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

tinuvin 479 | 304671-49-6

中文名称
——
中文别名
——
英文名称
tinuvin 479
英文别名
2-(2-hydroxy-4-{1-octyloxycarbonylethyloxy}-phenyl)-4,6-bis-(4-biphenylyl)-1,3,5-triazine;2-{2-hydroxy-4-[(octyloxycarbonyl)ethylideneoxy]phenyl}-4,6-Bis(4-biphenylyl)-1,3,5-triazine;octyl 2-[4-[4,6-bis(4-phenylphenyl)-1,3,5-triazin-2-yl]-3-hydroxyphenoxy]propanoate
tinuvin 479化学式
CAS
304671-49-6
化学式
C44H43N3O4
mdl
——
分子量
677.843
InChiKey
TWCBCCIODCKPGX-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):
    11.6
  • 重原子数:
    51
  • 可旋转键数:
    16
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.23
  • 拓扑面积:
    94.4
  • 氢给体数:
    1
  • 氢受体数:
    7

反应信息

  • 作为反应物:
    描述:
    tinuvin 479三羟甲基丙烷二正丁基氧化锡 作用下, 反应 5.0h, 以63%的产率得到2,2-Bis(hydroxymethyl)butyl 2-[4-[4,6-bis(4-phenylphenyl)-1,3,5-triazin-2-yl]-3-hydroxyphenoxy]propanoate
    参考文献:
    名称:
    Special UV absorbers for curable UV-protective coatings
    摘要:
    本发明涉及具有两个或更多聚合丙烯酸酯或甲基丙烯酸酯基团的有机紫外线吸收剂,涂料组合物包括这种紫外线吸收剂,以及由此制得的涂层和涂覆了这种涂层的基材。
    公开号:
    US09273213B2
  • 作为产物:
    描述:
    辛醇titanium(IV) isopropylatepotassium carbonate 作用下, 以 正辛烷丙酮 为溶剂, 反应 16.0h, 生成 tinuvin 479
    参考文献:
    名称:
    1,3,5-三嗪紫外线吸收剂CGL-479的简单合成方法及其表征
    摘要:
    作为一种新型的紫外线(UV)吸收剂,在2-{2-羟基-4-[[(辛氧基氧羰基)亚乙氧基]苯基} -4,6-双(4-联苯基)-中在UVA区域(320〜400 nm)中具有出色的性能。 1,3,5-三嗪(CGL-479)通过简单的方法分四个步骤合成,总收率为45.3%。其出色的紫外线吸收能力(λmax  = 326 nm,εmax  = 4.15×10 4  L•mol -1 •cm -1),高热稳定性[ T 5(重量损失5%的温度)= 385°C]以及与聚合物材料的相容性使其成为传统紫外线吸收剂的潜在替代品。
    DOI:
    10.1002/jhet.2026
点击查看最新优质反应信息

文献信息

  • Process for the synthesis of amine ethers from secondary amino oxides
    申请人:——
    公开号:US20030171461A1
    公开(公告)日:2003-09-11
    An amine ether of formula (A) wherein a is 1 or 2; and when a is 1, E is E′; when a is 2, E is L; E′ is C 1 -C 36 alkyl; C 3 -C 18 alkenyl; C 2 -C 18 alkinyl; C 5 -C 18 cycloalkyl; C 5 -C 18 cycloalkenyl; a radical of a saturated or unsaturated aliphatic bicyclic or bricyclic hydrocarbon of 7 to 12 carbon atoms; C 2 -C 7 alkyl or C 3 -C 7 alkenyl substituted by halogen; C 7 -C 15 aralkyl or C 7 -C 15 aralkyl substituted by C 1 -C 4 alkyl or phenyl; or E′ is a radical of formula (VII) as explained in claim 1; T′ is tertiary C 4 -C 18 alkyl or phenyl, each of which are unsubstituted or substituted by halogen, OH, COOR 21 or C(O)—R 22 ; or T′ is C 5 -C 12 cycloalkyl; C 5 -C 12 cacloalkyl which is interrupted by at least one O or —NR 18 —; a polycyclic alkyl radical having 7-18 carbon atoms, or the same radical which is interrupted by at least one O or —NR 18 —; or T′ is —C(G 1 )(G 2 )—T″; or C 1 -C 18 alkyl or C 5 -C 12 cycloalkyl substituted by F(I)T″ is hydrogen, halogen, NO 2 , cyano, or is a monovalent organic radical comprising 1-50 carbon atoms; or T″ and T′ together form a divalent organic linking group completing, together with the hindered amine nitrogen atom and the quaternary carbon atom substituted by G 1 and G 2 , an optionally substituted five- or six-membered ring structure; and all other residues are as defined in claim 1, are obtained in good yield from the corresponding N-oxyl hindered amine precursor by reaction with a hydrocarbon E 1 —H or H—L—H in the presence of an organic hydroperoxide and a catalytic amount of copper or a copper compound. The products of present process find utility as polymerization regulators and/or light stabilizers for organic material.
    公式(A)的胺醚式化合物,其中a为1或2;当a为1时,E为E′;当a为2时,E为L;E′为C1-C36烷基;C3-C18烯基;C2-C18炔基;C5-C18环烷基;C5-C18环烯基;具有7到12个碳原子的饱和或不饱和脂肪环二元或三元碳氢化合物的基团;被卤素取代的C2-C7烷基或C3-C7烯基;C7-C15芳基烷基或C7-C15芳基烷基被C1-C4烷基或苯基取代;或E′为公式(VII)中所述的基团;T′为三级C4-C18烷基或苯基,其未被取代或被卤素、OH、COOR21或C(O)—R22取代;或T′为C5-C12环烷基;C5-C12环烷基被至少一个O或—NR18—打断;具有7-18个碳原子的多环烷基基团,或相同的基团,其被至少一个O或—NR18—打断;或T′为—C(G1)(G2)—T″;或被F(I)取代的C1-C18烷基或C5-C12环烷基,其中T″为氢、卤素、NO2基,或是由1-50个碳原子组成的一价有机基团;或T″和T′一起形成一个二价的有机连接基团,与受阻胺氮原子和被G1和G2取代的四价碳原子一起完成一个可选择取代的五元或六元环结构;所有其他残基如权利要求1所定义,通过在有机过氧化物和化合物的存在下与烃E1—H或H—L—H反应,从相应的N-氧代受阻胺前体中获得良好的收率。本方法的产物可用作有机材料的聚合物调节剂和/或光稳定剂
  • Synergistic UV absorber combination
    申请人:Ciba Specialty Chemicals Holding Inc.
    公开号:EP1308084A1
    公开(公告)日:2003-05-07
    A stabilizer composition comprising (A) a compound of the formula I wherein R is (CH2-CH2-O-)n-R2; -CH2-CH(OH)-CH2-O-R2; or -CH(R3)-CO-O-R4; n is 0 or 1; R2 is C1-C13alkyl or C2-C20alkenyl or C6-C12aryl or CO-C1-C18alkyl; R3 is H or C1-C8alkyl; R4 is C1-C12alkyl or C2-C12alkenyl or C5-C6cycloalkyl; and (B) one or more compounds selected from (i) to (xlv) as defined in claim 1 is especially effective towards stabilizing organic materials against degradation induced by light, heat or oxidation.
    一种稳定剂组合物,包括(A)式I的化合物,其中R为(CH2- -O-)n-R2;- -CH(OH)- -O-R2;或-CH(R3)-CO-O-R4;n为0或1;R2为C1-C13烷基或C2-C20烯基或C6-C12芳基或CO-C1-C18烷基;R3为H或C1-C8烷基;R4为C1-C12烷基或C2-C12烯基或C5-C6环烷基;以及(B)根据权利要求1所定义的(i)至(xlv)中的一种或多种化合物,对于稳定有机材料抵抗光、热或氧化引起的降解特别有效。
  • Curable composition and coated article
    申请人:Higuchi Koichi
    公开号:US20070212557A1
    公开(公告)日:2007-09-13
    A curable composition comprises (A) an organic/inorganic composite in which a hydrolyzable silyl group and/or SiOH group-containing polysiloxane is bonded to a vinyl polymer through a Si—C bond, and (B) an organic UV absorber having a molecular weight of at least 500 and a weight retentivity of at least 95% when held at 150° C. for 24 hours in an open state. The curable composition is coated and cured to an article, whereby the article is endowed with satisfactory weathering resistance while minimizing coloration or degradation.
    一种可治愈的组合物包括(A)一种有机/无机复合物,其中通过Si-C键将可解的基团和/或含有SiOH基团的聚硅氧烷乙烯基聚合物结合,和(B)一种分子量至少为500且在开放状态下保持150°C持续24小时时重量保留率至少为95%的有机紫外线吸收剂。将可治愈的组合物涂覆并固化到物品上,从而使物品在最小化着色或降解的同时具有令人满意的耐候性。
  • Flame retardant compositions
    申请人:Ronan Nicolas
    公开号:US20070029531A1
    公开(公告)日:2007-02-08
    The present invention is directed to a method of flame retarding a polymeric substrate using a specific group of azo and peroxide derivatives as flame retardants, to flame retardant compositions as well as to novel azo compounds usable as flame retarding compounds.
    本发明涉及一种使用特定的偶氮和过氧化物衍生物作为阻燃剂的聚合物基材的阻燃方法,以及阻燃组合物和可用作阻燃化合物的新型偶氮化合物。
  • VEHICLE MEMBER AND PROCESS FOR PRODUCING THE SAME
    申请人:Mitsuoka Tetsuya
    公开号:US20120244361A1
    公开(公告)日:2012-09-27
    Disclosed is a vehicle member comprising a resin substrate and a protective film formed on at least a part of the surface of the resin substrate. The protective film is produced by curing a curable coating agent composition, wherein the curable coating agent composition comprises 95 to 65 parts by mass of a component (A) comprising an urethane adduct compound having weather resistance, 5 to 35 parts by mass of a component (B) comprising a specific organosilicon compound, 0.1 to 10 parts by mass of a component (C) which is a radical polymerization initiator, 1 to 12 parts by mass of a component (D) which is an ultraviolet ray absorber, and 10 to 1,000 parts by mass of a component (E) which is an organic solvent, with respect to 100 parts by mass of the components (A) and (B) in total.
    公开了一种车辆部件,包括树脂基板和形成在树脂基板表面至少一部分的保护膜。所述保护膜是由可固化涂料剂组成制备而成,其中所述可固化涂料剂组成包括相对于总质量的组分(A)95至65质量份,所述组分(A)包括具有耐候性的加成物化合物,组分(B)5至35质量份,所述组分(B)包括特定的有机硅化合物,组分(C)0.1至10质量份,所述组分(C)是自由基聚合引发剂,组分(D)1至12质量份,所述组分(D)是紫外线吸收剂,组分(E)10至1000质量份,所述组分(E)是有机溶剂。
查看更多

同类化合物

(βS)-β-氨基-4-(4-羟基苯氧基)-3,5-二碘苯甲丙醇 (S,S)-邻甲苯基-DIPAMP (S)-(-)-7'-〔4(S)-(苄基)恶唑-2-基]-7-二(3,5-二-叔丁基苯基)膦基-2,2',3,3'-四氢-1,1-螺二氢茚 (S)-盐酸沙丁胺醇 (S)-3-(叔丁基)-4-(2,6-二甲氧基苯基)-2,3-二氢苯并[d][1,3]氧磷杂环戊二烯 (S)-2,2'-双[双(3,5-三氟甲基苯基)膦基]-4,4',6,6'-四甲氧基联苯 (S)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (R)富马酸托特罗定 (R)-(-)-盐酸尼古地平 (R)-(-)-4,12-双(二苯基膦基)[2.2]对环芳烷(1,5环辛二烯)铑(I)四氟硼酸盐 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[((6-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[(4-叔丁基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[(3-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-4,7-双(3,5-二-叔丁基苯基)膦基-7“-[(吡啶-2-基甲基)氨基]-2,2”,3,3'-四氢1,1'-螺二茚满 (R)-3-(叔丁基)-4-(2,6-二苯氧基苯基)-2,3-二氢苯并[d][1,3]氧杂磷杂环戊烯 (R)-2-[((二苯基膦基)甲基]吡咯烷 (R)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (N-(4-甲氧基苯基)-N-甲基-3-(1-哌啶基)丙-2-烯酰胺) (5-溴-2-羟基苯基)-4-氯苯甲酮 (5-溴-2-氯苯基)(4-羟基苯基)甲酮 (5-氧代-3-苯基-2,5-二氢-1,2,3,4-oxatriazol-3-鎓) (4S,5R)-4-甲基-5-苯基-1,2,3-氧代噻唑烷-2,2-二氧化物-3-羧酸叔丁酯 (4S,4''S)-2,2''-亚环戊基双[4,5-二氢-4-(苯甲基)恶唑] (4-溴苯基)-[2-氟-4-[6-[甲基(丙-2-烯基)氨基]己氧基]苯基]甲酮 (4-丁氧基苯甲基)三苯基溴化磷 (3aR,8aR)-(-)-4,4,8,8-四(3,5-二甲基苯基)四氢-2,2-二甲基-6-苯基-1,3-二氧戊环[4,5-e]二恶唑磷 (3aR,6aS)-5-氧代六氢环戊基[c]吡咯-2(1H)-羧酸酯 (2Z)-3-[[(4-氯苯基)氨基]-2-氰基丙烯酸乙酯 (2S,3S,5S)-5-(叔丁氧基甲酰氨基)-2-(N-5-噻唑基-甲氧羰基)氨基-1,6-二苯基-3-羟基己烷 (2S,2''S,3S,3''S)-3,3''-二叔丁基-4,4''-双(2,6-二甲氧基苯基)-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2S)-(-)-2-{[[[[3,5-双(氟代甲基)苯基]氨基]硫代甲基]氨基}-N-(二苯基甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[((1S,2S)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[[((1R,2R)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2-硝基苯基)磷酸三酰胺 (2,6-二氯苯基)乙酰氯 (2,3-二甲氧基-5-甲基苯基)硼酸 (1S,2S,3S,5S)-5-叠氮基-3-(苯基甲氧基)-2-[(苯基甲氧基)甲基]环戊醇 (1S,2S,3R,5R)-2-(苄氧基)甲基-6-氧杂双环[3.1.0]己-3-醇 (1-(4-氟苯基)环丙基)甲胺盐酸盐 (1-(3-溴苯基)环丁基)甲胺盐酸盐 (1-(2-氯苯基)环丁基)甲胺盐酸盐 (1-(2-氟苯基)环丙基)甲胺盐酸盐 (1-(2,6-二氟苯基)环丙基)甲胺盐酸盐 (-)-去甲基西布曲明 龙蒿油 龙胆酸钠 龙胆酸叔丁酯 龙胆酸 龙胆紫-d6 龙胆紫