(1-(3-(4-methoxyphenyl)acryloyl)imidazole)

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 肉桂酸及其衍生物
• 英文名称: (1-(3-(4-methoxyphenyl)acryloyl)imidazole)
• 英文别名: 1-Imidazol-1-yl-3-(4-methoxyphenyl)prop-2-en-1-one；1-imidazol-1-yl-3-(4-methoxyphenyl)prop-2-en-1-one
• 化学式: C₁₃H₁₂N₂O₂
• 分子量: 228.25
• InChiKey: UQGJAZKPYKZBSG-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2
• 重原子数：
  17
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.08
• 拓扑面积：
  44.1
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  (1-(3-(4-methoxyphenyl)acryloyl)imidazole) 在 咪唑 、 水 作用下， 反应 336.0h， 生成 3-imidazolyl-3-(4-methoxyphenyl)propionic acid
  参考文献：
  名称：

  IMIDAZOLE COMPOUND, METAL SURFACE TREATMENT LIQUID, METAL SURFACE TREATMENT METHOD, AND LAMINATE PRODUCTION METHOD

  摘要：

  一种新型咪唑化合物，可产生一种表面处理液，该液非常有效地抑制导线表面的迁移和氧化；一种含有咪唑化合物的金属表面处理液；一种使用金属表面处理液的金属表面处理方法；以及一种使用表面处理液的层压板生产方法。使用包含饱和脂肪酸或饱和脂肪酸酯的表面处理液对金属进行表面处理，其中，预定位置被预定结构的芳基取代，并且可能带有取代基的咪唑基。

  公开号：

  US20170247334A1
• 作为产物：
  描述：

  咪唑 、 p-methoxycinnamoyl chloride 在 三乙胺 作用下， 以 乙酸乙酯 为溶剂， 反应 1.0h， 以2.5 kg的产率得到(1-(3-(4-methoxyphenyl)acryloyl)imidazole)
  参考文献：
  名称：

  CRYSTALS CONTAINING UNSATURATED CARBOXYLIC ACID AMIDE COMPOUND AND METHOD FOR PRODUCING SAME

  摘要：

  提供的是一种不饱和羧酸酰胺的晶体。该晶体可用作或用于精细化学品，如制药、农药、聚合材料、功能材料以及它们的中间体，具有高纯度，仍然不臃肿，并且可以得到出色处理。该晶体包括95%或更多面积的由式（1）表示的不饱和羧酸酰胺，并且具有0.2至0.7克/毫升的堆积密度。在该式中，R1到R5独立选择自氢、烷基、羟基、烷氧基和硝基。R1到R5中至少两个可以连接在一起形成一个环，与构成指定芳香环的碳原子一起。R6、R7和R8独立选择自氢、烷基和芳基。R7和R8可以连接在一起形成一个环，与构成指定咪唑环的碳原子一起。

  公开号：

  US20150158820A1

文献信息

• CRYSTALS CONTAINING UNSATURATED CARBOXYLIC ACID AMIDE COMPOUND AND METHOD FOR PRODUCING SAME
  申请人：DAICEL CORPORATION

  公开号：US20150158820A1

  公开（公告）日：2015-06-11

  Provided is a crystal of an unsaturated carboxylic acid amide. The crystal is useful as or for fine chemicals such as pharmaceuticals, agricultural chemicals, polymeric materials, functional materials, and intermediates of them, has a high purity, still is not bulky, and can be handled excellently. The crystal includes an unsaturated carboxylic acid amide represented by Formula (1) in an amount of 95 percent by area or more and has a bulk density of 0.2 to 0.7 g/mL. In the formula, R 1 to R 5 are independently selected from hydrogen, alkyl, hydroxyl, alkoxy, and nitro. At least two of R 1 to R 5 may be linked to form a ring together with carbon atoms constituting the specified aromatic ring. R 6 , R 7 , and R 8 are independently selected from hydrogen, alkyl, and aryl. R 7 and R 8 may be linked to form a ring together with carbon atoms constituting the specified imidazole ring.

  提供的是一种不饱和羧酸酰胺的晶体。该晶体可用作或用于精细化学品，如制药、农药、聚合材料、功能材料以及它们的中间体，具有高纯度，仍然不臃肿，并且可以得到出色处理。该晶体包括95%或更多面积的由式（1）表示的不饱和羧酸酰胺，并且具有0.2至0.7克/毫升的堆积密度。在该式中，R1到R5独立选择自氢、烷基、羟基、烷氧基和硝基。R1到R5中至少两个可以连接在一起形成一个环，与构成指定芳香环的碳原子一起。R6、R7和R8独立选择自氢、烷基和芳基。R7和R8可以连接在一起形成一个环，与构成指定咪唑环的碳原子一起。
• Acyclic 1,2-/1,3-mixed pentols. Synthesis and general trends in bichromophoric exciton coupled circular dichroic spectra
  作者：Dinesh Rele、Ning Zhao、Nakanishi Koji、Berova Nina

  DOI：10.1016/0040-4020(96)00012-9

  日期：1996.2

  The synthesis of all eight configurational isomers of acyclic 1,2,3,4,6-pentols belonging to the 2R enantiomeric series is described. The 1-anthroyl-2,3,4,6-p-methoxycinnamates of these pentols give rise to unique exciton coupled circular dichroic spectra in the range of 220–380 nm. Comparisons with the CD of corresponding bichromophoric derivatives of the lower homologous tetrols, 1-anthroyl-2,3,

  描述了属于2 R对映体系列的无环1,2,3,4,6-戊醇的所有八个构型异构体的合成。这些戊醇的1-蒽基-2,3,4,6-对甲氧基肉桂酸酯在220–380 nm范围内产生独特的激子耦合圆二色光谱。与较低同源四元酚1-蒽基-2,3,4-对甲氧基肉桂酸酯的相应双色衍生物的CD的比较导致可预测的总体趋势，其中仅少量差异源自1,3- syn延伸，而主要差异产生从1,3-反扩展。
• IMIDAZOLE COMPOUND, METAL SURFACE TREATMENT LIQUID, METAL SURFACE TREATMENT METHOD, AND LAMINATE PRODUCTION METHOD
  申请人：TOKYO OHKA KOGYO CO., LTD.

  公开号：US20170247334A1

  公开（公告）日：2017-08-31

  A novel imidazole compound that yields a surface treatment liquid that is very effective at suppressing migration and oxidation of a wiring surface; a metal surface treatment liquid that contains the imidazole compound; a metal surface treatment method that uses the metal surface treatment liquid; and a laminate production method that uses the surface treatment liquid. A metal is surface-treated using the surface treatment liquid which includes a saturated fatty acid or a saturated fatty acid ester of a specific structure, in which a prescribed position is substituted by an aromatic group of a prescribed structure and an imidazolyl group that may have a substituent group.

  一种新型咪唑化合物，可产生一种表面处理液，该液非常有效地抑制导线表面的迁移和氧化；一种含有咪唑化合物的金属表面处理液；一种使用金属表面处理液的金属表面处理方法；以及一种使用表面处理液的层压板生产方法。使用包含饱和脂肪酸或饱和脂肪酸酯的表面处理液对金属进行表面处理，其中，预定位置被预定结构的芳基取代，并且可能带有取代基的咪唑基。
• NOVEL BASE GENERATOR AND ADHESION ENHANCER
  申请人：Tokyo Ohka Kogyo Co., Ltd.

  公开号：EP2725011B1

  公开（公告）日：2021-10-27
• 안료 분산액 및 그것을 사용한 감광성 수지 조성물의 제조 방법
  申请人：TOKYO OHKA KOGYO CO., LTD. 도쿄 오카 고교 가부시키가이샤(519980627398)

  公开号：KR102140676B1

  公开（公告）日：2020-08-04

  [과제]시간 경과 후의 안료의 분산성이 양호하고, 저노광량으로 고밀착성인 미소 패턴을 형성 가능한 감광성 수지 조성물을 시간 경과 후에도 부여할 수 있는 안료 분산액 및 그것을 사용한 감광성 수지 조성물의 제조 방법을 제공한다. [해결 수단]본 발명과 관련된 안료 분산액은 안료와, 용제와, 하기 식(1)로 나타내는 화합물을 함유한다. 식 중, R1 및 R2는 각각 독립적으로 수소 원자 또는 유기기를 나타내지만, 적어도 한쪽은 유기기를 나타낸다. R1 및 R2는 이들이 결합해 환상 구조를 형성하고 있어도 되고, 헤테로 원자의 결합을 포함하고 있어도 된다. R3은 단결합 또는 유기기를 나타낸다. R4~R9는 각각 독립적으로 수소 원자, 유기기 등을 나타내지만, R6 및 R7이 수산기가 되는 경우는 없다. R10은 수소 원자 또는 유기기를 나타낸다.

  The dispersibility of the pigment after a period of time is good, and a photosensitive resin composition capable of forming fine patterns with low exposure doses and high resolution can be provided with a pigment dispersion liquid that can be applied even after a period of time, and a method for manufacturing a photosensitive resin composition using the pigment dispersion liquid. The pigment dispersion liquid related to the present invention contains a pigment, a solvent, and a compound represented by formula (1). In the formula, R1 and R2 independently represent a hydrogen atom or an organic group, but at least one of them represents an organic group. R1 and R2 may form a cyclic structure by bonding, and may include a bond of a hetero atom. R3 represents a single bond or an organic group. R4 to R9 independently represent a hydrogen atom, an organic group, etc., but R6 and R7 do not become hydroxy groups. R10 represents a hydrogen atom or an organic group.