g的产率得到1,12-二碘十二烷
    参考文献:
    名称:
    Synthesis of both enantiomers of akolactone B and (+)-ancepsenolide
    摘要:
    The syntheses of (+)- and (-)-akolactone B and (+)-ancepsenolide were accomplished using a Pd-catalyzed carbonylation. As to the absolute configuration of akolactone B, making a comparison of the specific rotation of both enantiomers of synthetic akolactone B and the natural compound suggests that the absolute configuration at the 4-position of akolactone B is (R). (C) 2014 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetasy.2014.08.008
  • 作为产物:
    描述:
    1,12-十二烷二醇甲基磺酰氯三乙胺 作用下, 以 乙醚 为溶剂, 反应 1.0h, 生成 1,12-dodecanediylbis(methanesulfonate)
    参考文献:
    名称:
    Organocatalytic synthesis of new telechelic polycarbonates and study of their chemical reactivity
    摘要:
    A two-step versatile process for telechelic polycarbonates synthesis is described. 1-n-butyl-3-methylimidazolium-2-carboxylate (BMIM-2-CO2) was used as thermolabile precursor of N-heterocyclic carbene (NHC) organocatalyst. In a first step, synthesized branched fatty diols or commercially available linear diols were reacted with an excess of dimethylcarbonate (DMC) to afford oligocarbonates with methylcarbonate end-groups. Then, the methylcarbonate groups were reacted with hydroxyl groups of 9-decen-1-ol, 4-hexyn-1-ol and 4-hydroxybenzene ethanol leading to telechelic oligomers with alkene, alkyne and phenol functionalities. Reactivity of these end-groups towards polymerization was successfully evidenced. This procedure could be used for preparing a range of new telechelic oligocarbonates. (C) 2015 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.polymer.2015.04.046
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文献信息

  • [EN] BIVALENT BROMODOMAIN LIGANDS, AND METHODS OF USING SAME<br/>[FR] LIGANDS BROMODOMAINES BIVALENTS ET PROCÉDÉS D'UTILISATION DE CEUX-CI
    申请人:COFERON INC
    公开号:WO2015081284A1
    公开(公告)日:2015-06-04
    Described herein are compounds capable of modulating one or more biomolecules substantially simultaneously, e.g., modulating two or more binding domains (e.g., bromodomains) on a protein or on different proteins. For example, in one aspect, a bivalent compound or a pharmaceutically acceptable salt, stereoisomer, metabolite, or hydrate thereof is provided. In another aspect, a method of treating a disease associated with a protein having tandem bromodomains in a patient in need thereof is provided. The method comprises administering to the patient the bivalent compound as described.
    本文描述了一种能够同时调节一个或多个生物分子的化合物,例如,在蛋白质上或在不同蛋白质上调节两个或更多结合结构域(例如溴结构域)。例如,在一个方面,提供了一种二价化合物或药用盐、立体异构体、代谢物或其水合物。在另一个方面,提供了一种治疗与患有串联溴结构域蛋白相关的疾病的方法,该方法包括向患者注射所述的二价化合物。
  • Two-directional cascade molecules: synthesis and characterization of [9]-n-[9] arborols
    作者:George R. Newkome、Gregory R. Baker、Mary Jane Saunders、Paul S. Russo、Vinod K. Gupta、Zhong-qi Yao、Joseph E. Miller、Kelly Bouillion
    DOI:10.1039/c39860000752
    日期:——
    A series of two-directional cascade molecules (arborols) has been synthesized by a two-step nucleophilic substitution–amidation procedure; the [9]-10-[9] arborol forms a thermally reversible aqueous gel, which has been investigated via microscopy and light scattering techniques.
    通过两步亲核取代-酰胺化过程已经合成了一系列双向级联分子(硼烷)。[9] -10- [9]植烷醇形成热可逆的水凝胶,已通过显微镜和光散射技术对其进行了研究。
  • Processes using alpha, omega-difunctional aldaramides as monomers and crosslinkers
    申请人:Andrews Allen Mark
    公开号:US20060264672A1
    公开(公告)日:2006-11-23
    Processes using alpha, omega-difunctional aldaramides as monomers and crosslinkers are disclosed. The processes can be used to form polymers, particularly crosslinked polymers.
    本发明公开了使用α,ω-双官能团醛胺作为单体和交联剂的过程。该过程可用于形成聚合物,特别是交联聚合物。
  • PROCESSES FOR PREPARING POLYMERS USING ALPHA,OMEGA-DIFUNCTIONAL ALDARAMIDES
    申请人:Andrews Mark Allen
    公开号:US20080146768A1
    公开(公告)日:2008-06-19
    Processes using alpha, omega-difunctional aldaramides as monomers and crosslinkers are disclosed. The processes can be used to form polymers, particularly crosslinked polymers.
    本发明揭示了使用α,ω-二官能团醛胺作为单体和交联剂的过程。该过程可用于形成聚合物,特别是交联聚合物。
  • Cheng, P.; Blumstein, A.; Subramanyam, S., Molecular Crystals and Liquid Crystals Science and Technology, Section A: Molecular Crystals and Liquid Crystals, 1995, vol. 269, p. 1 - 38
    作者:Cheng, P.、Blumstein, A.、Subramanyam, S.
    DOI:——
    日期:——
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