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disperse orange 3 | 70734-98-4

中文名称
——
中文别名
——
英文名称
disperse orange 3
英文别名
——
disperse orange 3化学式
CAS
70734-98-4
化学式
C12H10N4O2
mdl
——
分子量
242.237
InChiKey
UNBOSJFEZZJZLR-CCEZHUSRSA-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):
    3.59
  • 重原子数:
    18.0
  • 可旋转键数:
    3.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    93.88
  • 氢给体数:
    1.0
  • 氢受体数:
    5.0

SDS

SDS:891ed73fb7a73e92394174a62c95dba6
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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
  • 下游产品
    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:
    disperse orange 3 在 sodiumsulfide nonahydrate 、 sodium nitrite 作用下, 以 乙醇 为溶剂, 反应 0.75h, 生成 4-(4-azulen-1-ylazophenyl)azoaniline
    参考文献:
    名称:
    Extended aromatic π-electron conjugated dyes with three azo bonds and either one or two azulen-1-yl moieties in molecule. Synthesis and basicity
    摘要:
    Azo dyes with either one or two identical or different azulen-1-yl moieties attached to the structure -N-2-C6H4-N-2-C6H4-N-2- were prepared, the phenylene ring being either 1,3-1'3' or 1,4-1',4' disubstituted. The syntheses were accomplished in good yields via mono or bis diazotization of the corresponding anilines followed by the coupling with unsubstituted or alkyl substituted azulenes in acetic/acetate medium. The recorded electronic spectra of the synthesized compounds were analyzed and were compared with those of related compounds. The isosbestic points resulting from protonation of the azo compounds enabled pK(a) values to be determined. From these pK(a) values it is apparent that all studied compounds are very weak bases. The high solvatochromic property of the compounds with para,para-substituted phenylene groups reflects the hyperpolarizability of these compounds. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.dyepig.2011.08.002
  • 作为产物:
    描述:
    4-(4-硝基苯基偶氮)苯胺 以 正庚烷 为溶剂, 生成 disperse orange 3
    参考文献:
    名称:
    Rate constants of the thermal cis-trans isomerization of azobenzene dyes in solvents, acetone/water mixtures, and in microheterogeneous surfactant solutions
    摘要:
    Rate constants k(iso) of the thermal cis-trans isomerization of four 4,4'-nitro-aminoazobenzenes with different amino groups have been determined in homogeneous aprotic solvents and polyglykol oligomers, primarily by means of conventional flash photolysis. The rate constants have been correlated with polarity (according to lambda(max) from UV/Vis absorption spectra of the trans isomers) and bulk viscosity of the solvents. Qualitative conclusions about the influence of varying concentrations of water with respect to polarity and hydrogen banding on k(iso)- and lambda(max)-values in acetone/water mixtures were derived. Based on these results the data from microheterogeneous solutions have been interpreted.In microheterogeneous water/surfactant solutions k(iso)-values of selected azo dyes were strongly dependent on the concentrations of SDS, Triton(R) X-100, C12EO8 in water, and varied with the composition of bicontinuous microemulsions of Igepal(R) CA-520/ heptane/water. The large spread of isomerization rate constants is in part due to varying microviscosity.Replacement of H2O by D2O in aqueous surfactant solutions produced surprisingly large kinetic solvent isotope effects. (C) 1999 John Wiley & Sons, Inc.
    DOI:
    10.1002/(sici)1097-4601(1999)31:5<337::aid-kin3>3.0.co;2-e
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文献信息

  • COMPOSITIONS AND METHODS FOR DETECTING NERVE AGENTS
    申请人:Corcoran Robert C.
    公开号:US20100130757A1
    公开(公告)日:2010-05-27
    The present invention provides methods and compositions for detecting, identifying and measuring the abundance of chemical nerve agents. Methods and compositions of the present invention are capable of providing selective detection of phosphorous based nerve agents, such as nerve agents that are esters of methyl phosphonic acid derivatives incorporating a moderately good leaving group at the phosphorus. Selectivity in the present invention is provided by a sensor composition having an alpha (α) effect nucleophile group that undergoes specific nucleophilic substitution and rearrangement reactions with phosphorus based nerve agents having a tetrahederal phosphorous bound to oxygen. The present invention includes embodiments employing a sensor composition further comprising a reporter group covalently linked to the alpha effect nucleophile group allowing rapid optical readout of nerve agent detection events, including direct visual readout and optical readout via spectroscopic analysis.
    本发明提供了用于检测、识别和测量化学神经毒剂丰度的方法和组合物。本发明的方法和组合物能够选择性地检测基于磷的神经毒剂,例如酯化了在磷上具有中等良好离去基团的甲基膦酸衍生物的神经毒剂。本发明中的选择性是通过具有α效应亲核基团的传感器组合物提供的,该亲核基团与磷基神经毒剂发生特定的亲核取代和重排反应,其中磷与氧结合形成四面体磷。本发明包括采用传感器组合物的实施例,该传感器组合物进一步包括与α效应亲核基团共价连接的报告基团,允许对神经毒剂检测事件进行快速光学读数,包括直接视觉读数和通过光谱分析的光学读数。
  • Azobenzene-benzoylphenylureas as photoswitchable chitin synthesis inhibitors
    作者:Xue Tian、Chao Zhang、Qi Xu、Zhong Li、Xusheng Shao
    DOI:10.1039/c6ob02813f
    日期:——
    Benzoylphenylureas (BPUs) are used as synthetic insect growth regulators for inhibiting chitin synthesis. Merging insecticidal BPUs with photoswitchable azobenzene generated photoresponsive chitin synthesis inhibitors. A prepared azobenzene-benzoylphenylurea can be activated upon irradiation with UV light, and shows 6-fold and 2-fold activity difference to armyworm (Mythimna separata) and German cockroach
    苯甲酰基苯基脲(BPU)用作合成昆虫生长调节剂,可抑制甲壳质的合成。将杀虫性BPU与可光转换的偶氮苯合并可产生光响应性几丁质合成抑制剂。制备的偶氮苯-苯甲酰基苯基脲可在紫外光照射下被活化,与粘虫(Mythimna separata)和德国蟑螂(Blattella germanica)磺酰脲受体的活性分别相差6倍和2倍。这是光可切换的BPU杀虫剂的第一个例子。这种光响应性BPU杀虫剂的产生允许通过光调节杀虫活性,并且可以促进对磺酰脲受体的时空控制和这种杀虫剂的机理研究。
  • COLORING AGENTS AND METHODS OF USE THEREOF
    申请人:Living Proof, Inc.
    公开号:US20160106648A1
    公开(公告)日:2016-04-21
    Dyes, compositions comprising dyes and methods for using the same are provided.
    染料、包含染料的组合物以及使用这些染料的方法。
  • Signalling Mechanisms in Anion-Responsive Push-Pull Chromophores: The Hydrogen-Bonding, Deprotonation and Anion-Exchange Chemistry of Functionalized Azo Dyes
    作者:José V. Ros-Lis、Ramón Martínez-Máñez、Félix Sancenón、Juan Soto、Knut Rurack、Hardy Weißhoff
    DOI:10.1002/ejoc.200601111
    日期:2007.5
    HSO4–, carboxylates such as acetate and benzoate and the linear anions cyanide and thiocyanate) were employed in the recognition studies. Two different effects were distinguished: (i) bathochromic shifts of <40 nm to pale orange, due to anion coordination, and (ii) strong red shifts of ca. 200 nm with a concomitant colour change to blue, due to deprotonation. This behaviour was explained as a balance between
    合成了一系列含有酰胺 (1)、尿素 (2)、硫脲 (3)、氨基甲酸酯 (4) 或氨基 (5) 氢键供体基团的偶氮染料,并研究了它们对阴离子的响应。1-5 的乙腈溶液显示亮黄色,这是由于 375-400 nm 区域的电荷转移带,受到连接到 4-硝基偶氮苯支架 4' 端的基团的电子供体强度的轻微调制。不同形状和大小的阴离子(即球形 F-、Cl-、Br- 和 I-,平面和四面体含氧阴离子如 NO3-、H2PO4- 和 HSO4-,羧酸盐如乙酸盐和苯甲酸盐以及线性阴离子氰化物和硫氰酸盐) 被用于识别研究。区分了两种不同的效果:(i)由于阴离子配位,<40 nm 的红移至浅橙色,以及(ii)约 40 nm 的强红移。由于去质子化,200 nm 伴随颜色变为蓝色。这种行为被解释为不同受体中结合位点的去质子化趋势与阴离子的质子亲和力之间的平衡。进行了半经验计算以评估阴离子和染料的氢键供体能力,并观察到与
  • Water-soluble polymeric dye
    申请人:DSM IP Assets B.V.
    公开号:EP1489144A1
    公开(公告)日:2004-12-22
    The invention relates to a water-soluble polymeric dye comprising an anionic or nonionic chromophore unit covalently bound to a polymer backbone, wherein the polymer backbone is based on a water-soluble anionic or nonionic polymer and the polymer backbone comprises a) at least 2.5 anionic functional groups or at least 5 hydroxyl functional groups, or a combination thereof, per average chromophore unit for an anionic chromophore unit or b) at least 3.5 anionic functional groups or at least 7 hydroxyl functional groups, or a combination thereof, per average chromophore unit, for an nonionic chromophore unit. The polymeric dye according to the invention has good skin and fabric washability, and can be applied in paints and ink formulations for use markers and ink jet cartridges.
    该发明涉及一种水溶性聚合物染料,包括一个阴离子或非离子色团单元与聚合物骨架共价结合,其中聚合物骨架基于水溶性阴离子或非离子聚合物,且聚合物骨架包括:a)每个阴离子色团单元至少2.5个阴离子功能基或至少5个羟基功能基,或其组合,对于阴离子色团单元;或b)每个非离子色团单元至少3.5个阴离子功能基或至少7个羟基功能基,或其组合,对于非离子色团单元。根据该发明的聚合物染料具有良好的皮肤和织物可洗性,并可应用于油漆和墨水配方中,用于标记笔和喷墨打印机墨盒。
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表征谱图

  • 氢谱
    1HNMR
  • 质谱
    MS
  • 碳谱
    13CNMR
  • 红外
    IR
  • 拉曼
    Raman
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cnmr
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  • 峰位数据
  • 峰位匹配
  • 表征信息
Shift(ppm)
Intensity
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Assign
Shift(ppm)
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测试频率
样品用量
溶剂
溶剂用量
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同类化合物

黑洞猝灭剂-2,BHQ-2ACID 麦角甾烷-6-酮,2,3,22,23-四羟基-,(2a,3a,5a,22S,23S,24S)- 颜料橙61 阿利新黄GXS 阳离子红X-GTL 阳离子红5BL 阳离子橙RN 阳离子橙GLH 间甲基红 镨(3+)丙烯酰酸酯 镍酸酯(1-),[3-羟基-4-[(4-甲基-3-硫代苯基)偶氮]-2-萘羧酸根(3-)]-,氢 钴,[二[m-[[1,2-二苯基-1,2-乙二酮1,2-二(肟酸根-kO)](2-)]]四氟二硼酸根(2-)-kN1,kN1',k2,kN2']-,(SP-4-1)- 钠5-氯-2-羟基-3-[(2-羟基-4-{[(4-甲基苯基)磺酰基]氧基}苯基)偶氮]苯磺酸酯 钠5-[[3-[[5-[[4-[[[4-[(4,5-二氢-3-甲基-5-氧代-1H-吡唑-4-基)偶氮]苯基]氨基]羰基]苯基]偶氮]-2,4-二羟基苯基]偶氮]-4-羟基苯基]偶氮]水杨酸盐 钠4-[(4-氨基苯基)偶氮]苯甲酸酯 钠4-[(4-{[4-(二乙基氨基)苯基]偶氮}苯基)偶氮]苯磺酸酯 钠4-({3-甲氧基-4-[(4-甲氧基苯基)偶氮]苯基}偶氮)苯磺酸酯 钠3-({5-甲氧基-4-[(4-甲氧基苯基)偶氮]-2-甲基苯基}偶氮)苯磺酸酯 重氮基烯,苯基[4-(三氟甲基)苯基]- 重氮基烯,[4-[(2-乙基己基)氧代]-2,5-二甲基苯基](4-硝基苯基)- 重氮基烯,(2-氯苯基)苯基- 酸性金黄G 酸性棕S-BL 酸性媒介棕6 酸性媒介棕48 酸性媒介棕4 酸性媒介棕24 邻氨基偶氮甲苯 达布氨乙基甲硫基磺酸盐 赛甲氧星 茴香酸盐己基 苯重氮化,2-甲氧基-5-甲基-4-[(4-甲基-2-硝基苯基)偶氮]-,氯化 苯酰胺,4-[4-(2,3-二氢-1,4-苯并二噁英-6-基)-5-(2-吡啶基)-1H-咪唑-2-基]- 苯胺棕 苯胺,4-[(4-氯-2-硝基苯基)偶氮]- 苯甲酸,2-[3-[4-(苯偶氮基)苯基]-1-三氮烯基基]- 苯基-(4-苯基偶氮苯基)二氮烯 苯基-(4-哌啶-1-基苯基)二氮烯 苯基-(4-吡咯烷-1-基苯基)二氮烯 苯乙酸,-α-,4-二甲基-,(-alpha-S)-(9CI) 苏丹红 苏丹橙G 苏丹Ⅳ 膦酸,[(2-羟基苯基)[[4-(苯偶氮基)苯基]氨基]甲基]-,二乙基酯 脂绯红 耐晒深蓝R盐 耐晒枣红GBC 羰基[苯基(丙烷-2-基)氨基]乙酸 美沙拉嗪杂质06 美沙拉嗪杂质05