diethyl-(2-fluoro-ethyl)-amine | 369-60-8

• 分子结构分类: 有机化合物 - 有机氮化合物
• 英文名称: diethyl-(2-fluoro-ethyl)-amine
• 英文别名: Diaethyl-(2-fluor-aethyl)-amin；2-Fluor-triaethylamin；2-Diethylaminoethylfluorid；Diethyl(2-fluoroethyl)amine；N,N-diethyl-2-fluoroethanamine
• CAS: 369-60-8
• 化学式: C₆H₁₄FN
• 分子量: 119.182
• InChiKey: MSPKPLPEMDTDDF-UHFFFAOYSA-N

物化性质

• 沸点：
  107-113 °C
• 密度：
  0.8775 g/cm3

计算性质

• 辛醇/水分配系数(LogP)：
  1.3
• 重原子数：
  8
• 可旋转键数：
  4
• 环数：
  0.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  3.2
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  2-二乙氨基乙硫醇 生成 diethyl-(2-fluoro-ethyl)-amine
  参考文献：
  名称：

  Fluorodesulfurization. A new reaction for the formation of carbon-fluorine bonds

  摘要：

  DOI：

  10.1021/jo00881a007

文献信息

• [EN] CELL-PERMEABLE PROBES FOR IDENTIFICATION AND IMAGING OF SIALIDASES<br/>[FR] SONDES PERMÉABLES AUX CELLULES POUR L'IDENTIFICATION ET L'IMAGERIE DE SIALIDASES
  申请人：ACADEMIA SINICA

  公开号：WO2014031498A1

  公开（公告）日：2014-02-27

  Provided herein are novel irreversible sialidase inhibitors. These compounds can be conjugated with a detectable tagging moiety such as azide-annexed biotin via CuAAC for isolation and identification of sialidases. The provided compounds and the corresponding detectable conjugates are useful for detecting sialidase-containing pathogens and imaging in situ sialidase activities under physiological conditions.

  提供了一种新型的不可逆唾液酸酶抑制剂。这些化合物可以通过点击化学（CuAAC）与可检测的标记基团（如叠氮基连在生物素上）进行偶联，用于分离和识别唾液酸酶。所提供的化合物及相应的可检测偶联物可用于检测含有唾液酸酶的病原体，以及在生理条件下对唾液酸酶活性进行成像。
• COMPOSITIONS AND METHODS FOR QUADRICYCLANE MODIFICATION OF BIOMOLECULES
  申请人：Sletten Ellen May

  公开号：US20130244267A1

  公开（公告）日：2013-09-19

  The present disclosure features a strain-promoted [2+2+2] reaction that can be carried out under physiological conditions. In general, the reaction involves reacting a pi-electrophile with a low lying LUMO with a quadricyclane on a biomolecule, generating a covalently modified biomolecule. The selectivity of the reaction and its compatibility with aqueous environments provides for its application in vivo and in vitro. The reaction is compatible with modification of living cells. In certain embodiments, the pi-electrophile can comprise a molecule of interest that is desired for delivery to a quadricyclane-containing biomolecule via [2+2+2] reaction.

  本公开揭示了一种在生理条件下可以进行的应变促进的[2+2+2]反应。一般来说，该反应涉及将一个π-亲电体与生物分子上的低能LUMO与四环烷基进行反应，生成一个共价修饰的生物分子。该反应的选择性及其与水性环境的兼容性使其可以在体内和体外应用。该反应与修饰活细胞兼容。在某些实施例中，π-亲电体可以包括所需用于通过[2+2+2]反应传递到含有四环烷基的生物分子的感兴趣分子。
• Compositions and Methods for Modification of Biomolecules
  申请人：JEWETT JOHN C.

  公开号：US20110207147A1

  公开（公告）日：2011-08-25

  Provided are modified cycloalkyne compounds; and methods of use of such compounds in modifying biomolecules. Embodiments include a cycloaddition reaction that can be carried out under physiological conditions. The cycloaddition reaction involves reacting a modified cycloalkyne with an azide moiety on a target biomolecule, generating a covalently modified biomolecule. The selectivity of the reaction and its compatibility with aqueous environments provide for its application in vivo and in vitro.

  提供了经修改的环炔烃化合物；以及使用这些化合物修改生物分子的方法。实施例包括可以在生理条件下进行的环加成反应。该环加成反应涉及将经修改的环炔烃与靶生物分子上的偶氮基团反应，生成共价修饰的生物分子。该反应的选择性及其与水性环境的兼容性使其适用于体内和体外应用。
• Compositions and methods for modification of biomolecules
  申请人：Bertozzi R. Carolyn

  公开号：US20060110782A1

  公开（公告）日：2006-05-25

  The present invention provides modified cycloalkyne compounds; and method of use of such compounds in modifying biomolecules. The present invention features a cycloaddition reaction that can be carried out under physiological conditions. In general, the invention involves reacting a modified cycloalkyne with an azide moiety on a target biomolecule, generating a covalently modified biomolecule. The selectivity of the reaction and its compatibility with aqueous environments provide for its application in vivo (e.g., on the cell surface or intracellularly) and in vitro (e.g., synthesis of peptides and other polymers, production of modified (e.g., labeled) amino acids).

  本发明提供了改性环烷炔化合物；以及使用这些化合物修饰生物分子的方法。本发明具有可以在生理条件下进行的环加成反应。一般来说，本发明涉及将改性环烷炔与目标生物分子上的偶氮基团反应，生成共价修饰的生物分子。该反应的选择性及其与水相环境的兼容性使其适用于体内应用（例如在细胞表面或细胞内）和体外应用（例如合成肽和其他聚合物，生产改性（例如标记）氨基酸）。
• COMPOSITIONS AND METHODS FOR MODIFICATION OF BIOMOLECULES
  申请人：BERTOZZI CAROLYN RUTH

  公开号：US20090068738A1

  公开（公告）日：2009-03-12

  The present invention provides modified cycloalkyne compounds; and method of use of such compounds in modifying biomolecules. The present invention features a cycloaddition reaction that can be carried out under physiological conditions. In general, the invention involves reacting a modified cycloalkyne with an azide moiety on a target biomolecule, generating a covalently modified biomolecule. The selectivity of the reaction and its compatibility with aqueous environments provide for its application in vivo (e.g., on the cell surface or intracellularly) and in vitro (e.g., synthesis of peptides and other polymers, production of modified (e.g., labeled) amino acids).

  本发明提供了改性的环烷炔化合物；以及使用这些化合物在修饰生物分子方面的方法。本发明特点是可以在生理条件下进行环加成反应。通常，本发明涉及将改性的环烷炔与目标生物分子上的偶氮基团反应，生成共价修饰的生物分子。该反应的选择性及其与水性环境的兼容性使其适用于体内（例如，细胞表面或细胞内）和体外（例如，合成肽和其他聚合物，生产改性（例如，标记）氨基酸）的应用。