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12-(2-Thienyl)dodecanoic acid | 21010-10-6

中文名称
——
中文别名
——
英文名称
12-(2-Thienyl)dodecanoic acid
英文别名
12-thienyldodecanoic acid;12-thiophen-2-yl-dodecanoic acid;12-<2-Thienyl>-laurinsaeure;12-Thienyl-(2)-dodecansaeure;2-Thiophenelauric acid;12-thiophen-2-yldodecanoic acid
12-(2-Thienyl)dodecanoic acid化学式
CAS
21010-10-6
化学式
C16H26O2S
mdl
——
分子量
282.447
InChiKey
XQCGBAGJDHAMGX-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

  • 熔点:
    39.5-40.5 °C
  • 沸点:
    417.0±18.0 °C(Predicted)
  • 密度:
    1.040±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    5.9
  • 重原子数:
    19
  • 可旋转键数:
    12
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.69
  • 拓扑面积:
    65.5
  • 氢给体数:
    1
  • 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

  • Methods and Systems for Making Thiol Compounds from Terminal Olefinic Compounds
    申请人:Upshaw Thomas A.
    公开号:US20090264669A1
    公开(公告)日:2009-10-22
    The application discloses thiol ester molecules and α-hydroxy thiol ester molecules having a thiol group located on one of the final two carbon atoms in a carbon chain or a terminal or α-hydroxyl groups, respectively. The disclosed thiol ester molecules and or α-hydroxyl thiol ester molecules es may be made from unsaturated ester molecules having one or more terminal alkene groups. The disclosed techniques also provide methods for making unsaturated ester molecules having one or more terminal alkene groups by the metathesis of unsaturated esters having one or more internal carbon-carbon double bonds (e.g. natural source oils). The thiol ester molecules or α-hydroxy thiol ester molecule may be used in reactions with isocyanate monomers, epoxide monomer, or material having multiple alkene groups to make sealants, coatings, adhesives, and other products.
    本发明揭示了具有巴豆醇基位于碳链的最后两个碳原子之一或具有末端或α-羟基的巴豆醇酯分子和α-羟基巴豆醇酯分子。所述的巴豆醇酯分子或α-羟基巴豆醇酯分子可以由具有一个或多个末端烯烃基团的不饱和酯分子制备而成。本发明还提供了通过不饱和酯类之间的交换反应(例如天然源油)制备具有一个或多个末端烯烃基团的不饱和酯分子的方法。巴豆醇酯分子或α-羟基巴豆醇酯分子可以与异氰酸酯单体,环氧单体或具有多个烯烃基团的材料反应,制备密封剂,涂料,粘合剂和其他产品。
  • SYNTHESIS OF FUNCTIONALISED GOLD NANOPARTICLES AND NANOCOMPOUNDS CONTAINING SAME FOR MEASURING SUCROSE OR STARCH IN CELLS
    申请人:Pontificia Universidad Javeriana
    公开号:EP3567008A1
    公开(公告)日:2019-11-13
    The present invention relates to the field of industrial processes for measuring sugars and starch in cells and concerns the process of functionalising synthesized gold nanoparticles functionalized with polymer ligands, for the selective measurement of sucrose or starch in intracellular fluid. Also disclosed is a nanocompound for measuring the concentration of sucrose or starch in intracellular fluid, which contains synthesized gold nanoparticles functionalized with polymer ligands.
    本发明涉及测量细胞内糖和淀粉的工业工艺领域,涉及用聚合物配体功能化合成的纳米粒子的功能化过程,用于选择性测量细胞内液中的蔗糖或淀粉。此外,还公开了一种用于测量细胞内液中蔗糖或淀粉浓度的纳米化合物,其中含有用聚合物配体功能化的合成纳米颗粒。
  • Synthesis of functionalised gold nanoparticles and nanocompounds containing same for measuring sucrose or starch in cells
    申请人:PONTIFICIA UNIVERSIDAD JAVERIANA
    公开号:US11413683B2
    公开(公告)日:2022-08-16
    The present invention relates to the field of industrial processes for measuring sugars and starch in cells and concerns the process of functionalising synthesized gold nanoparticles functionalized with polymer ligands, for the selective measurement of sucrose or starch in intracellular fluid. Also disclosed is a nanocompound for measuring the concentration of sucrose or starch in intracellular fluid, which contains synthesized gold nanoparticles functionalized with polymer ligands.
    本发明涉及测量细胞内糖和淀粉的工业工艺领域,涉及用聚合物配体功能化合成的纳米粒子的功能化过程,用于选择性测量细胞内液中的蔗糖或淀粉。此外,还公开了一种用于测量细胞内液中蔗糖或淀粉浓度的纳米化合物,其中含有用聚合物配体功能化的合成纳米颗粒。
  • Ring-closure reactions. 16. An improved procedure for the synthesis of (2,5)thiophenophan-1-ones and its application to a convenient preparation of dl-muscone
    作者:Giuseppe Catoni、Carlo Galli、Luigi Mandolini
    DOI:10.1021/jo01298a029
    日期:1980.5
  • Ring-closure reactions. 14. Kinetics of macrocyclization by the intramolecular acylation of thiophene and benzothiophene compounds
    作者:C. Galli、G. Illuminati、L. Mandolini
    DOI:10.1021/jo01290a022
    日期:1980.1
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