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4-十二烷基-2-硝基苯胺 | 3663-32-9

中文名称
4-十二烷基-2-硝基苯胺
中文别名
——
英文名称
n-dodecyl-4 nitro-2 aniline
英文别名
4-n-dodecyl-2-nitroaniline;2-nitro-4-dodecylaniline;2-nitro-4n-dodecylaniline;4-dodecyl-2-nitro-aniline;4-Dodecyl-2-nitro-anilin;4-Dodecyl-2-nitroaniline
4-十二烷基-2-硝基苯胺化学式
CAS
3663-32-9
化学式
C18H30N2O2
mdl
——
分子量
306.448
InChiKey
NIVIDLVBSALQMX-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):
    7.8
  • 重原子数:
    22
  • 可旋转键数:
    11
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    71.8
  • 氢给体数:
    1
  • 氢受体数:
    3

安全信息

  • 海关编码:
    2921420090

SDS

SDS:9817a72946d724b7f333fc08a5866e0e
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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:
    4-十二烷基-2-硝基苯胺 在 palladium on activated charcoal 盐酸氢气 作用下, 以 甲醇 为溶剂, 25.0~130.0 ℃ 、101.33 kPa 条件下, 反应 18.0h, 生成 5-Dodecyl-2-methylsulfanylmethyl-1H-benzoimidazole; hydrochloride
    参考文献:
    名称:
    Krati, Noureddine; Roizard, Denis; Brembilla, Alain, Bulletin de la Societe Chimique de France, 1989, # 3, p. 443 - 448
    摘要:
    DOI:
  • 作为产物:
    描述:
    N-(4-十二烷基苯基)乙酰胺氢氧化钾硝酸乙酸酐 作用下, 以 乙醇溶剂黄146 为溶剂, 反应 7.0h, 生成 4-十二烷基-2-硝基苯胺
    参考文献:
    名称:
    Krati, Noureddine; Roizard, Denis; Brembilla, Alain, Bulletin de la Societe Chimique de France, 1989, # 3, p. 443 - 448
    摘要:
    DOI:
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文献信息

  • 4-higher alkyl-2-nitro-2'-hydroxy-3',5'-di-higher alkyl (or
    申请人:Ciba-Geigy Corporation
    公开号:US04847367A1
    公开(公告)日:1989-07-11
    4-Higher alkyl-2-nitro-2'-hydroxy-3',5'-di-higher alkyl (or cumyl)-azobenzenes are made by coupling the corresponding diazotized 4-higher alkyl-o-nitroaniline with the corresponding substituted phenol. These azobenzene intermediates are used to prepare the corresponding 2H-benzotriazole UV absorber stabilizers substituted on the 5-position of the benzo ring by a higher alkyl group, preferably tert-octyl or n-dodecyl.
    通过将相应的重链烷基-2-硝基-2'-羟基-3',5'-双重链烷基(或叔丁基)-偶氮苯与相应的取代酚偶联制备4-重链烷基-o-硝基苯胺重链烷基-2H-苯并三唑紫外线吸收剂稳定剂的中间体。这些偶氮苯中间体用于制备通过重链烷基(最好是叔辛基或正十二烷基)取代苯环5位的相应2H-苯并三唑紫外线吸收剂稳定剂。
  • Azo compound suitable for use in non-linear optics
    申请人:Imperial Chemical Industries PLC
    公开号:US05047516A1
    公开(公告)日:1991-09-10
    An azo compound of the formula: ##STR1## wherein R is an non-hydrophilic aliphatic or cycloaliphatic group containing from 8 to 40 carbon atoms; m is 0 or 1; R.sup.1 is NO.sub.2, CN or COOR.sup.2 ; R.sup.2 is H or C.sub.1-4 -alkyl; n is from 1 to 4 and R.sup.3 is H, a metal or a group containing a tetravalent N atom. The compound has non-linear optical properties which make it suitable for use in an optical element such as a waveguide, for altering the characteristics of light passing through the element.
    该化合物的偶氮化合物的式子为:##STR1## 其中R是一个含有8到40个碳原子的非亲水的脂肪族或环脂族基团;m为0或1;R.sup.1为NO.sub.2,CN或COOR.sup.2;R.sup.2为H或C.sub.1-4-烷基;n为1到4,R.sup.3为H,金属或含有四价N原子的基团。该化合物具有非线性光学性质,使其适用于用于光学元件,如波导,以改变通过元件的光的特性。
  • 5-Higher alkyl substituted-2H-benzotriazoles in stabilized compositions
    申请人:Ciba-Geigy Corporation
    公开号:US04904712A1
    公开(公告)日:1990-02-27
    5-tert-Octyl-2-(2-hydroxy-3,5-di-alpha-cumylphenyl)-2H-benzotriazole and related 2H-benzotriazoles substituted on the 5-position of the benzo ring by a higher alkyl group such as tert-octyl or dodecyl exhibit outstanding efficacy in protecting organic substrates from light-induced deterioration as well as good resistance to loss by volatilization or exudation during the high temperature processing of stabilized compositions. The above-named compounds exhibit good solubility in common organic solvents, and exhibit very high extinction coefficients.
    5-叔丁基-2-(2-羟基-3,5-二α-叔丙基苯基)-2H-苯并三唑及其在苯环的5位被高碳烷基如叔辛基或十二烷基取代的相关2H-苯并三唑,表现出在保护有机基质免受光引起的恶化方面的杰出功效,同时在稳定组合物高温加工期间不易挥发或渗出。上述化合物在常见有机溶剂中具有良好的溶解度,并表现出非常高的消光系数。
  • Optical element having non-linear optical properties
    申请人:Imperial Chemical Industries PLC
    公开号:US04981612A1
    公开(公告)日:1991-01-01
    An optical element, such as a wave guide, having non-linear optical properties, suitable for use in optical devices in which it is desirable to alter the characteristics of the light, comprising a transparent or reflecting substrate having at least a partial superficial coating comprising alternating monolayers of a first non-linear optical (NLO) compound of the formula: ##STR1## wherein R is an non-hydrophilic aliphatic or cycloaliphatic group containing from 8 to 40 carbon atoms; m is 1 or 2; R.sup.1 is NO.sub.2, CN or COOR.sup.2 ; R.sup.2 is H or C.sub.1-4 -alkyl; n is from 1 to 4; and R.sup.3 is H, a metal or a group containing a tetravalent N atom and a second NLO compound of the formula: ##STR2## wherein T is H, a metal or a group containing a tetravalent N atom; X is S, O, ##STR3## T.sup.1 is NO.sub.2, CN or COOY; Y is selected from H, C.sub.1-4 -alkyl, a metal or a group containing a tetravalent N atom; T.sup.2 and T.sup.3 are each independently H or a non-hydrophilic aliphatic or cycloaliphatic group containing up to 30 carbon atoms; T.sup.4 and T.sup.5 are each independently H or a non-hydrophilic aliphatic or cycloaliphatic group containing up to 30 carbon atoms; and T.sup.6 and T.sup.7 are each independently H or a non-hydrophilic group containing up to 4 carbon atoms; or T.sup.4 and T.sup.6 together comprise ring fused to Ring A and T.sup.5 and T.sup.7 are as hereinbefore defined; or T.sup.5 and T.sup.7 together comprise ring fused to Ring A and T.sup.4 and T.sup.6 are as hereinbefore defined; or T.sup.2 and T.sup.4 together with the N atom to which T.sup.2 is attached form a ring fused to Ring A and T.sup.3 and T.sup.5 are as hereinbefore defined; or T.sup.3 and T.sup.5 together with the N atom to which T.sup.3 is attached form a ring fused to Ring A and T.sup.2 and T.sup.4 are as hereinbefore defined; provided there are, in total, from 8 to 40 carbon atoms in one or two of the groups independently represented by T.sup.2, T.sup.3, T.sup.4 and T.sup.5.
    一种具有非线性光学性质的光学元件,例如波导,适用于希望改变光特性的光学设备,包括具有至少部分表面涂层的透明或反射基底,该表面涂层由第一种非线性光学(NLO)化合物的交替单层组成,该化合物的化学式为:其中R是含有8到40个碳原子的非亲水脂肪族或环烷基;m为1或2;R1为NO2,CN或COOR2;R2为H或C1-4-烷基;n为1到4;R3为H,金属或含有四价N原子的基团;以及第二种NLO化合物,其化学式为:其中T为H,金属或含有四价N原子的基团;X为S、O、或;T1为NO2,CN或COOY;Y选择自H、C1-4-烷基、金属或含有四价N原子的基团;T2和T3分别独立地为H或含有高达30个碳原子的非亲水脂肪族或环烷基;T4和T5分别独立地为H或含有高达30个碳原子的非亲水脂肪族或环烷基;T6和T7分别独立地为H或含有高达4个碳原子的非亲水基团;或T4和T6一起构成与环A螺合的环,T5和T7如前所述;或T5和T7一起构成与环A螺合的环,T4和T6如前所述;或T2和T4与T2连接的N原子一起形成与环A螺合的环,T3和T5如前所述;或T3和T5与T3连接的N原子一起形成与环A螺合的环,T2和T4如前所述;只要在由T2、T3、T4和T5独立表示的一个或两个组中总共有8到40个碳原子。
  • 5-Higher alkyl substituted-2H-benzotriazoles
    申请人:Ciba-Geigy Corporation
    公开号:US04727158A1
    公开(公告)日:1988-02-23
    5-tert-Octyl-2-(2-hydroxy-3,5-di-alpha-cumylphenyl)-2H-benzotriazole and related 2H-benzotriazoles substituted on the 5-position of the benzo ring by a higher alkyl group such as tert-octyl or dodecyl exhibit outstanding efficacy in protecting organic substrates from light-induced deterioration as well as good resistance to loss by volatilization or exudation during the high temperature processing of stabilized compositions. The above-named compounds exhibit good solubility in common organic solvents, and exhibit very high extinction coefficients.
    5-叔丁基-2-(2-羟基-3,5-二α-叔丁基苯基)-2H-苯并三唑及其在苯环的5位被高碳烷基取代的类似2H-苯并三唑,如叔辛基或十二烷基,表现出在保护有机基质免受光致劣化方面的杰出效果,同时在稳定组合物的高温处理期间具有很好的抗挥发或渗出性能。上述化合物在常见有机溶剂中具有良好的溶解性,并表现出非常高的消光系数。
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