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methyl 3-(5-trifluoromethyl-2H-benzotriazol-2-yl)-5-tert-butyl-4-hydroxy-hydrocinnamate | 286471-12-3

中文名称
——
中文别名
——
英文名称
methyl 3-(5-trifluoromethyl-2H-benzotriazol-2-yl)-5-tert-butyl-4-hydroxy-hydrocinnamate
英文别名
Methyl 3-[3-tert-butyl-4-hydroxy-5-[5-(trifluoromethyl)benzotriazol-2-yl]phenyl]propanoate
methyl 3-(5-trifluoromethyl-2H-benzotriazol-2-yl)-5-tert-butyl-4-hydroxy-hydrocinnamate化学式
CAS
286471-12-3
化学式
C21H22F3N3O3
mdl
——
分子量
421.419
InChiKey
JMGAGEUAMQQJAD-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):
    5.6
  • 重原子数:
    30
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    77.2
  • 氢给体数:
    1
  • 氢受体数:
    8

文献信息

  • [EN] WATER COMPATIBLE STERICALLY HINDERED ALKOXYAMINES AND HYDROXY SUBSTITUTED ALKOXYAMINES<br/>[FR] ALCOXYAMINES STERIQUEMENT ENCOMBREES ET ALCOXYAMINES HYDROXY SUBSTITUEES HYDROCOMPATIBLES
    申请人:CIBA SC HOLDING AG
    公开号:WO2004076419A1
    公开(公告)日:2004-09-10
    Sterically hindered alkoxyamine and hydroxy substituted alkoxyamine stabilizer compounds are made water compatible via certain backbones with affinity towards water. The sterically hindered amines are for example of the formula where for example E and E’ are 2-hydroxycydohexyloxy, 2-hydroxy-2-methylpropoxy, benzyloxy, methoxy, propoxy, hexyloxy, heptyloxy, oclyloxy or cyclohexyloxy, Rx is for example -NH2+CH2CH20H Cl-, -NH3+ -OAc, =NOH, -NHCH(CH3)COO-K+,- NHCH2CH2NH(CH3)2+ -OAC, -NHCH2CH2SO3-K+, -NHCH(COO- K+)CH2CH2SCH3, -NHCH2COO- K+, -OCH(CH3)COO-K+, -OCH2CH2NH(CH3)2+ -OAC, -OCH2CH2SO3-K+, -OCH(COO- K+)CH2CH2SCH3 or -OCH2COO-K+, and where R5 comprises repeating units of -(OCH2CH2)-, -(OCH2CH2(CH3))-,-(CH2CHCOOH)-, -(CH2C(CH3)COOH)-, -(CH2CHCOOCH3)-, -(NHCH2CH2)-, -(CH2CHOH)-, -(CH2CHCONH2)-or -(CH2CH(NHCOH))-. These compounds are particularly effective in stabilizing aqueous polymer systems against the deleterious effects of oxidative, thermal and actinic radiation. The compounds are effective for example in stabilizing water borne coatings, aqueous inks, aqueous inkjet media and photocured aqueous systems.
    通过具有亲性的特定骨架,使具有立体位阻的烷氧胺和羟基取代的烷氧胺稳定剂化合物与相容。其中,立体位阻胺的示例为以下公式,其中 E 和 E’ 为 2-羟基环己氧基、2-羟基-2-甲基丙氧基、苄氧基、甲氧基、丙氧基、己氧基、庚氧基、辛氧基或环己氧基,Rx 为例如 -NH2+CH2CH20H Cl-, -NH3+ -OAc, =NOH, -NHCH(CH3)COO-K+,- NHCH2CH2NH( )2+ -OAC, -NHCH2CH2SO3-K+, -NHCH(COO- K+)CH2CH2S , -NHCH2COO- K+, -OCH( )COO-K+, -OCH2CH2NH( )2+ -OAC, -OCH2CH2SO3-K+, -OCH(COO- K+)CH2CH2S 或 -OCH2COO-K+,R5 包括重复单元 -(OCH2CH2)-, -(OCH2CH2( ))-,-(CH2CHCOOH)-, -(CH2C( )COOH)-, -(CH2CHCOO )-, -(NHCH2CH2)-, -(CH2CHOH)-, -(CH2CHCONH2)- 或 -(CH2CH(NHCOH))-. 这些化合物在稳定性聚合物体系抵抗氧化、热和光辐射的有害影响方面特别有效。这些化合物例如在稳定性涂料、性油墨、性喷墨介质和光固化性系统方面非常有效。
  • Benzotriazoles containing phenyl groups substituted by heteroatoms and compositions stabilized therewith
    申请人:——
    公开号:US20030004235A1
    公开(公告)日:2003-01-02
    2H-Benzotriazole UV absorbers substituted at the 3-position and/or the 5-position of the phenyl ring by a phenyl moiety which is substituted by a heteroatom are particularly photostable in automotive coatings, and are of low color and exhibit low volatility in thermoplastic compositions.
    3-位和/或5-位被苯基环上的苯基取代的2H-苯并三唑紫外线吸收剂,其被异原子取代的苯基特别在汽车涂料中具有光稳定性,并且在热塑性复合材料中具有低色度和低挥发性。
  • Processes for the preparation of benzotriazole UV absorbers
    申请人:——
    公开号:US20020035175A1
    公开(公告)日:2002-03-21
    Provided is a process for preparing 2H-benzotriazole UV absorbers containing a perfluoroalkyl moiety at the 5-position of the benzo ring, for example a trifluoromethyl group, which involves diazotizing the perfluoroalkyl substituted o-nitroaniline using concentrated sulfuric acid plus sodium nitrite or nitrosylsulfuric acid to form the corresponding monoazobenzene intermediate via the diazonium salt intermediate which is reduced to the corresponding 5-perfluoroalkyl substituted 2H-benzotriazole UV absorber compound by conventional reduction means. Also provided is a novel one-pot, multiphase reaction for the preparation of 2(2-nitrophenylazo) substituted phenols, which are precursors for 2H-benzotriazole UV absorbers.
    提供了一种制备在苯环的5位含有全氟烷基基团(例如三甲基基团)的2H-苯并三唑紫外吸收剂的方法,该方法涉及使用浓硫酸硝酸钠亚硝基硫酸制备全氟烷基取代的邻硝基苯胺,以形成相应的单氮偶联苯中间体,通过传统还原手段将二氮盐中间体还原为相应的5-全氟烷基取代的2H-苯并三唑紫外吸收剂化合物。还提供了一种用于制备2(2-硝基苯基偶氮)取代的新型一锅多相反应,这些化合物是2H-苯并三唑紫外吸收剂的前体。
  • Quinophenanthrine diones fluorescent whitening agents
    申请人:Cole Thurber Damien
    公开号:US20070050927A1
    公开(公告)日:2007-03-08
    Tetrahydro- and dihydroquinophenanthrine dione fluorescent whitening agents and a process for their preparation are provided.
    提供了四氢-和二氢喹诺酚酞荧光增白剂及其制备方法。
  • Carboxylic acid esters of zosteric acid for prevention of biofouling
    申请人:Elder Todd Stewart
    公开号:US20070128151A1
    公开(公告)日:2007-06-07
    Carboxylic acid ester derivatives of zosteric acid are effective in preventing biofouling and are readily formulated into coatings or films. Coating or film compositions of the esters, and methods for their application, are provided which reduce the dissolution of the esters into water or loss to the environment. The Zosteric acid esters of the invention appear to function by preventing adhesion of an organism to a surface rather than by acute toxic activity rendering said compositions more environmentally acceptable.
    Zosteric酸的羧酸酯衍生物在防止生物污垢方面非常有效,并且很容易制成涂层或薄膜。本发明提供了酯的涂层或薄膜组合物以及其应用方法,其减少了酯在中的溶解或对环境的损失。本发明的Zosteric酸酯似乎通过防止生物附着在表面上而不是通过急性毒性活性来发挥作用,从而使这些组合物更具环境可接受性。
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