(2-formyl-4-methoxyphenoxy)acetic acid | 24589-93-3

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: (2-formyl-4-methoxyphenoxy)acetic acid
• 英文别名: 2-(2-formyl-4-methoxyphenoxy)acetic acid；4-Methoxy-2-formyl-phenoxyessigsaeure；(2-Formyl-4-methoxy-phenoxy)-essigsaeure
• CAS: 24589-93-3
• 化学式: C₁₀H₁₀O₅
• mdl: MFCD09673329
• 分子量: 210.186
• InChiKey: BTPORJVAKLIAGD-UHFFFAOYSA-N

物化性质

• 熔点：
  155-156 °C
• 沸点：
  414.1±30.0 °C(Predicted)
• 密度：
  1.311±0.06 g/cm3(Predicted)
• 溶解度：
  可溶于氯仿（轻微、加热、超声处理）、DMSO（轻微）、甲醇（轻微）

计算性质

• 辛醇/水分配系数(LogP)：
  1
• 重原子数：
  15
• 可旋转键数：
  5
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.2
• 拓扑面积：
  72.8
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  (2-formyl-4-methoxyphenoxy)acetic acid 在 三乙烯二胺 、 三甲基乙酰氯 、 N,N-二异丙基乙胺 作用下， 以 乙醇 、 二氯甲烷 为溶剂， 反应 3.5h， 生成 10-methoxy-2-phenyl-11bH-benzo[f][1,3,4]oxadiazolo[3,2-d][1,4]oxazepin-5(6H)-one
  参考文献：
  名称：

  Organocatalytic Synthesis of Fused Bicyclic 2,3-Dihydro-1,3,4-oxadiazoles through an Intramolecular Cascade Cyclization

  摘要：

  Hydrazone-carboxylic acids undergo intramolecular cyclization in the presence of pivaloyl chloride, iPr(2)NEt, and catalytic DABCO to form a range of substituted fused tricyclic 2,3-dihydro-1,3,4-oxadiazoles in high yields.

  DOI：

  10.1021/acs.orglett.5b02997
• 作为产物：
  描述：

  tert-butyl 2-(2-formyl-4-methoxyphenoxy)acetate 在 三氟乙酸 作用下， 以 二氯甲烷 为溶剂， 反应 3.0h， 以86%的产率得到(2-formyl-4-methoxyphenoxy)acetic acid
  参考文献：
  名称：

  Organocatalytic Synthesis of Fused Bicyclic 2,3-Dihydro-1,3,4-oxadiazoles through an Intramolecular Cascade Cyclization

  摘要：

  Hydrazone-carboxylic acids undergo intramolecular cyclization in the presence of pivaloyl chloride, iPr(2)NEt, and catalytic DABCO to form a range of substituted fused tricyclic 2,3-dihydro-1,3,4-oxadiazoles in high yields.

  DOI：

  10.1021/acs.orglett.5b02997

文献信息

• N-(4- carbamimidoyl-phenyl) -glycine derivatives
  申请人：——

  公开号：US20010001799A1

  公开（公告）日：2001-05-24

  The invention is concerned with novel N-(4-carbamimidoyl-phenyl)-glycine derivatives of the formula: 1 wherein R 1 , E, X 1 to X 4 and G 1 and G 2 are as defined in the description and the claims, as well as hydrates or solvates and physiologically usable salts thereof.

  这项发明涉及一种新颖的公式为N-(4-羰基苄基)-甘氨酸衍生物，其中R1、E、X1至X4以及G1和G2如描述和权利要求中所定义，以及其水合物或溶剂合物和生理可用盐。
• N- (4-carbamimidoyl-phenyl) -glycine derivatives
  申请人：——

  公开号：US20030083504A1

  公开（公告）日：2003-05-01

  The invention is concerned with novel N-(4-carbamimidoyl-phenyl)-glycine derivatives of the formula: 1 wherein R 1 , E, X 1 to X 4 and G 1 and G 2 are as defined in the description and the claims, as well as hydrates or solvates and physiologically usable salts thereof.

  本发明涉及一种新的N-(4-氨基甲酰基苯基)-甘氨酸衍生物，其化学式为：1，其中R1、E、X1至X4和G1和G2如说明书和权利要求所定义，以及其水合物或溶剂化合物和生理上可用的盐。
• 699. Organic fluoro-compounds. Part VII. Some 2-trihalogenocoumarones
  作者：W. B. Whalley

  DOI：10.1039/jr9530003479

  日期：——
• Synthesis and aldose reductase inhibitory activity of a new series of 5-[[2-(ω-carboxyalkoxy)aryl]methylene]-4-oxo-2-thioxothiazolidine derivatives
  作者：Makoto Murata、Buichi Fujitani、Hiroyuki Mizuta

  DOI：10.1016/s0223-5234(99)00128-2

  日期：1999.12

  A new series of 5-[[2-(omega-carboxyalkoxy)aryl]methylene]-4-oxo-2-thioxothiazolidine derivatives was synthesized and evaluated for their potency as aldose reductase inhibitors (ARIs). Their activities were examined in terms of their inhibitory effect on rat lens aldose reductase in vitro and in terms of the preventive effect on sorbitol accumulation in the sciatic nerve of streptozotocin (STZ)-induced diabetic rats in vivo. Of these compounds, some of the naphthylmethylene thiazolidine derivatives were comparable to Zenarestat in the inhibitory potency in vitro and in vivo. In particular, compound 30 was 1.5 times more potent than Zenarestat in the in vivo activity, and had an adequate potency for clinical development. (C) 1999 Editions scientifiques et medicales Elsevier SAS.
• Pyridoxal phosphate. II. Benzene analogs. 2-Formylphenoxyacetic acids as potential antimetabolites of pyridoxal phosphate
  作者：Theodore L. Hullar、D. L. Failla

  DOI：10.1021/jm00303a018

  日期：1969.5