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4(cinnamoyloxy)benzaldehyde | 502618-38-4

中文名称
——
中文别名
——
英文名称
4(cinnamoyloxy)benzaldehyde
英文别名
4-formylphenyl cinnamate;4-formylphenyl (2E)-3-phenylprop-2-enoate;(4-formylphenyl) (E)-3-phenylprop-2-enoate
4(cinnamoyloxy)benzaldehyde化学式
CAS
502618-38-4
化学式
C16H12O3
mdl
——
分子量
252.269
InChiKey
ASHIAZHAFARVET-DHZHZOJOSA-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:
    120 °C
  • 沸点:
    437.3±34.0 °C(Predicted)
  • 密度:
    1.215±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.2
  • 重原子数:
    19
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    43.4
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    4(cinnamoyloxy)benzaldehyde盐酸羟胺sodium acetate 作用下, 以 为溶剂, 反应 4.0h, 以1.2 g的产率得到3-phenylacrylic acid 4-(hydroxyiminomethyl)phenyl ester
    参考文献:
    名称:
    STYRYL CARBOXYLATE DERIVATIVES
    摘要:
    提供了一种新型的苯基羧酸酯衍生物,具有治疗免疫性疾病、炎症、肥胖症、高血脂症、高血压、神经系统疾病和糖尿病的活性。
    公开号:
    US20220234987A1
  • 作为产物:
    描述:
    肉桂酸氯化亚砜三乙胺 作用下, 以 氯仿 为溶剂, 反应 4.0h, 生成 4(cinnamoyloxy)benzaldehyde
    参考文献:
    名称:
    STYRYL CARBOXYLATE DERIVATIVES
    摘要:
    提供了一种新型的苯基羧酸酯衍生物,具有治疗免疫性疾病、炎症、肥胖症、高血脂症、高血压、神经系统疾病和糖尿病的活性。
    公开号:
    US20220234987A1
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文献信息

  • Aminolysis of Y-Substituted Phenyl X-Substituted Cinnamates and Benzoates:  Effect of Modification of the Nonleaving Group from Benzoyl to Cinnamoyl
    作者:Ik-Hwan Um、Youn-Min Park、Mizue Fujio、Masaaki Mishima、Yuho Tsuno
    DOI:10.1021/jo0705061
    日期:2007.6.1
    4-dinitrophenyl X-substituted cinnamates (1a, 1c, and 1e) with amines are curved with a decreasing βnuc value from 0.65 to 0.3−0.4. The reactions of Y-substituted phenyl cinnamates (3a−g) with morpholine also result in a curved Brønsted plot, while the corresponding reactions of Y-substituted phenyl benzoates (4a−e) exhibit a linear Brønsted plot. It has been concluded that the curved Brønsted plots found
    动力学研究报道了Y取代的苯基X取代的肉桂酸酯(1a - e和3a - g)和苯甲酸酯(2a - e和4a - g)与一系列脂环族仲胺在80 mol%H 2 O中的反应/ 20 mol%DMSO在25.0±0.1°C下。2,4-二硝基苯基X-取代的肉桂酸酯(1a - e)和苯甲酸酯(2a - e)与胺的反应产生线性的Yukawa-Tsuno图。的ρ X值是的反应小得多1A - ë比2a - e的要大。的距离效应和反应机理(即,用于协同机制的性质1A - ë)已被建议来负责小ρ X值。2,4-二硝基苯基X-取代的肉桂酸酯(1a,1c和1e)与胺反应的布朗斯台德图是弯曲的,其βnuc值从0.65降低到0.3-0.4。Y取代的苯基肉桂酸酯(3a - g)与吗啉的反应也产生弯曲的布朗斯台德图,而Y取代的苯基苯甲酸酯(4a− e)表现出线性布朗斯台德图。已经得出结论,对于肉桂酸酯(1a,1c,1e和3a
  • Compound, liquid crystal composition, cured substance, optical anisotropic body, and reflection film
    申请人:FUJIFILM Corporation
    公开号:US11193068B2
    公开(公告)日:2021-12-07
    A compound has a strong HTP and a high temperature dependence of HTP. In addition, a liquid crystal composition, a cured substance, an optical anisotropic boy, and a reflection film the above-described compound. The compound is represented by General Formula (1), wherein X1 and X2 each independently represent —CH═CH—or C≡C—.
    化合物具有很强的 HTP 和 HTP 的高温依赖性。此外,一种液晶组合物、一种固化物、一种光学各向异性男孩和一种反射膜就是上述化合物。该化合物由通式(1)表示,其中X1和X2各自独立地代表-CH═CH-或C≡C-。
  • Mesogenic Oxoheterocycles and Their Benzene Analogues
    作者:R. A. Vora、Renu Gupta
    DOI:10.1080/00268948308083073
    日期:1983.1
  • COMPOUND, LIQUID CRYSTAL COMPOSITION, CURED SUBSTANCE, OPTICAL ANISOTROPIC BODY, AND REFLECTION FILM
    申请人:FUJIFILM Corporation
    公开号:US20200071615A1
    公开(公告)日:2020-03-05
    An object of the present invention is to provide a compound having a strong HTP and a high temperature dependence of HTP. In addition, another object is to provide a liquid crystal composition, a cured substance, an optical anisotropic boy, and a reflection film in which the above-described compound is used. The compound of the present invention is represented by General Formula (1).
  • METHOD FOR PRODUCING CHOLESTERIC LIQUID CRYSTAL LAYER, CHOLESTERIC LIQUID CRYSTAL LAYER, LIQUID CRYSTAL COMPOSITION, CURED PRODUCT, OPTICALLY ANISOTROPIC BODY, AND REFLECTIVE LAYER
    申请人:FUJIFILM Corporation
    公开号:US20200409202A1
    公开(公告)日:2020-12-31
    A first object of the present invention is to provide a method for producing a cholesteric liquid crystal layer, which can produce a cholesteric liquid crystal layer whose reflection surface is not parallel to the substrate surface by a simple method. A second object of the present invention is to provide a cholesteric liquid crystal layer, and an optically anisotropic body and a reflective layer, each of which includes the cholesteric liquid crystal layer. A third object of the present invention is to provide a liquid crystal composition capable of forming the cholesteric liquid crystal layer. A fourth object of the present invention is to provide a cured product, an optically anisotropic body, and a reflective layer, each of which is formed of the liquid crystal composition. The method for producing a cholesteric liquid crystal layer of the present invention includes a step 1 of forming a composition layer satisfying the following condition 1, the following condition 2, or the following condition 3 on a substrate, using a liquid crystal composition including a liquid crystal compound; and a step 2 of subjecting the composition layer to a treatment for cholesterically aligning the liquid crystal compound in the composition layer to form a cholesteric liquid crystal layer. Condition 1: at least a part of the liquid crystal compound in the composition layer is tilt-aligned with respect to a substrate surface Condition 2: the liquid crystal compound is aligned such that a tilt angle of the liquid crystal compound in the composition layer continuously changes along a thickness direction; Condition 3: at least a part of the liquid crystal compound in the composition layer is vertically aligned with respect to the substrate surface.
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