N-(2-aminopropyl)-amino-4-nitroaniline-2-sulfonic acid

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: N-(2-aminopropyl)-amino-4-nitroaniline-2-sulfonic acid
• 英文别名: 2-[2-(2-Aminopropyl)hydrazinyl]-5-nitrobenzenesulfonic acid
• 化学式: C₉H₁₄N₄O₅S
• 分子量: 290.3
• InChiKey: ZREDTIMPVNVLOK-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -2
• 重原子数：
  19
• 可旋转键数：
  5
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  159
• 氢给体数：
  4
• 氢受体数：
  8

反应信息

• 作为产物：
  描述：

  2-氯-5-硝基苯磺酸 、 1,2-丙二胺 以 水 为溶剂， 生成 N-(2-aminopropyl)-amino-4-nitroaniline-2-sulfonic acid
  参考文献：
  名称：

  Reactive dyes from the dioxazine series, their preparation and use

  摘要：

  该公式的化合物描述如下：##STR1##，其中变量的定义如索赔中所述，适用作为纤维活性染料，可用于染色各种纤维材料。

  公开号：

  US05772698A1

文献信息

• Reaktivfarbstoffe der Dioxazinreihe, ihre Herstellung und Verwendung
  申请人：CIBA-GEIGY AG

  公开号：EP0739950A2

  公开（公告）日：1996-10-30

  Es werden Verbindungen der Formel worin die Variablen die in den Ansprüchen angegebene Bedeutung haben, beschrieben, welche als faserreaktive Farbstoffe zum Färben von verschiedensten Fasermaterialien geeignet sind.

  式中的化合物 其中的变量具有权利要求中给出的含义，适用于作为纤维活性染料对各种纤维材料进行染色。
• REACTIVE DYES, PROCESSES FOR THEIR PREPARATION AND THEIR USE
  申请人：Huntsman Advanced Materials (Switzerland) GmbH

  公开号：EP2201071A2

  公开（公告）日：2010-06-30
• US5772698A
  申请人：——

  公开号：US5772698A

  公开（公告）日：1998-06-30
• US7905928B2
  申请人：——

  公开号：US7905928B2

  公开（公告）日：2011-03-15
• [EN] REACTIVE DYES, PROCESSES FOR THEIR PREPARATION AND THEIR USE<br/>[FR] COLORANTS RÉACTIFS, LEURS PROCÉDÉS DE PRÉPARATION ET LEUR UTILISATION
  申请人：HUNTSMAN ADV MAT SWITZERLAND

  公开号：WO2009053238A2

  公开（公告）日：2009-04-30

  Reactive dyes of the formula (1) in which Q1 is hydrogen, halogen or a radical of the formula (2a) or (2b),R1, R2 and R3 independently of one another are hydrogen or C1-C4alkyl which is unsubstituted or substituted by hydroxyl, sulfo, carboxyl or sulfato, and R1 in formula (1) and R1 in formula (2a) have identical or different meanings and R2 in formula (1) and R2 in formula (2a) have identical or different meanings, (R4)0-1 and (R5)0-1 independently of one another are 0 or 1 identical or different substituents from the group consisting of C1-C4alkyl, C1-C4alkoxy, halogen and sulfo, A is hydrogen or C1-C4alkyl which is unsubstituted or substituted by hydroxyl, sulfo, carboxyl or sulfato, phenyl which is unsubstituted or substituted by C1-C4alkyl, C1-C4alkoxy, C2-C4alkanoylamino, hydroxyl, carboxyl, carbamoyl, sulfo or halogen, phenyl-C1-C2alkylene which is unsubstituted or substituted in the phenyl ring by C1-C4alkyl, C1-C4alkoxy, C2-C4alkanoylamino, hydroxyl, carboxyl, sulfo, carbamoyl or halogen, or C5-C7cycloalkyl which is unsubstituted or substituted by C1-C4alkyl, B is a C2-C12alkylene radical which can be interrupted by 1, 2 or 3 members from the group consisting of -NH-, -N(CH3)- or -O- and is unsubstituted or substituted by hydroxyl, sulfo, sulfato, cyano or carboxyl, a C5-C7cycloalkylene radical or C1-C2alkylene-C5-C7cycloalkylene radical which are unsubstituted or substituted in the cycloalkylring by C1C4alkyl,C1C2alkylenephenylene radical or phenylene radical which are unsubstituted or substituted in the phenyl ring by C1C4alkyl, C1C4alkoxy, C2-C4alkanoylamino, sulfo, halogen or carboxyl, V1 and V2 independently of one another are halogen, T is a radical of the formula -CO-(CH2)m-SO2-Y (3a), -CO-CH(HaI)-CH2-HaI (3b) or -CO-C(HaI)=CH2 (3c), Hal is halogen, X is hydroxyl or Y, Y is vinyl or a radical -CH2-CH2-U and U is a group which can be split off under alkaline conditions, and m is the number 2, 3 or 4. are suitable for dyeing widely varying fibre materials, in particular cellulosic fibre materials, and produce dyeings with good allround properties.