3,10-diamino-6,13-dichloro-[1,4]benzoxazino[2,3-b]phenoxazine-4,11-disulfonic acid

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并恶嗪类
• 英文名称: 3,10-diamino-6,13-dichloro-[1,4]benzoxazino[2,3-b]phenoxazine-4,11-disulfonic acid
• 化学式: C₁₈H₁₀Cl₂N₄O₈S₂
• 分子量: 545.3
• InChiKey: FEHDDMUMJIFOOE-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2
• 重原子数：
  34
• 可旋转键数：
  2
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  221
• 氢给体数：
  4
• 氢受体数：
  12

反应信息

• 作为反应物：
  描述：

  3,10-diamino-6,13-dichloro-[1,4]benzoxazino[2,3-b]phenoxazine-4,11-disulfonic acid 生成 10-amino-3-[(10-amino-6,13-dichloro-4,11-disulfo-[1,4]benzoxazino[2,3-b]phenoxazin-3-yl)carbamoylamino]-6,13-dichloro-[1,4]benzoxazino[2,3-b]phenoxazine-4,11-disulfonic acid
  参考文献：
  名称：

  HENK, HERMANN;HARMS, WOLFGANG;WILD, PETER

  摘要：

  DOI：
• 作为产物：
  描述：

  Disodium;2-amino-5-[[4-(4-amino-3-sulfonatoanilino)-2,5-dichloro-3,6-dioxocyclohexa-1,4-dien-1-yl]amino]benzenesulfonate 生成 3,10-diamino-6,13-dichloro-[1,4]benzoxazino[2,3-b]phenoxazine-4,11-disulfonic acid
  参考文献：
  名称：

  RENFREW, A. H. M., J. SOC. DYERS AND COLOUR., 105,(1989) N-8, C. 262-264

  摘要：

  DOI：

文献信息

• ——
  作者：JAGER H.

  DOI：——

  日期：——
• Fiber-reactive compound having both pyridiniotriazinyl and vinylsulfone type groups
  申请人：SUMITOMO CHEMICAL COMPANY, LIMITED

  公开号：EP0167219B1

  公开（公告）日：1988-09-28
• DYES, THEIR PREPARATION AND USE IN THE COLORATION OF SUBSTRATES
  申请人：BASF AKTIENGESELLSCHAFT

  公开号：EP0639237B1

  公开（公告）日：1997-06-04
• TRIPHENDIOXAZINE DYESTUFFS FOR DYEING ORGANIC SUBSTRATES
  申请人：Clariant Finance (BVI) Limited

  公开号：EP1066340B1

  公开（公告）日：2002-07-24
• REACTIVE DYES, PROCESSES FOR THEIR PREPARATION AND THEIR USE
  申请人：Tzikas Athanassios

  公开号：US20100251490A1

  公开（公告）日：2010-10-07

  Reactive dyes of the formula (1) in which Q 1 is hydrogen, halogen or a radical of the formula R 1 , R 2 and R 3 independently of one another are hydrogen or C 1 -C 4 alkyl which is unsubstituted or substituted by hydroxyl, sulfo, carboxyl or sulfato, and R 1 in formula (1) and R 1 in formula (2a) have identical or different meanings and R 2 in formula (1) and R 2 in formula (2a) have identical or different meanings, (R 4 ) 0-1 and (R 5 ) 0-1 independently of one another are 0 or 1 identical or different substituents from the group consisting of C 1 -C 4 alkyl, C 1 -C 4 alkoxy, halogen and sulfo, A is hydrogen or C 1 -C 4 alkyl which is unsubstituted or substituted by hydroxyl, sulfo, carboxyl or sulfato, phenyl which is unsubstituted or substituted by C 1 -C 4 alkyl, C 1 -C 4 alkoxy, C 2 -C 4 alkanoylamino, hydroxyl, carboxyl, carbamoyl, sulfo or halogen, phenyl-C 1 -C 2 alkylene which is unsubstituted or substituted in the phenyl ring by C 1 -C 4 alkyl, C 1 -C 4 alkoxy, C 2 -C 4 alkanoylamino, hydroxyl, carboxyl, sulfo, carbamoyl or halogen, or C 5 -C 7 cycloalkyl which is unsubstituted or substituted by C 1 -C 4 alkyl, B is a C 2 -C 12 alkylene radical which can be interrupted by 1, 2 or 3 members from the group consisting of —NH—, —N(CH 3 )— or —O— and is unsubstituted or substituted by hydroxyl, sulfo, sulfato, cyano or carboxyl, a C 5 -C 7 cycloalkylene radical or C 1 -C 2 alkylene-C 5 -C 7 cycloalkylene radical which are unsubstituted or substituted in the cycloalkylring by C 1 -C 4 alkyl, C 1 -C 2 alkylenephenylene radical or phenylene radical which are unsubstituted or substituted in the phenyl ring by C 1 -C 4 alkyl, C 1 -C 4 alkoxy, C 2 -C 4 alkanoylamino, sulfo, halogen or carboxyl, V 1 and V 2 independently of one another are halogen, T is a radical of the formula —CO—(CH 2 ) m SO 2 —Y   (3a), —CO—CH(Hal)—CH 2 —Hal   (3b) or —CO—C(Hal)=CH 2 (3c), Hal is halogen, X is hydroxyl or Y, Y is vinyl or a radical —CH 2 —CH 2 —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.