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2-[2-[8-[(4,6-Dichloro-1,3,5-triazin-2-yl)amino]-1-hydroxy-3,6-disulfo-2-naphthalenyl]diazenyl]-1,5-naphthalenedisulfonic acid | 57583-84-3

中文名称
——
中文别名
——
英文名称
2-[2-[8-[(4,6-Dichloro-1,3,5-triazin-2-yl)amino]-1-hydroxy-3,6-disulfo-2-naphthalenyl]diazenyl]-1,5-naphthalenedisulfonic acid
英文别名
5-[(4,6-dichloro-1,3,5-triazin-2-yl)amino]-3-[(1,5-disulfonaphthalen-2-yl)diazenyl]-4-hydroxynaphthalene-2,7-disulfonic acid
2-[2-[8-[(4,6-Dichloro-1,3,5-triazin-2-yl)amino]-1-hydroxy-3,6-disulfo-2-naphthalenyl]diazenyl]-1,5-naphthalenedisulfonic acid化学式
CAS
57583-84-3
化学式
C23H14Cl2N6O13S4
mdl
——
分子量
781.567
InChiKey
FWZGNYWQIHQQMP-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    3.2
  • 重原子数:
    48
  • 可旋转键数:
    8
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    347
  • 氢给体数:
    6
  • 氢受体数:
    19

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    4-(-β-[sulphatoethyl]sulphonyl) chloroacetanilide 、 2-[2-[8-[(4,6-Dichloro-1,3,5-triazin-2-yl)amino]-1-hydroxy-3,6-disulfo-2-naphthalenyl]diazenyl]-1,5-naphthalenedisulfonic acidsodium hydrogensulfide 、 sodium carbonate 作用下, 以 为溶剂, 反应 4.5h, 以63%的产率得到5-[[4-Chloro-6-[2-oxo-2-[4-(2-sulfooxyethylsulfonyl)anilino]ethyl]sulfanyl-1,3,5-triazin-2-yl]amino]-3-[(1,5-disulfonaphthalen-2-yl)diazenyl]-4-hydroxynaphthalene-2,7-disulfonic acid
    参考文献:
    名称:
    The synthesis and application of novel 2-chloro-4-alkylthio triazinyl reactive dyes
    摘要:
    Two hetero bi-functional reactive dyes (red and yellow) each containing both a sulphatoethylsulphonyl and 2-chloro-4-alkylthio-s-triazinyl reactive group have been synthesised and their dyeing properties including exhaustion, colour strength on fabric (visual colour yield), fixation and wash fastness compared with market leading products. Under the alkaline application conditions employed, both the dyes, a yellow and a red, having a novel bridging group, exhibited good build-up, fixation and wet fastness properties being essentially comparable with leading commercial products. The concept of synthesising a substituent that can be introduced into a dye as a linking group to impart increased reactivity to a chlorotriazine has been demonstrated to be viable and effective. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.dyepig.2012.08.016
  • 作为产物:
    参考文献:
    名称:
    The synthesis and application of novel 2-chloro-4-alkylthio triazinyl reactive dyes
    摘要:
    Two hetero bi-functional reactive dyes (red and yellow) each containing both a sulphatoethylsulphonyl and 2-chloro-4-alkylthio-s-triazinyl reactive group have been synthesised and their dyeing properties including exhaustion, colour strength on fabric (visual colour yield), fixation and wash fastness compared with market leading products. Under the alkaline application conditions employed, both the dyes, a yellow and a red, having a novel bridging group, exhibited good build-up, fixation and wet fastness properties being essentially comparable with leading commercial products. The concept of synthesising a substituent that can be introduced into a dye as a linking group to impart increased reactivity to a chlorotriazine has been demonstrated to be viable and effective. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.dyepig.2012.08.016
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文献信息

  • The synthesis and application of novel 2-chloro-4-alkylthio triazinyl reactive dyes
    作者:Khalid Pasha、John A. Taylor
    DOI:10.1016/j.dyepig.2012.08.016
    日期:2013.2
    Two hetero bi-functional reactive dyes (red and yellow) each containing both a sulphatoethylsulphonyl and 2-chloro-4-alkylthio-s-triazinyl reactive group have been synthesised and their dyeing properties including exhaustion, colour strength on fabric (visual colour yield), fixation and wash fastness compared with market leading products. Under the alkaline application conditions employed, both the dyes, a yellow and a red, having a novel bridging group, exhibited good build-up, fixation and wet fastness properties being essentially comparable with leading commercial products. The concept of synthesising a substituent that can be introduced into a dye as a linking group to impart increased reactivity to a chlorotriazine has been demonstrated to be viable and effective. (C) 2012 Elsevier Ltd. All rights reserved.
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