4-乙酰基苯基氨基甲酸酯 | 63082-10-0

• 分子结构分类: 有机化合物 - 有机氧化合物
• 中文名称: 4-乙酰基苯基氨基甲酸酯
• 英文名称: 4-acetylphenyl carbamate
• 英文别名: (4-Acetylphenyl) carbamate
• CAS: 63082-10-0
• 化学式: C₉H₉NO₃
• 分子量: 179.175
• InChiKey: AONZOVFDPMYHTL-UHFFFAOYSA-N

物化性质

• 沸点：
  374.3±34.0 °C(Predicted)
• 密度：
  1.229±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  0.7
• 重原子数：
  13
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.11
• 拓扑面积：
  69.4
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  氯磺酰异氰酸酯 、 对羟基苯乙酮 生成 4-乙酰基苯基氨基甲酸酯
  参考文献：
  名称：

  Elimination-addition mechanisms of acyl group transfer: the hydrolysis and synthesis of carbamates

  摘要：

  DOI：

  10.1021/ja00450a045

文献信息

• [EN] FACTOR XIa INHIBITORS<br/>[FR] INHIBITEURS DU FACTEUR XIA
  申请人：MERCK SHARP & DOHME

  公开号：WO2016015593A1

  公开（公告）日：2016-02-04

  The present invention provides a compound of Formula (I) and pharmaceutical compositions comprising one or more said compounds, and methods for using said compounds for treating or preventing thromboses, embolisms, hypercoagulability or fibrotic changes. The compounds are selective Factor XIa inhibitors or dual inhibitors of Factor XIa and plasma kallikrein.

  本发明提供了一种化合物(I)及包含一种或多种所述化合物的药物组合物，以及使用所述化合物用于治疗或预防血栓、栓塞、高凝血性或纤维变化的方法。这些化合物是选择性因子XIa抑制剂或因子XIa和血浆激肽原的双重抑制剂。
• Aroylnitrenes with singlet ground states: photochemistry of acetyl-substituted aroyl and aryloxycarbonyl azides
  作者：Michael E. Sigman、Tom. Autrey、Gary B. Schuster

  DOI：10.1021/ja00221a032

  日期：1988.6

  light gives only the aroylnitrenes. The triplet excited states of the azides were detected chemically and by transient spectroscopic techniques. Nitrogen loss following near-UV irradiation occurs exclusively from the excited triplet azides. However, the chemical properties of ABN and ADN are consistent only with reactions originating from their singlet states. An ESR spectrum is observed at 8 K for

  4-乙酰苯甲酰叠氮化物 (ABA)、4-乙酰-4'-联苯酰叠氮化物 (ADA) 和 4-乙酰苯氧羰基叠氮化物 (APA) 的光化学显示出不寻常的波长和结构效应。用深紫外光将 ABA 或 ADA 辐照到它们的 ..pi..-..pi..* 带中，分别导致 4-乙酰苯甲酰氮 (ABN) 和 4-乙酰-4'-联苯甲酰氮 (ADN) 的形成，与光库尔修斯重排竞争形成异氰酸酯。用近紫外光将这些叠氮化物照射到它们的 n-..pi..* 带中，仅产生芳酰基硝烯。叠氮化物的三重激发态通过化学方法和瞬态光谱技术进行检测。近紫外线照射后的氮损失仅发生在激发的三重叠氮化物上。然而，ABN 和 ADN 的化学性质仅与源自其单线态的反应一致。在 8 K 处观察到 ((4-乙酰苯氧基) 羰基) 氮烯 (APN) 的 ESR 谱，但 4-乙酰苯甲酰基氮 (ABN) 或 4-乙酰-4'-联苯羰基氮 (ADN) 没有。AP
• COMPOSITIONS FOR DECREASING ACTIVITY OF HORMONE-SENSITIVE LIPASE
  申请人：NOVO NORDISK A/S

  公开号：EP1458375A2

  公开（公告）日：2004-09-22
• FACTOR XIa INHIBITORS
  申请人：Merck Sharp & Dohme Corp.

  公开号：EP3180317A1

  公开（公告）日：2017-06-21
• [EN] COMPOUNDS AND USE THEREOF FOR DECREASING ACTIVITY OF HORMONE-SENSITIVE LIPASE<br/>[FR] UTILISATION DE COMPOSES POUR REDUIRE L'ACTIVITE DE LA LIPASE HORMONO-SENSIBLE
  申请人：NOVO NORDISK AS

  公开号：WO2003051842A2

  公开（公告）日：2003-06-26

  Carbamates and related compounds of formula R1R2NCO-Y or R1R2NCS-Y wherein R1 and R2 may form a ring, are inhibitors of hormone sensitive lipase and are useful for the treatment of any disorder where it is desirable to modulate the plasma level of free fatty acids, glycerol, LDL-cholesterol, HDL-cholesterol, insulin and/or glucose; and or modulate intracellular triacylglycerol and cholesterol stores, intracellular level of fatty acids, fatty acid esters such as diacylglycerols, phosphatidic acids, long chain acyl-CoA’s as well as citrate or malonyl-CoA; and or increase insulin sensitivity; and or modulate insulin secretion from pancreatic beta cells. More particularly said disorders are selected from the group consisting of insulin resistance, diabetes type 1, hyperglycemia, dislipidemia, obesity, abnormalities of lipoprotein metabolism and any combinations thereof.