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-phenyl-2-methoxycarbonyl-4-acetoxy-naphthalene | 99303-73-8

中文名称
——
中文别名
——
英文名称
1-phenyl-2-methoxycarbonyl-4-acetoxy-naphthalene
英文别名
methyl ester of 4-acetoxy-1-phenyl-2-naphthoic acid;Methyl4-acetoxy-1-phenyl-2-naphthoate;methyl 4-acetyloxy-1-phenylnaphthalene-2-carboxylate
1-phenyl-2-methoxycarbonyl-4-acetoxy-naphthalene化学式
CAS
99303-73-8
化学式
C20H16O4
mdl
——
分子量
320.345
InChiKey
LODJLIXTQXVWGZ-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

  • 熔点:
    96-98 °C(Solv: methanol (67-56-1); water (7732-18-5))
  • 沸点:
    484.3±45.0 °C(Predicted)
  • 密度:
    1.211±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.4
  • 重原子数:
    24
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.1
  • 拓扑面积:
    52.6
  • 氢给体数:
    0
  • 氢受体数:
    4

上下游信息

  • 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:
    参考文献:
    名称:
    [EN] METHOD FOR PREPARING INDOLENAPHTHOPYRANS
    [FR] PROCÉDÉ DE PRÉPARATION D'INDOLENAPHTOPYRANES
    摘要:
    提供了一种合成中间体,用于制备具有式(I)核心骨架结构的光致变色吲哚萘吡喃化合物,其中m为0至4,n为0至4,R1和R2分别独立为羟基、氰基、(甲基)丙烯酸酯、氨基、卤素、取代或未取代的烷基、硼酯、硼酸、聚醚、聚酯、聚碳酸酯、聚氨酯、取代或未取代的芳基、取代或未取代的杂环芳基、取代或未取代的杂芳基、取代或未取代的烷氧基、取代或未取代的芳氧基、取代或未取代的烷硫基、取代或未取代的芳硫基、酮、醛、酯、羧酸、羧酸酯、酰胺、碳酸酯、氨基甲酸酯、脲、硅氧烷、烷氧基硅烷或聚硅氧烷;R3为取代或未取代的2-吡啶基或取代或未取代的2-喹啉基;R4为氢、取代或未取代的烷基、烷氧甲基、取代或未取代的硅基或酰基。还提供了一种制备吲哚萘酚化合物的方法,包括在催化剂存在下使式(I)的苯基萘酚化合物环化。
    公开号:
    WO2020126033A1
  • 作为产物:
    描述:
    乙酸酐3-Carbomethoxy-4,4-diphenyl-3-butenoic acid甲苯 为溶剂, 反应 16.0h, 以88%的产率得到1-phenyl-2-methoxycarbonyl-4-acetoxy-naphthalene
    参考文献:
    名称:
    [EN] METHOD FOR PREPARING INDOLENAPHTHOPYRANS
    [FR] PROCÉDÉ DE PRÉPARATION D'INDOLENAPHTOPYRANES
    摘要:
    提供了一种合成中间体,用于制备具有式(I)核心骨架结构的光致变色吲哚萘吡喃化合物,其中m为0至4,n为0至4,R1和R2分别独立为羟基、氰基、(甲基)丙烯酸酯、氨基、卤素、取代或未取代的烷基、硼酯、硼酸、聚醚、聚酯、聚碳酸酯、聚氨酯、取代或未取代的芳基、取代或未取代的杂环芳基、取代或未取代的杂芳基、取代或未取代的烷氧基、取代或未取代的芳氧基、取代或未取代的烷硫基、取代或未取代的芳硫基、酮、醛、酯、羧酸、羧酸酯、酰胺、碳酸酯、氨基甲酸酯、脲、硅氧烷、烷氧基硅烷或聚硅氧烷;R3为取代或未取代的2-吡啶基或取代或未取代的2-喹啉基;R4为氢、取代或未取代的烷基、烷氧甲基、取代或未取代的硅基或酰基。还提供了一种制备吲哚萘酚化合物的方法,包括在催化剂存在下使式(I)的苯基萘酚化合物环化。
    公开号:
    WO2020126033A1
点击查看最新优质反应信息

文献信息

  • NOVEL PHENYLNAPHTHOL DERIVATIVES
    申请人:TOKUYAMA CORPORATION
    公开号:US20160130203A1
    公开(公告)日:2016-05-12
    Phenylnaphthol derivatives represented by the following general formula (1), wherein, R 1 to R 3 are hydrogen atoms, alkyl groups or aryl groups, and R 2 and R 3 may be bonded together to form an aliphatic hydrocarbon ring or a heterocyclic ring, a and b are, respectively, integers of 0 to 4, R 4 and R 5 are hydroxyl groups, alkyl groups, haloalkyl groups, cycloalkyl groups, alkoxy groups, amino groups, heterocyclic groups having a nitrogen atom as a hetero atom and are bonded together via the nitrogen atom, cyano groups, nitro groups, formyl groups, hydroxycarbonyl groups, alkylcarbonyl groups, alkoxycarbonyl groups, halogen atoms, aralkyl groups, aralkoxy groups, aryloxy groups, aryl groups, heteroaryl groups bonded together via a carbon atom in the ring, alkylthio groups, cycloalkylthio groups, arylthio groups or heteroarylthio groups, and if R 4 or R 5 are present in a plural number, the plurality of R 4 or the plurality of R 5 may be the same or different, or 2 R 4 s or 2 R 5 s may be bonded together to form an alicyclic hydrocarbon ring or a heterocyclic ring. The compounds are useful as intermediate products for the synthesis of, for example, photochromic compounds.
    以下是由下列一般式(1)表示的苯基萘酚衍生物, 其中,R1至R3为氢原子、烷基或芳基,R2和R3可以结合在一起形成脂肪烃环或杂环,a和b分别为0至4的整数,R4和R5为羟基、烷基、卤代烷基、环烷基、烷氧基、氨基、含氮原子作为杂原子的杂环基,并通过氮原子结合在一起,氰基、硝基、甲酰基、羟基羰基基、烷基羰基基、烷氧羰基基、卤素原子、芳基烷基、芳基氧基、芳基氧基、芳基、通过环中的碳原子结合在一起的杂芳基、烷硫基、环烷硫基、芳硫基或杂芳硫基,如果R4或R5以复数形式存在,则复数的R4或复数的R5可以相同或不同,或2个R4或2个R5可以结合在一起形成脂环烃环或杂环。这些化合物可用作合成光变化化合物的中间产物。
  • [EN] METHOD FOR PREPARING INDOLENAPHTHOPYRANS<br/>[FR] PROCÉDÉ DE PRÉPARATION D'INDOLENAPHTOPYRANES
    申请人:TRANSITIONS OPTICAL LTD
    公开号:WO2020126033A1
    公开(公告)日:2020-06-25
    Provided is a synthetic intermediate for the preparation of photochromic indolenaphthopyran compounds having the core skeletal structure of Formula (I): wherein m is 0 to 4, n is 0 to 4, R1 and R2 are each independently hydroxyl, cyano, (meth)acrylate, amino, halo, substituted or unsubstituted alkyl, boronic ester, boronic acid, polyether, polyester, polycarbonate, polyurethane, substituted or unsubstituted aryl, substituted or unsubstituted heterocycloaryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted alkoxy, substituted or unsubstituted aryloxy, substituted or unsubstituted alkylthio, substituted or unsubstituted arylthio, ketone, aldehyde, ester, carboxylic acid, carboxylate, amide, carbonate, carbamate, urea, siloxane, alkoxysilane, or polysiloxane; R3 is substituted or unsubstituted 2-pyridyl or substituted or unsubstituted 2-quinolyl; and R4 is hydrogen, substituted or unsubstituted alkyl, alkoxymethyl, substituted or unsubstituted silyl, or acyl. Also provided is a process for producing an indolenaphthol compound which includes cyclizing the phenylnaphthol compound of Formula (I) in the presence of a catalyst.
    提供了一种合成中间体,用于制备具有式(I)核心骨架结构的光致变色吲哚萘吡喃化合物,其中m为0至4,n为0至4,R1和R2分别独立为羟基、氰基、(甲基)丙烯酸酯、氨基、卤素、取代或未取代的烷基、硼酯、硼酸、聚醚、聚酯、聚碳酸酯、聚氨酯、取代或未取代的芳基、取代或未取代的杂环芳基、取代或未取代的杂芳基、取代或未取代的烷氧基、取代或未取代的芳氧基、取代或未取代的烷硫基、取代或未取代的芳硫基、酮、醛、酯、羧酸、羧酸酯、酰胺、碳酸酯、氨基甲酸酯、脲、硅氧烷、烷氧基硅烷或聚硅氧烷;R3为取代或未取代的2-吡啶基或取代或未取代的2-喹啉基;R4为氢、取代或未取代的烷基、烷氧甲基、取代或未取代的硅基或酰基。还提供了一种制备吲哚萘酚化合物的方法,包括在催化剂存在下使式(I)的苯基萘酚化合物环化。
  • Photochromic materials having extended pi-conjugated systems and compositions and articles including the same
    申请人:Kim Beon-Kyu
    公开号:US20060228557A1
    公开(公告)日:2006-10-12
    Various non-limiting embodiments disclosed herein relate to photochromic materials having extended pi-conjugated systems. For example, various non-limiting embodiments disclosed herein provide a photochromic material, such as an indeno-fused naphthopyran, which comprises a group that extends the pi-conjugated system of the indeno-fused naphthopyran bonded at the 11-position thereof. Further, the photochromic materials according to certain non-limiting embodiments disclosed herein may display hyperchromic absorption of electromagnetic radiation as compared to conventional photochromic materials and/or may have a closed-form absorption spectrum that is bathochromically shifted as compared to conventional photochromic materials. Other non-limiting embodiments relate to photochromic compositions and photochromic articles, such as optical elements, made using the disclosed photochromic materials, and methods of making the same.
    本文披露的各种非限制性实施例涉及具有扩展π共轭系统的光致变色材料。例如,本文披露的各种非限制性实施例提供了一种光致变色材料,例如吲哚并螺并萘哌啶,其包括延伸吲哚并螺并萘哌啶的π共轭系统的基团,该基团与其11位键合。此外,根据本文披露的某些非限制性实施例,与传统光致变色材料相比,光致变色材料可能显示出电磁辐射的高吸光度,和/或具有相对于传统光致变色材料的向红移的闭合吸收光谱。其他非限制性实施例涉及使用所披露的光致变色材料制造的光致变色组合物和光致变色物品,例如光学元件,以及制造这些物品的方法。
  • Photochromic indeno-fused naphthopyrans
    申请人:Chopra Anu
    公开号:US20070138448A1
    公开(公告)日:2007-06-21
    Photochromic materials comprising indeno-fused naphthopyrans having substituents comprising a 4-fluorophenyl group and a 4-aminophenyl group bonded to the 3-position of the indeno-fused naphthopyran are disclosed. The photochromic materials may exhibit faster fade rates as compared to similar indeno-fused naphthopyrans without a 4-fluorophenyl group and a 4-aminophenyl group bonded to the 3-position of the indeno-fused naphthopyran. Substituted 2-propyn-1-ols utilized for the synthesis of the indeno-fused naphthopyrans disclosed herein are disclosed. Photochromic compositions and articles, such as optical elements, incorporating the photochromic materials disclosed herein are also disclosed.
    本文披露了一种包含取代基的吲哚并萘噻吩的光致变色材料,该取代基包括与吲哚并萘噻吩的3位键合的4-氟苯基和4-氨基苯基。与没有4-氟苯基和4-氨基苯基键合到吲哚并萘噻吩的类似吲哚并萘噻吩相比,光致变色材料可能表现出更快的褪色速率。本文还披露了用于合成本文所披露的吲哚并萘噻吩的取代2-丙炔-1-醇。本文还披露了包含本文所披露的光致变色材料的光致变色组合物和物品,例如光学元件。
  • Photochromic materials
    申请人:Wang Feng
    公开号:US20060022176A1
    公开(公告)日:2006-02-02
    Various non-limiting embodiments disclosed herein related to photochromic materials comprising the reaction product of (a) at least one ring-opening cyclic monomer, and (b) a photochromic initiator. Other non-limiting embodiments related to photochromic materials represented by: wherein S′ comprises the at least one ring-opened cyclic monomer as set forth herein. Other non-limiting embodiments related to photochromic compositions, optical elements, and methods of inhibiting migration of a photochromic material in a polymeric material using the photochromic materials disclosed herein. Methods of making such photochromic materials, compositions, and optical elements are also disclosed.
    本文披露了各种非限制性实施例,涉及光致变色材料,其包括(a)至少一种开环环状单体的反应产物,以及(b)光致变色引发剂。其他非限制性实施例涉及光致变色材料,该材料由下式表示:其中S’包括如本文所述的至少一种开环环状单体。其他非限制性实施例涉及光致变色组合物、光学元件和使用本文所披露的光致变色材料抑制聚合物材料中光致变色材料迁移的方法。本文还披露了制备此类光致变色材料、组合物和光学元件的方法。
查看更多