摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

N-正丁基-N-羟基苯胺 | 78636-73-4

中文名称
N-正丁基-N-羟基苯胺
中文别名
——
英文名称
N-n-butyl-N-hydroxyaniline
英文别名
N-butyl-N-phenyl-hydroxylamine;N-Hydroxy-N-Butylanilin;N-butyl-N-phenylhydroxylamine
N-正丁基-N-羟基苯胺化学式
CAS
78636-73-4
化学式
C10H15NO
mdl
——
分子量
165.235
InChiKey
CXZVPMKLJRYLSU-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):
    2.8
  • 重原子数:
    12
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    23.5
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

点击查看最新优质反应信息

文献信息

  • Synthesis, characterization and photo physical-theoretical analysis of D-π-A compounds. 2. Chain length effect through even-odd effect on the photophysical properties
    作者:E. Ortega、A. Ramirez、L. Cattin、F.R. Díaz、M.A. del Valle、J.C. Bernède
    DOI:10.1016/j.dyepig.2017.07.069
    日期:2017.12
    but with different substituent, were synthesized. It is shown that the chain-size of the substituent group modifies the quantum yield. The news substituents introduced are a propyl (M8-3), butyl (M8-4), pentyl (M8-5) or hexyl (M8-6) group. In general, it was possible to see that the new substituents were able to increase their performances. Furthermore, an odd-even substituent effect, between propyl/pentyl
    在不断寻找用于太阳能设备的新化合物时,具有共轭桥连接的施主(D)和受主(A)电荷的偶极D-π-A分子家族一直是人们关注的焦点。近年来由于它们的不同特性。如前所述,基于叔不对称胺的分子几何形状与其量子产率之间存在联系。在当前工作中,基于相同主链分子的四个新化合物((E)-2-基-3-(5-((E)-2-(9,9-二乙基-7-(苯基基)-9 H合成了具有不同取代基的-(-2-基)乙烯基噻吩-2-基)丙烯酸)。结果表明,取代基的链大小改变了量子产率。引入的新闻取代基是丙基(M8-3),丁基(M8-4),戊基(M8-5)或己基(M8-6)。通常,可以看到新的取代基能够提高其性能。此外,发现丙基/戊基和丁基/己基之间的奇偶取代作用,并且理论几何数据能够顺应趋势。然而,理论上,该取代基的效果是在M8-3和M8-4的情况下,这可能是由于在激发态下接近450纳米(的发射图案的消失在λ反相2),如实验数据所示。最合适的行为属于[[
  • [EN] DENTAL COMPOSITION<br/>[FR] COMPOSITION DENTAIRE
    申请人:DENTSPLY DETREY GMBH
    公开号:WO2020127380A1
    公开(公告)日:2020-06-25
    Described herein is a dental composition containing a polymerizable compound having at least one optionally derivatized β-hydroxy urethane unit. The polymerizable compound having at least one optionally derivatized β-hydroxy urethane unit is obtained without use of organo-metal catalysts and isocyanates and by a reaction between an at least one component A having at least one cyclic carbonate group with an at least one component B having at least one of primary amine functional group and secondary amine functional group. The present disclosure relates to use of the polymerizable compound having at least one optionally derivatized β-hydroxy urethane unit for the preparation of a dental composition, in particular a dental composite, a glass ionomer, a dental cement, a dental sealant, and a dental adhesive.
    本文介绍了一种含有至少一个可选衍生化β-羟基基单元的可聚合化合物的牙科组合物。该可聚合化合物至少具有一个可选衍生化β-羟基基单元,其不使用有机属催化剂和异氰酸酯,通过至少一种具有至少一个环状碳酸酯基团的组分A与至少一种具有至少一个一级胺官能团和二级胺官能团的组分B之间的反应获得。本公开涉及使用具有至少一个可选衍生化β-羟基基单元的可聚合化合物制备牙科组合物,特别是牙科复合材料、玻璃离子体、牙科泥、牙科密封剂和牙科粘合剂。
  • Methods for making dental restorations using two-phase light-curing materials
    申请人:Sun Fuming
    公开号:US20080220396A1
    公开(公告)日:2008-09-11
    Methods for making dental crowns, bridges, inlays, onlays, veneers, fillings, and other restorations are provided. The methods involve using a two-phase light curing (TPLC) material. Preferably, the TPLC material used to form the dental restoration comprises a blend of polymerizable compounds; photopolymerization systems (a) and (b), and particulate filler materials (a) and (b). In a first light-curing step, curing light having a wavelength of greater than 420 nm is used to activate system (a). In a second light-curing step, curing light having a wavelength of less than 420 nm is used to activate system (b). The two step light-curing method is efficient and allows the dentist to make restorations having high mechanical strength and pleasing aesthetics.
    提供了制作牙冠、牙桥、嵌体、半嵌体、贴面、充填和其他修复的方法。该方法涉及使用两相光固化(TPLC)材料。优选地,用于形成牙科修复的TPLC材料包括可聚合化合物的混合物;光聚合系统(a)和(b),以及颗粒填料材料(a)和(b)。在第一次光固化步骤中,使用波长大于420nm的固化光来激活系统(a)。在第二个光固化步骤中,使用波长小于420nm的固化光来激活系统(b)。这种两步光固化方法高效,并允许牙医制作具有高机械强度和美观外观的修复。
  • METHODS FOR MAKING DENTAL RESTORATIONS USING TWO-PHASE LIGHT-CURING MATERIALS
    申请人:Sun Fuming
    公开号:US20110183298A1
    公开(公告)日:2011-07-28
    Methods for making dental crowns, bridges, inlays, onlays, veneers, fillings, and other restorations are provided. The methods involve using a two-phase light curing (TPLC) material. Preferably, the TPLC material used to form the dental restoration comprises a blend of polymerizable compounds; photopolymerization systems (a) and (b), and particulate filler materials (a) and (b). In a first light-curing step, curing light having a wavelength of greater than 420 nm is used to activate system (a). In a second light-curing step, curing light having a wavelength of less than 420 nm is used to activate system (b). The two step light-curing method is efficient and allows the dentist to make restorations having high mechanical strength and pleasing aesthetics.
    提供制作牙冠、牙桥、嵌体、面层、填充和其他修复的方法。这些方法涉及使用双相光固化(TPLC)材料。优选地,用于形成牙科修复的TPLC材料包括聚合化合物的混合物;光聚合系统(a)和(b),以及颗粒填料材料(a)和(b)。在第一次光固化步骤中,使用波长大于420 nm的固化光来激活系统(a)。在第二次光固化步骤中,使用波长小于420 nm的固化光来激活系统(b)。这种双步光固化方法高效,并允许牙医制作具有高机械强度和美观外观的修复物。
  • HIGH STRENGTH DENTAL MATERIAL
    申请人:SUN BENJAMIN J.
    公开号:US20120129973A1
    公开(公告)日:2012-05-24
    The invention provides a high strength dental composition including polymerizable dental resins. The dental composition is useful as restorative material and for making various dental devices, such as artificial teeth, crowns and bridges of high strength dental polymeric material.
    本发明提供了一种高强度的牙科组合物,包括可聚合的牙科树脂。该牙科组合物可用作修复材料,并用于制造各种高强度牙科聚合材料的人工牙齿,冠和桥。
查看更多