benzo[d][1,3]dioxol-5-yl propionate | 112579-46-1

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并间二氧杂环戊烯类
• 英文名称: benzo[d][1,3]dioxol-5-yl propionate
• 英文别名: 5-propionyloxy-benzo[1,3]dioxole；5-Propionyloxy-benzo[1,3]dioxol；methyl 3,4-methylenedioxyphenyl acetate；sesamyl propanoate；1,3-Benzodioxol-5-yl propanoate
• CAS: 112579-46-1
• 化学式: C₁₀H₁₀O₄
• 分子量: 194.187
• InChiKey: BDDLDIIUBNOJJT-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.8
• 重原子数：
  14
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  44.8
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  benzo[d][1,3]dioxol-5-yl propionate 在 sodium hydroxide 、 四丁基氯化铵 、 水 、 盐酸 作用下， 以 二氯甲烷 、 水 为溶剂， 反应 8.75h， 以92.3%的产率得到芝麻酚
  参考文献：
  名称：

  [EN] PROCESS FOR PREPARING ALKOXY- AND ARYLOXY-PHENOLS
  [FR] PROCEDE DE PREPARATION D'ALCOXY- ET D'ARYLOXY-PHENOLS

  摘要：

  公开号：

  WO2004092106A3
• 作为产物：
  描述：

  3,4-(亚甲基二氧)苯丙酮 在 甲酸 、 双氧水 作用下， 以 二氯甲烷 、 水 为溶剂， 反应 12.0h， 以94.5%的产率得到benzo[d][1,3]dioxol-5-yl propionate
  参考文献：
  名称：

  [EN] PROCESS FOR PREPARING ALKOXY- AND ARYLOXY-PHENOLS
  [FR] PROCEDE DE PREPARATION D'ALCOXY- ET D'ARYLOXY-PHENOLS

  摘要：

  公开号：

  WO2004092106A3

文献信息

• Palladium-Catalyzed Direct Dicarbonylation of Amines with Ethylene to Imides
  作者：Chang-Sheng Kuai、Le-Cheng Wang、Jian-Xing Xu、Xiao-Feng Wu

  DOI：10.1021/acs.orglett.1c04142

  日期：2022.1.14

  value-added products through catalytic strategy has a wide range of practical significance. Here, a palladium-catalyzed method for the direct and efficient dicarbonylation of amines with basic industrial feedstock ethylene to imide has been developed. Moderate to excellent yields of the desired imides can be produced from readily available amines in a straightforward manner.

  通过催化策略将低成本、简单的大宗化学品选择性有效地转化为高附加值产品具有广泛的现实意义。在这里，已经开发了一种钯催化的方法，用于将胺与基本工业原料乙烯直接有效地二羰基化为酰亚胺。可以从容易获得的胺以简单的方式生产中等至优异产率的所需酰亚胺。
• SUBSTITUTED CATHECHOLS AS INHIBITORS OF IL-4 AND IL-5 FOR THE TREATMENT BRONCHIAL ASTHMA
  申请人：Bandyopadhyay Santu

  公开号：US20140135393A1

  公开（公告）日：2014-05-15

  The present invention relates to compounds of general formula 1 for the treatment of bronchial asthma by inhibition of IL-4 or IL-5 pathway inhibition. The present invention also relates to the use of compound of general formula 1 for the treatment of bronchial by inhibition of IL-4 or IL-5 pathway. The present invention also relates to the method of treating asthma by inhibition of IL-4 or IL-5 pathway by administration of compound or said composition through oral, intranasal, route or by inhalation to a mammal in need thereof. Compound of general formula 1 may be used for reducing perivascular and peribronchial inflammation.

  本发明涉及通式1的化合物，用于通过抑制IL-4或IL-5途径的抑制治疗支气管哮喘。本发明还涉及使用通式1的化合物通过抑制IL-4或IL-5途径的抑制治疗支气管哮喘。本发明还涉及通过口服、鼻内、或吸入途径向需要治疗的哺乳动物给予化合物或所述组合物来抑制IL-4或IL-5途径以治疗哮喘的方法。通式1的化合物可用于减少周围血管和支气管炎症。
• [EN] INHIBITORS OF PHOSPHATIDYLINOSITOL-3-KINASE (PI3) AND INDUCERS OF NITRIC OXIDE (NO)<br/>[FR] INHIBITEURS DE LA PHOSPHATIDYLINOSITOL-3-KINASE (PI3) ET INDUCTEURS D'OXYDE NITRIQUE (NO)
  申请人：COUNCIL SCIENT IND RES

  公开号：WO2010079423A1

  公开（公告）日：2010-07-15

  The present invention relates to compounds of general formula 1 for the treatment of malignancy by inhibition of PI3-Akt pathway and or induction of NO. The present invention also relates to the use of compound of general formula 1 for the treatment of malignancy by inhibition of PI3-Akt pathway and or induction of NO. The present invention further relates to a method of treating malignancy by inhibition of PI3-Akt pathway and or induction of NO by administration of compound or said composition to a mammal in need thereof.

  本发明涉及通式1的化合物，通过抑制PI3-Akt通路和/或诱导NO来治疗恶性肿瘤。本发明还涉及使用通式1的化合物通过抑制PI3-Akt通路和/或诱导NO来治疗恶性肿瘤。本发明还涉及通过向需要该治疗的哺乳动物给予该化合物或该组合物来抑制PI3-Akt通路和/或诱导NO治疗恶性肿瘤的方法。
• INHIBITORS OF PHOSPHATIDYLINOSITOL-3-KINASE (PI3) AND INDUCERS OF NITRIC OXIDE (NO)
  申请人：Bandyopadhyay Santu

  公开号：US20120190738A1

  公开（公告）日：2012-07-26

  The present invention relates to compounds of general formula I for the treatment of malignancy by inhibition of PI3-Akt pathway and or induction of NO. The present invention also relates to the use of compound of general formula I for the treatment of malignancy by inhibition of PI3-Akt pathway and or induction of NO. The present invention further relates to a method of treating malignancy by inhibition of PI3-Akt pathway and or induction of NO by administration of compound or said composition to a mammal in need thereof.

  本发明涉及一般式I的化合物，通过抑制PI3-Akt途径和/或诱导NO治疗恶性肿瘤。本发明还涉及使用一般式I的化合物通过抑制PI3-Akt途径和/或诱导NO治疗恶性肿瘤。本发明还涉及一种通过向需要该治疗的哺乳动物给予化合物或所述组合物来抑制PI3-Akt途径和/或诱导NO治疗恶性肿瘤的方法。
• Insecticide Synergists, 3,4-Methylenedioxyphenoxy Compounds as Synergists for Natural and Synthetic Pyrethrins
  作者：Morton Beroza

  DOI：10.1021/jf60059a002

  日期：1956.1