1-(2,5-二甲基苯基)乙胺 | 91251-26-2

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 中文名称: 1-(2,5-二甲基苯基)乙胺
• 中文别名: 1-(2,5-二甲基-苯基)-乙胺
• 英文名称: (+/-)-1-(2,5-dimethyl-phenyl)-ethylamine
• 英文别名: (+/-)-1-(2,5-Dimethyl-phenyl)-aethylamin；α,2,5-trimethylbenzylamine；α-(2,5-Dimethyl-phenyl)-aethylamin；1-(2,5-Dimethylphenyl)ethanamine
• CAS: 91251-26-2
• 化学式: C₁₀H₁₅N
• mdl: MFCD02177223
• 分子量: 149.236
• InChiKey: ULGHUDXDTMIEAM-UHFFFAOYSA-N

物化性质

• 沸点：
  223-225 °C
• 密度：
  0.9439 g/cm3(Temp: 17 °C)

计算性质

• 辛醇/水分配系数(LogP)：
  1.9
• 重原子数：
  11
• 可旋转键数：
  1
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.4
• 拓扑面积：
  26
• 氢给体数：
  1
• 氢受体数：
  1

安全信息

• 危险等级：
  IRRITANT
• 海关编码：
  2921499090
• WGK Germany：
  3

反应信息

• 作为反应物：
  描述：

  1-(2,5-二甲基苯基)乙胺 在 sulfuric acid mono-((R)-menthyl ester) 作用下， 生成 benzylidene-[(R)-1-(2,5-dimethyl-phenyl)-ethyl]-amine
  参考文献：
  名称：

  Potapow et al., Zhurnal Obshchei Khimii, 1959, vol. 29, p. 3139;engl.Ausg.S.3105

  摘要：

  DOI：
• 作为产物：
  描述：

  2,5-二甲基苯乙酮 在 ammonium formate 作用下， 生成 1-(2,5-二甲基苯基)乙胺
  参考文献：
  名称：

  Terentew; Potapow, Zhurnal Obshchei Khimii, 1957, vol. 27, p. 1092,1096;engl.Ausg.S.1176,1180

  摘要：

  DOI：

文献信息

• Non-fluorescent quencher compounds and biomolecular assays
  申请人：——

  公开号：US20030082547A1

  公开（公告）日：2003-05-01

  Bis-diazo,triaryl and aryldiazo-N-arylphenazonium quencher moieties, substituted with electron-withdrawing and electron-donating substituents which induce polarity in the delocalized aryl/diazo ring systems, are useful as labels when attached to biomolecules such as polynucleotides, nucleosides, nucleotides, and polypeptides. The quencher moieties are non-fluorescent and accept energy from fluorescent reporter labels by any energy-transfer mechanism, such as FRET. Fluorescence quencher compositions are useful in preparing quencher labelled biomolecules for various molecular biology assays based on fluorescence detection. 1

  双重重氮基、三芳基和芳基重氮-N-芳基苯酚盐猝灭基团，通过带电子吸引和电子给予取代基团引起芳基/重氮环系统极性，当连接到生物分子如多核苷酸、核苷、核苷酸和多肽时，可作为标签。这些猝灭基团是非荧光的，并通过任何能量转移机制（如FRET）从荧光报告标签吸收能量。荧光猝灭剂组合物在制备带有猝灭剂标记的生物分子，用于基于荧光检测的各种分子生物学分析中，非常有用。
• [EN] AZOLE-FUSED PYRIDAZIN-3(2H)-ONE DERIVATIVES<br/>[FR] DÉRIVÉS DE PYRIDAZIN-3(2H)-ONE FUSIONNÉS PAR UN AZOLE
  申请人：TAKEDA PHARMACEUTICALS CO

  公开号：WO2021055326A1

  公开（公告）日：2021-03-25

  Disclosed are compounds of Formula (1) and pharmaceutically acceptable salts thereof, wherein α, β, n, R4, R5, R6, R8, R9, R10, R11, X1, X2, X3 and X7 are defined in the specification. This disclosure also relates to materials and methods for preparing compounds of Formula (1), to pharmaceutical compositions comprising them, and to their use for treating diseases, disorders, and conditions associated with GPR139.

  揭示了Formula（1）的化合物及其药用可接受的盐，其中α、β、n、R4、R5、R6、R8、R9、R10、R11、X1、X2、X3和X7在规范中有定义。本公开还涉及制备Formula（1）化合物的材料和方法，包括含有它们的药物组合物，以及它们用于治疗与GPR139相关的疾病、紊乱和症状的用途。
• Process for producing optically active 3,3,3-trifluoro-2-hydroxy-2-methylpropionic acid, and salt thereof
  申请人：Sumitomo Chemical Company, Limited

  公开号：US20030232886A1

  公开（公告）日：2003-12-18

  There are disclosed imine compounds of formula (7) and (11), and processes for preparing the same: 1

  揭示了式（7）和式（11）的亚胺化合物，以及其制备过程：1
• NON-FLUORESCENT QUENCHER COMPOUNDS AND BIOMOLECULAR ASSAYS
  申请人：EWING Gregory J.

  公开号：US20090105452A1

  公开（公告）日：2009-04-23

  Bis-diazo, triaryl and aryldiazo-N-arylphenazonium quencher moieties, substituted with electron-withdrawing and electron-donating substituents which induce polarity in the delocalized aryl/diazo ring systems, are useful as labels when attached to biomolecules such as polynucleotides, nucleosides, nucleotides and polypeptides. The quencher moieties are non-fluorescent and accept energy transfer from fluorescent reporter labels by any energy-transfer mechanism, such as FRET. Fluorescence quencher compositions are useful in preparing quencher labeled biomolecules for various molecular biology assays based on fluorescence detection.

  双重重氮基团、三芳基和芳基重氮-N-芳基苯唑啉猝灭基团，通过在离域芳基/重氮环系统中引入电子受体和电子供体取代基，可以作为标签附加到生物分子上，如多核苷酸、核苷、核苷酸和多肽。这些猝灭基团是非荧光的，可以通过任何能量转移机制（例如FRET）从荧光报告标签接受能量转移。荧光猝灭剂组合物在制备标记生物分子的过程中非常有用，用于各种基于荧光检测的分子生物学测定。
• Non-Fluorescent Quencher Compounds and Biomolecular Assays
  申请人：Ewing Gregory J.

  公开号：US20110245462A1

  公开（公告）日：2011-10-06

  Bis-diazo, triaryl and aryldiazo-N-arylphenazonium quencher moieties, substituted with electron-withdrawing and electron-donating substituents which induce polarity in the delocalized aryl/diazo ring systems, are useful as labels when attached to biomolecules such as polynucleotides, nucleosides, nucleotides and polypeptides. The quencher moieties are non-fluorescent and accept energy transfer from fluorescent reporter labels by any energy-transfer mechanism, such as FRET. Fluorescence quencher compositions are useful in preparing quencher labeled biomolecules for various molecular biology assays based on fluorescence detection.

  双重重氮基团、三芳基和芳基重氮基-N-芳基苯并咪唑猝灭基团，通过引入电子吸引和电子给予取代基来诱导离域芳基/重氮环系统的极性，当附加到生物分子如多核苷酸、核苷、核苷酸和多肽时，它们可用作标签。猝灭基团是无荧光的，并且通过任何能量转移机制（如FRET），从荧光报告标签接受能量转移。荧光猝灭组合物在制备带有猝灭标记的生物分子用于基于荧光检测的各种分子生物学测定中非常有用。