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

1-(4-methoxyphenyl)-1-(4-(2-hydroxyethoxy)-phenyl)-2-propyn-1-ol | 1300688-28-1

中文名称
——
中文别名
——
英文名称
1-(4-methoxyphenyl)-1-(4-(2-hydroxyethoxy)-phenyl)-2-propyn-1-ol
英文别名
1-(4-(2-Hydroxyethoxy)phenyl)-1-(4-methoxyphenyl)prop-2-yn-1-ol;1-[4-(2-hydroxyethoxy)phenyl]-1-(4-methoxyphenyl)prop-2-yn-1-ol
1-(4-methoxyphenyl)-1-(4-(2-hydroxyethoxy)-phenyl)-2-propyn-1-ol化学式
CAS
1300688-28-1
化学式
C18H18O4
mdl
——
分子量
298.339
InChiKey
BXLBPNABQBQFJI-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

物化性质

  • 沸点:
    479.6±45.0 °C(Predicted)
  • 密度:
    1.212±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.1
  • 重原子数:
    22
  • 可旋转键数:
    7
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.22
  • 拓扑面积:
    58.9
  • 氢给体数:
    2
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    1-(4-methoxyphenyl)-1-(4-(2-hydroxyethoxy)-phenyl)-2-propyn-1-ol正丁基锂对甲苯磺酸 作用下, 以 四氢呋喃正己烷二氯甲烷 为溶剂, 反应 94.5h, 生成 3-(4-methoxyphenyl)-3-(4-(2-hydroxyethoxy)phenyl)-6-(3-methylmorpholino)-11-fluoro-13,13-dimethyl-3H,13H-indeno[2,1-f]naphtho[1,2-b]pyran
    参考文献:
    名称:
    PHOTOCHROMIC MATERIALS THAT INCLUDE 6-AMINO SUBSTITUTED INDENO-FUSED NAPHTHOPYRANS
    摘要:
    本发明涉及包括某些吲哚并螺[3,3,3]己喹喙的光致变色材料。这些吲哚并螺[3,3,3]己喹喙在6位与氨基团(例如哌啶基或吗啉基)键合,并且在11位可能与卤素基团(例如氟基)键合。本发明的光致变色材料可能具有闭合形式的电磁辐射吸收光谱,其相对于类似的光致变色材料向更长波长(例如大于390纳米的波长)移动。本发明还涉及包括本发明的光致变色材料的光学元件,例如眼镜。
    公开号:
    US20120053341A1
  • 作为产物:
    参考文献:
    名称:
    PHOTOCHROMIC MATERIALS THAT INCLUDE 6-AMINO SUBSTITUTED INDENO-FUSED NAPHTHOPYRANS
    摘要:
    本发明涉及包括某些吲哚并螺[3,3,3]己喹喙的光致变色材料。这些吲哚并螺[3,3,3]己喹喙在6位与氨基团(例如哌啶基或吗啉基)键合,并且在11位可能与卤素基团(例如氟基)键合。本发明的光致变色材料可能具有闭合形式的电磁辐射吸收光谱,其相对于类似的光致变色材料向更长波长(例如大于390纳米的波长)移动。本发明还涉及包括本发明的光致变色材料的光学元件,例如眼镜。
    公开号:
    US20120053341A1
点击查看最新优质反应信息

文献信息

  • CHROMENE COMPOUND, CURABLE COMPOSITION COMPRISING THE COMPOUND, AND OPTICAL ARTICLE INCLUDING A CURED BODY OF THE CURABLE COMPOSITION
    申请人:TOKUYAMA CORPORATION
    公开号:US20200190106A1
    公开(公告)日:2020-06-18
    A chromene compound having at least one indenonaphthopyran moiety which has a group forming a spiro ring together with the 13-position carbon atom and further an oligomer chain group selected from a polyalkylene oxide oligomer chain group having at least three recurring units and a polyester oligomer chain group having at least three recurring units, represented by the following formula and having reduced matrix dependence: wherein R 1 and R 2 are each a group which may have an oligomer chain group, the ring Z bonded to the 13-position carbon atom of the chromene compound is a Spiro ring group, and R 3 and R 4 are each an aryl group or heteroaryl group which may have an oligomer chain group. Preferably, the chromene compound has at least one oligomer chain group in the molecule.
    具有至少一个印苯并萘吡喃基团的色酮化合物,其中该基团与13位碳原子形成螺环,并且进一步具有从至少三个重复单元中选择的聚烷氧基寡聚物链基团和聚酯寡聚物链基团中的一个寡聚物链基团,由下式表示并具有降低的矩阵依赖性: 其中R1和R2是各自可能具有寡聚物链基团的基团,与色酮化合物的13位碳原子键合的环Z是螺环基团,而R3和R4是各自可能具有寡聚物链基团的芳基或杂环基团。最好,该色酮化合物在分子中至少具有一个寡聚物链基团。
  • Photochromic Materials That Include Indeno-Fused Naphthopyrans
    申请人:Bancroft Kevin E.
    公开号:US20120145973A1
    公开(公告)日:2012-06-14
    The present invention relates to photochromic materials that include one or more indeno-fused naphthopyrans that have particular groups at the 7, 11, and 13 positions thereof, and at the position alpha to the oxygen of the pyran ring thereof. With some embodiments, hydrogen or an alkoxy group is bonded to the 7 position, an optionally substituted phenyl is bonded to the 11 position, two alkyl groups are bonded to the 13 position, and two optionally substituted phenyl groups are bonded to the position alpha to the oxygen of the pyran ring of the indeno-fused naphthopyran compound. The 13 position of the indeno-fused naphthopyrans is free of ether groups in which an ether oxygen is bonded to the 13 position, and hydroxyl. The present invention also relates to photochromic articles and compositions that include such indeno-fused naphthopyrans.
    本发明涉及包括一个或多个具有特定基团的吲哚螺合萘并吡喃的光致变色材料,其中该基团位于其7、11和13位置以及其吡喃环氧位的α位置。在某些实施例中,氢或烷氧基与7位置结合,可选取代苯基与11位置结合,两个烷基与13位置结合,并且两个可选取代苯基与吲哚螺合萘并吡喃化合物的吡喃环氧位的α位置结合。吲哚螺合萘并吡喃的13位置不含有醚基,其中醚氧原子与13位置结合,以及羟基。本发明还涉及包括这种吲哚螺合萘并吡喃的光致变色物品和组合物。
  • METHODS FOR PRODUCING PHOTOSENSITIVE MICROPARTICLES
    申请人:Bowles Steven E.
    公开号:US20100221661A1
    公开(公告)日:2010-09-02
    Described are various methods of producing non-aqueous dispersions of photosensitive polymeric microparticles, comprising: (a) preparing one or more aqueous dispersions of a polymerizable component, at least one of which contains a photosensitive material and, wherein the polymerizable components comprise at least one hydrophilic functional group and/or at least one hydrophobic functional group; (b) subjecting the dispersion of (a) to conditions sufficient to form microparticles; (c) at least partially polymerizing the polymerizable component; (d) combining the dispersion with an organic continuous phase comprising an organic solvent; (e) removing water from the dispersion such that the final water content of the non-aqueous dispersion is less than 30 percent by weight; wherein e) is performed before or after d); and (f) reacting any acid functional groups on the surface of the microparticles with a reactive material having at least one epoxy functional group, at least one thiocarbonylthio functional group, at least one alkoxyamine functional group, or at least one halide functional group.
    本文描述了制备非水分散的光敏聚合微粒的各种方法,包括:(a)制备一种或多种聚合组分的水分散液,其中至少一种含有光敏材料,所述聚合组分包括至少一种亲水性功能基和/或至少一种疏水性功能基;(b)将(a)的分散液置于足以形成微粒的条件下;(c)至少部分聚合聚合组分;(d)将分散液与包含有机溶剂的有机连续相结合;(e)去除分散液中的水分,使得最终的非水分散液的水含量小于30重量%;其中e)在d)之前或之后执行;(f)用至少一种环氧功能基、至少一种硫代氨基酸功能基、至少一种烷氧胺功能基或至少一种卤素功能基的反应性材料反应微粒表面上的任何酸性功能基。
  • PHOTOCHROMIC MATERIALS
    申请人:Tomasulo Massimiliano
    公开号:US20110108781A1
    公开(公告)日:2011-05-12
    The present invention relates to photochromic materials that include a photochromic compound that includes a photochromic substituent (e.g., an indeno-fused naphthopyran) and at least one pendent silane group, which is bonded to the photochromic substituent. The pendent silane groups are selected from certain pendent siloxy-silane groups and/or pendent alkoxy-silane groups represented by general formulas (I) and/or (II) as described in further detail herein. The present invention also relates to photochromic articles, such as photochromic optical elements (e.g., photochromic lenses), and photochromic coating compositions (e.g., curable photochromic coating compositions), that include the photochromic materials of the present invention. The photochromic materials of the present invention have improved compatibility with compositions into which they may be incorporated, for example, coating compositions, such as urethane coating compositions.
    本发明涉及包括具有光致变色取代基(例如,吲哚并环戊基吡喃)和至少一个侧基硅烷基的光致变色化合物的光致变色材料。侧基硅烷基从描述的通用式(I)和/或(II)表示的某些侧基硅氧烷基和/或侧基烷氧基中选择。本发明还涉及光致变色物品,例如光致变色光学元件(例如,光致变色透镜)和光致变色涂层组合物(例如,可固化的光致变色涂层组合物),其中包括本发明的光致变色材料。本发明的光致变色材料与可能加入其中的组合物(例如,涂层组合物,例如脲基涂层组合物)具有改进的相容性。
  • Photochromic Compounds Having At Least Two Photochromic Moieties
    申请人:Lu Yunyi
    公开号:US20120136148A1
    公开(公告)日:2012-05-31
    The present invention relates to photochromic compounds that include at least two photochromic moieties that are linked together by a multivalent linking group. The multivalent linking group can be selected so as to be flexible and/or substantially prevent electronic interaction between any two photochromic moieties through the multivalent linking group. The present invention also relates to photochromic compositions and articles that include at least a photochromic amount of one or more photochromic compounds of the present invention.
    本发明涉及包含至少两个光致变色基团的光致变色化合物,这些基团通过多价连接基团连接在一起。多价连接基团可以选择为柔性的和/或通过多价连接基团在任何两个光致变色基团之间实现电子相互作用的阻止。本发明还涉及包括本发明中至少一种光致变色化合物的光致变色组合物和物品。
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)-(-)-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)-(+)-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)-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 (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 (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 (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-[[[[[[((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 (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 (-)-去甲基西布曲明 龙胆酸钠 龙胆酸叔丁酯 龙胆酸 龙胆紫 龙胆紫 齐达帕胺 齐诺康唑 齐洛呋胺 齐墩果-12-烯[2,3-c][1,2,5]恶二唑-28-酸苯甲酯 齐培丙醇 齐咪苯 齐仑太尔 黑染料 黄酮,5-氨基-6-羟基-(5CI) 黄酮,6-氨基-3-羟基-(6CI) 黄蜡,合成物 黄草灵钾盐