4-hydroxy-3,5-diiodo-benzaldehyde-oxime | 2296-76-6

• 分子结构分类: 有机化合物 - 苯类化合物 - 酚类
• 英文名称: 4-hydroxy-3,5-diiodo-benzaldehyde-oxime
• 英文别名: 4-Hydroxy-3,5-dijod-benzaldehyd-oxim；4-(Hydroxyiminomethyl)-2,6-diiodophenol
• CAS: 2296-76-6
• 化学式: C₇H₅I₂NO₂
• 分子量: 388.931
• InChiKey: HKHJNPNVZZAURN-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2
• 重原子数：
  12
• 可旋转键数：
  1
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  52.8
• 氢给体数：
  2
• 氢受体数：
  3

安全信息

• 海关编码：
  2928000090

反应信息

• 作为反应物：
  描述：

  4-hydroxy-3,5-diiodo-benzaldehyde-oxime 在 吡啶 、 N-氯代丁二酰亚胺 作用下， 以 四氢呋喃 、 氯仿 为溶剂， 反应 2.0h， 生成
  参考文献：
  名称：

  Discovery of 3-Amino-4-Chlorophenyl P1 as a novel and potent benzamidine mimic via solid-phase synthesis of an isoxazoline library

  摘要：

  In an effort to identify orally bioavailable factor Xa inhibitors, two isoxazolines libraries were prepared to scan for novel P1 ligands. From this work, 4-chloro-3-aniline was identified as a novel and potent benzamidine mimic. (C) 2003 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(03)00130-6
• 作为产物：
  描述：

  3,5-二碘-4-羟基苯甲醛 在 盐酸羟胺 、 sodium acetate 作用下， 以 乙醇 为溶剂， 反应 12.0h， 生成 4-hydroxy-3,5-diiodo-benzaldehyde-oxime
  参考文献：
  名称：

  Discovery of 3-Amino-4-Chlorophenyl P1 as a novel and potent benzamidine mimic via solid-phase synthesis of an isoxazoline library

  摘要：

  In an effort to identify orally bioavailable factor Xa inhibitors, two isoxazolines libraries were prepared to scan for novel P1 ligands. From this work, 4-chloro-3-aniline was identified as a novel and potent benzamidine mimic. (C) 2003 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(03)00130-6

文献信息

• Oxime ethers and pesticidal preparations containing them
  申请人：Ciba-Geigy AG

  公开号：US03941839A1

  公开（公告）日：1976-03-02

  New oxime ethers and pesticidal and herbicidal preparations containing them are disclosed. The oxime ethers correspond to the formula ##SPC1## Wherein R.sub.1 is a hydrogen atom or a lower alkyl radical; R.sub.2 is an aliphatic, cycloaliphatic, araliphatic, aromatic or heterocyclic radical; or wherein R.sub.1 and R.sub.2 form part of a saturated or unsaturated carbocycle or a 5-, 6- or 7-membered heterocycle; R.sub.3 is a nitro, trifluoromethyl, formyl, lower carbalkoxy, sulfamyl or mono- or di-lower alkyl sulfamyl radical; R.sub.4.sub.- and R.sub.5.sub.- each is a hydrogen or halogen atom, an amino, mono- or di-lower alkyl amino, lower alkoxy, cycloalkoxy, lower alkylthio, nitro, lower carbalkoxy, arylthio, lower aralkylthio or lower alkyl group, or 5-, 6- or 7-membered heterocycle.

  揭示了新的肟醚化合物和含有它们的杀虫剂和除草剂制剂。这些肟醚化合物对应于以下结构式：其中R1为氢原子或较低的烷基基团；R2为脂肪族、环脂肪族、芳基脂肪族、芳香族或杂环基团；或者R1和R2构成饱和或不饱和的碳环或5、6或7元杂环的一部分；R3为硝基、三氟甲基、甲酰基、较低的羰基烷氧基、磺胺基或单或双较低的烷基磺胺基基团；R4和R5分别为氢或卤素原子、氨基、单或双较低的烷基氨基、较低的烷氧基、环烷氧基、较低的烷基硫氧基、硝基、较低的羰基烷氧基、芳基硫氧基、较低的芳基烷基硫氧基或较低的烷基基团，或者为5、6或7元杂环。
• Paal; Mohr, Chemische Berichte, 1896, vol. 29, p. 2305
  作者：Paal、Mohr

  DOI：——

  日期：——
• FR1375311
  申请人：——

  公开号：——

  公开（公告）日：——
• Discovery of 3-Amino-4-Chlorophenyl P1 as a novel and potent benzamidine mimic via solid-phase synthesis of an isoxazoline library
  作者：Patrick Y.S. Lam、Jessica J. Adams、Charles G. Clark、W.Jason Calhoun、Joseph M. Luettgen、Robert M. Knabb、Ruth R. Wexler

  DOI：10.1016/s0960-894x(03)00130-6

  日期：2003.5

  In an effort to identify orally bioavailable factor Xa inhibitors, two isoxazolines libraries were prepared to scan for novel P1 ligands. From this work, 4-chloro-3-aniline was identified as a novel and potent benzamidine mimic. (C) 2003 Elsevier Science Ltd. All rights reserved.