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3-n-octylundecan-2-one | 89185-87-5

中文名称
——
中文别名
——
英文名称
3-n-octylundecan-2-one
英文别名
3-octyl-undecan-2-one;β-Oxo-γ-n-octylundecan;9-Aethanoyl-heptadecan;3-Octyl-undecan-2-on;asymm.Dioctyl-aceton;3-Octylundecan-2-one
3-n-octylundecan-2-one化学式
CAS
89185-87-5
化学式
C19H38O
mdl
——
分子量
282.51
InChiKey
VFRUZKGZGHGIHF-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:
    344.6±10.0 °C(Predicted)
  • 密度:
    0.831±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    8.2
  • 重原子数:
    20
  • 可旋转键数:
    15
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.95
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    1

SDS

SDS:dfb497db0380f65f00a81c29244852c3
查看

反应信息

  • 作为反应物:
    描述:
    3-n-octylundecan-2-one4-肼基苯甲酸硫酸 作用下, 以 乙醇 为溶剂, 反应 40.0h, 以31%的产率得到
    参考文献:
    名称:
    苯并[ c,d ]吲哚基不对称方酸染料在近红外染料敏化太阳能电池中的应用
    摘要:
    新颖苯并〔C,d ]基于假吲哚-不对称近红外方酸菁染料具有生发丁基(η  = 0.55%)和辛基(η  = 0.58%)基团在另一个假吲哚环显示出比通常使用的甲基衍生物更高的转换效率(η  = 0.38%)。的生发丁基和辛基可以抑制聚集的形成和接近我3 -种改善转换效率。
    DOI:
    10.1016/j.dyepig.2017.02.024
  • 作为产物:
    参考文献:
    名称:
    Guthzeit, Justus Liebigs Annalen der Chemie, 1880, vol. 204, p. 11
    摘要:
    DOI:
点击查看最新优质反应信息

文献信息

  • PRODRUGS OF NH-ACIDIC COMPOUNDS: ESTER, CARBONATE, CARBAMATE AND PHOSPHONATE DERIVATIVES
    申请人:Blumberg Laura Cook
    公开号:US20110319422A1
    公开(公告)日:2011-12-29
    The invention provides a method of sustained delivery of a lactam, imide, amide, sulfonamide, carbamate or urea containing parent drug by administering to a patient an effective amount of a prodrug compound of the invention wherein upon administration to the patient, release of the parent drug from the prodrug is sustained release. Prodrug compounds suitable for use in the methods of the invention are labile conjugates of parent drugs that are derivatized through carbonyl linked prodrug moieties. The prodrug compounds of the invention can be used to treat any condition for which the lactam, imide, amide, sulfonamide, carbamate or urea containing parent drug is useful as a treatment.
    该发明提供了一种持续释放内酰胺、亚酰胺、酰胺、磺胺碳酸酯或尿素含有母药的方法,通过向患者施用该发明的一种前药化合物的有效量,在向患者施用后,从前药中释放母药是持续释放的。适用于该发明方法的前药化合物是母药的不稳定结合物,通过羰基连接的前药基团进行衍生化。该发明的前药化合物可用于治疗任何需要内酰胺、亚酰胺、酰胺、磺胺碳酸酯或尿素含有母药作为治疗的情况。
  • [EN] POLYNUCLEOTIDES ENCODING LIPOPROTEIN LIPASE FOR THE TREATMENT OF HYPERLIPIDEMIA<br/>[FR] POLYNUCLÉOTIDES CODANT POUR LA LIPOPROTÉINE LIPASE DESTINÉS AU TRAITEMENT DE L'HYPERLIPIDÉMIE
    申请人:MODERNATX INC
    公开号:WO2017201333A1
    公开(公告)日:2017-11-23
    The invention relates to mRNA therapy for the treatment of hyperlipidemia. mRNAs for use in the invention, when administered in vivo, encode human lipoprotein lipase (LPL), isoforms thereof, functional fragments thereof, and fusion proteins comprising LPL. mRNAs of the invention are preferably encapsulated in lipid nanoparticles (LNPs) to effect efficient delivery to cells and/or tissues in subjects, when administered thereto, mRNA therapeaies of the invention increase and/or restore deficient levels of LPL expression and/or activity in subjects. mRNA therapies of the invention further decrease levels of triglycerides associated with deficient LPL activity in subjects.
    该发明涉及mRNA疗法用于治疗高脂血症。该发明中使用的mRNA,在体内给予时,编码人类脂蛋白脂肪酶LPL)、其异构体、其功能性片段以及包含LPL的融合蛋白。该发明中的mRNA最好被封装在脂质纳米颗粒(LNPs)中,以实现对受试者的细胞和/或组织的高效传递,当给予治疗时,该发明中的mRNA疗法增加和/或恢复受试者中LPL表达和/或活性的不足平。该发明中的mRNA疗法进一步降低与受试者中LPL活性不足相关的甘油三酯平。
  • Prodrugs of NH-Acidic Compounds: Ester, Carbonate, Carbamate and Phosphonate Derivatives
    申请人:Alkermes Pharma Ireland Limited
    公开号:US20150320875A1
    公开(公告)日:2015-11-12
    The invention provides a method of sustained delivery of a lactam, imide, amide, sulfonamide, carbamate or urea containing parent drug by administering to a patient an effective amount of a prodrug compound of the invention wherein upon administration to the patient, release of the parent drug from the prodrug is sustained release. Prodrug compounds suitable for use in the methods of the invention are labile conjugates of parent drugs that are derivatized through carbonyl linked prodrug moieties. The prodrug compounds of the invention can be used to treat any condition for which the lactam, imide, amide, sulfonamide, carbamate or urea containing parent drug is useful as a treatment.
    本发明提供了一种持续释放内酰胺、亚胺、酰胺、磺酰胺、氨基甲酸酯或尿素含量的母药的方法,通过向患者施用本发明的前药化合物的有效量,在患者体内释放母药的速率是持续释放的。适用于本发明方法的前药化合物是通过羰基偶联的前药基团衍生的母药的不稳定结合物。本发明的前药化合物可用于治疗任何需要内酰胺、亚胺、酰胺、磺酰胺、氨基甲酸酯或尿素含量的母药治疗的疾病。
  • Photoresist composition comprising cyclohexyleneoxyalkyl acrylates
    申请人:EASTMAN KODAK COMPANY (a New Jersey corporation)
    公开号:EP0300203A2
    公开(公告)日:1989-01-25
    A flexible and nonbrittle negative-working photoresist composition comprises a polymeric binder, a photoinitiator composition, and a polymerizable cyclohexyleneoxyalkyl acrylate monomer characterized by the structural formula: wherein R is H or CH₃, a is an integer of from 1 to 10 and b is 1 or 2.
    一种柔韧而不脆的底片工作光刻胶组合物包括聚合物粘合剂、光引发剂组合物和可聚合环己氧烷基丙烯酸酯单体,其结构式为:其中 R 为 H 或 CH₃,a 为 1 至 10 的整数,b 为 1 或 2。
  • Laminate for the formation of beam leads for IC chip bonding
    申请人:EASTMAN KODAK COMPANY (a New Jersey corporation)
    公开号:EP0300226A2
    公开(公告)日:1989-01-25
    A laminate, adapted for manufacturing frames of metal beam leads that are bonded to integrated circuit chips, comprises a) a flexible metal strip, b) a layer of a first resist adhered to one surface of the metal strip, and c) a layer of a second resist adhered to the opposite surface of the metal strip, the second resist being a negative-working resist comprising (1) a polymeric binder, (2) a photopolymerizable monomer mixture, and (3) a photoinitiator composition. The negative-working resist exhibits excellent flexibility and adhesion to the metal and superior performance during high temperature processing, whereby it serves effectively as a support for the beam leads.
    一种层压板,适用于制造与集成电路芯片粘接的属梁引线框架,包括 a) 柔性属带 b) 附着在属带一个表面上的第一抗蚀层,以及 c) 一层第二抗蚀层,粘附在属带的相反表面上、 第二光刻胶是一种负向工作光刻胶,包括 (1) 聚合物粘合剂 (2) 可光聚合的单体混合物,和 (3) 光引发剂组合物。 阴刻抗蚀层具有极佳的柔韧性和与属的附着力,在高温加工过程中性能优越,可有效地作为束引线的支撑。
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