2,3,5-三溴苯胺 | 609-17-6

• 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: 2,3,5-三溴苯胺
• 英文名称: 2,3,5-tribromo-aniline
• 英文别名: 2,3,5-Tribrom-anilin；2,3,5-Tribromoaniline
• CAS: 609-17-6
• 化学式: C₆H₄Br₃N
• 分子量: 329.816
• InChiKey: BRFIPEIKLLLCJW-UHFFFAOYSA-N

物化性质

• 沸点：
  333.5±37.0 °C(Predicted)
• 密度：
  2.351±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.3
• 重原子数：
  10
• 可旋转键数：
  0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  26
• 氢给体数：
  1
• 氢受体数：
  1

安全信息

• 海关编码：
  2921420090

反应信息

• 作为反应物：
  描述：

  2,3,5-三溴苯胺 在 盐酸 、 tetrafluoroboric acid 、 sodium nitrite 作用下， 生成 1-氟-2,3,5-三溴苯
  参考文献：
  名称：

  Pavlath; Olah, Acta Chimica Academiae Scientiarum Hungaricae, 1957, vol. 10, p. 227,229

  摘要：

  DOI：
• 作为产物：
  描述：

  2,3,5-tribromonitrobenzene 生成 2,3,5-三溴苯胺
  参考文献：
  名称：

  Claus; Wallbaum, Journal fur praktische Chemie (Leipzig 1954), 1897, vol. <2>56, p. 50

  摘要：

  DOI：

文献信息

• Polymer compound formed by condensing polyacrylic acid, polyamine and aromatic monoamine, intermediate composition, negative electrode, electrical storage device, slurry for negative electrode, method for producing polymer compound, and method for producing negative electrode
  申请人：KABUSHIKI KAISHA TOYOTA JIDOSHOKKI

  公开号：US10351672B2

  公开（公告）日：2019-07-16

  A polymer compound is formed by condensing a polyacrylic acid, a polyfunctional amine represented by the following general formula (1), and an aromatic monoamine. A chain structure constituted by the polyacrylic acid has free carboxyl groups and carboxyl groups to which the aromatic monoamines are bonded. Y is a straight-chain alkyl group having 1 to 4 carbon atoms, a phenylene group, or an oxygen atom. R1 and R2 are each independently one or more hydrogen atoms, a methyl group, an ethyl group, a trifluoromethyl group, or a methoxy group.

  一种聚合物化合物是由聚丙烯酸、以下通式（1）表示的多官能胺和芳香族单胺缩合而成。由聚丙烯酸构成的链结构具有自由羧基和芳香族单胺所键合的羧基。 Y 是具有 1 至 4 个碳原子的直链烷基、亚苯基或氧原子。R1 和 R2 各自独立地为一个或多个氢原子、甲基、乙基、三氟甲基或甲氧基。
• Phenyl benzenesulfonamides are novel and selective 5-HT6 antagonists: identification of N-(2,5-dibromo-3-fluorophenyl)-4-methoxy-3-piperazin-1-ylbenzenesulfonamide (SB-357134)
  作者：Steven M Bromidge、Stephen E Clarke、Tracey Gager、Kerry Griffith、Phillip Jeffrey、Andrew J Jennings、Graham F Joiner、Frank D King、Peter J Lovell、Stephen F Moss、Helen Newman、Graham Riley、Derek Rogers、Carol Routledge、Halina Serafinowska、Douglas R Smith

  DOI：10.1016/s0960-894x(00)00597-7

  日期：2001.1

  Substituted N-phenyl-4-methoxy-3-piperazin-1-ylbenzenesulfonamides and conformationally restricted analogues have been identified as high affinity and selective 5-HT6 antagonists. Compounds from this series had a range of pharmacokinetic profiles in rat and in general there was a correlation between clearance and CNS penetration. Based on its overall biological profile 2 (SB-357134) was selected for further pre-clinical evaluation. (C) 2000 Elsevier Science Ltd. All rights reserved.
• Nicolet; Ray, Journal of the American Chemical Society, 1927, vol. 49, p. 1805
  作者：Nicolet、Ray

  DOI：——

  日期：——
• Method for producing of polyarylene sulfides
  申请人：IDEMITSU PETROCHEMICAL CO. LTD.

  公开号：EP0215312B1

  公开（公告）日：1992-03-25
• COVALENT CONJUGATES OF COTTON AND SUBSTITUTES (VISCOSE, MODAL COTTON) WITH BIOACTIVE SUBSTANCES HAVING ANTISEPTIC, SANITIZING, ACARICIDAL AND INSECT REPELLENT ACTIVITY, AND A METHOD FOR OBTAINING THEM
  申请人：Franzoni Filati S.p.A.

  公开号：EP2035459A2

  公开（公告）日：2009-03-18