1-(3-碘丙基)-4-硝基苯 | 100708-34-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 中文名称: 1-(3-碘丙基)-4-硝基苯
• 英文名称: 1-iodo-3-(4-nitrophenyl)propane
• 英文别名: 3-<4-Nitro-phenyl>-propyliodid；3-Jod-1-<4-nitro-phenyl>-propan；1-(3-iodopropyl)-4-nitrobenzene
• CAS: 100708-34-7
• 化学式: C₉H₁₀INO₂
• 分子量: 291.088
• InChiKey: KYIJVKCAHAAZMU-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.2
• 重原子数：
  13
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  45.8
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  1-(3-碘丙基)-4-硝基苯 在 silver nitrate 作用下， 以 1,4-二氧六环 、 水 为溶剂， 反应 2.0h， 以52%的产率得到3-(4-硝基苯基)-1-丙醇
  参考文献：
  名称：

  Photochemical Synthesis of Aldehydes in the Solid Phase

  摘要：

  A substituted anthraquinone (AQ), previously shown to photochemically generate benzaldehyde in methanol solution, was attached to a commercially available resin via an I I carbon tether and an amide bond. Photolysis of the polymer-bound AQ with visible or 350 nm UV light resulted in the formation of benzaldehyde in yields of 50-55% as determined by HPLC. The phenolic positions in the polymer were then alkylated using benzyl bromide and 1-iodo-3-(4-nitrophctiyl)propane in a coupling reaction with K2CO3 as a base and a solution-phase proton shuttle. Photolysis of these alkylated polymers resulted in the formation of benzaldehyde (54-89%) and 3-(4-nitrophenyl)propanal (58-67%). The yields of both aldehydes dropped considerably with subsequent realkylation and photolysis, and the polymer beads began to show signs of deterioration. This is the first time that aldehydes have been made photochemically on a solid-supported phase.

  DOI：

  10.1021/jo025508u
• 作为产物：
  描述：

  对硝基肉桂酸 在 咪唑 、 锂硼氢 、 正癸烯 、 硫酸 、 碘 、 三苯基膦 作用下， 以 四氢呋喃 、 甲苯 为溶剂， 反应 22.5h， 生成 1-(3-碘丙基)-4-硝基苯
  参考文献：
  名称：

  对-叠氮基苯基-2-苯基链烷酸乙酯分子内环化合成四氢萘木质素酯及其对人肿瘤细胞系生长抑制的评价

  摘要：

  通过带有末端对-叠氮基苯基的2-苯基戊酸/ 2-苯基丁酸酸酯的氮离子的分子内环化作用可直接获得四氢萘木脂酸酯。所述p -azidophenyl取代丁酸乙酯导致乙基spirodienone羧酸盐，而其同系物，得到戊4-（4-氨基苯基）以良好收率-1,2,3,4-四氢化萘-1-羧酸叔丁酯。与此相反，米-叠氮基苯基取代的酯遭受三氟甲烷磺酸的芳族亲核加成。X射线晶体学明确地确定了最终产物的结构，并进行了密度泛函理论研究以合理化环化结果。评价了反应中间体和终产物抑制MCF-7（乳腺癌），NCI-H460（肺癌），SF-268（CNS癌症）和UACC-62（黑素瘤）细胞系体外生长的能力。 。用的spirodienone羧酸盐，所观察到的乳腺癌，肺癌，和CNS癌细胞系的生长抑制米-nitrophenylalkyl碘化物，和p -苯基-取代的细长乙酯，即p -nitrophenylpentanoate和p

  DOI：

  10.1021/jm101182s

文献信息

• NOVEL DIAMINE, POLYAMIC ACID, AND POLYIMIDE
  申请人：NISSAN CHEMICAL INDUSTRIES. LTD.

  公开号：US20160264520A1

  公开（公告）日：2016-09-15

  To provide a novel diamine, and a polyimide precursor and a polyimide using it. A diamine represented by the formula (1): wherein each of X 1 and X 5 which are independent of each other, is a single bond or the like; each of X 2 and X 4 which are independent of each other, is —CH 2 — or the like; X 3 is a C 1-6 alkylene or the like; each of Y 1 and Y 2 which are independent of each other, is a single bond or the like; R is a C 1-20 linear, branched or cyclic hydrocarbon group; and a is 0 or 1).

  提供一种新颖的二胺，以及使用它的聚酰亚胺前体和聚酰亚胺。一种由式（1）表示的二胺：其中X1和X5中的每一个独立的，是单键或类似物；X2和X4中的每一个独立的，是—CH2—或类似物；X3是C1-6烷基或类似物；Y1和Y2中的每一个独立的，是单键或类似物；R是C1-20线性、支链或环烃基；a为0或1。
• Diamine, polyamic acid, and polyimide
  申请人：NISSAN CHEMICAL INDUSTRIES, LTD.

  公开号：US10023530B2

  公开（公告）日：2018-07-17

  To provide a novel diamine, and a polyimide precursor and a polyimide using it. A diamine represented by the formula (1): wherein each of X1 and X5 which are independent of each other, is a single bond or the like; each of X2 and X4 which are independent of each other, is —CH2— or the like; X3 is a C1-6 alkylene or the like; each of Y1 and Y2 which are independent of each other, is a single bond or the like; R is a C1-20 linear, branched or cyclic hydrocarbon group; and a is 0 or 1).

  提供一种新型二胺、一种聚酰亚胺前体和一种使用该二胺的聚酰亚胺。由式（1）表示的二胺： 其中相互独立的 X1 和 X5 各为单键或类似物；相互独立的 X2 和 X4 各为-CH2-或类似物；X3 为 C1-6 亚烷基或类似物；相互独立的 Y1 和 Y2 各为单键或类似物；R 为 C1-20 直链、支链或环状烃基；a 为 0 或 1）。
• DNA-directed alkylating agents. 2. Synthesis and biological activity of platinum complexes linked to 9-anilinoacridine
  作者：Brian D. Palmer、Ho H. Lee、Paul Johnson、Bruce C. Baguley、Geoffrey Wickham、Laurence P. G. Wakelin、W. David McFadyen、William A. Denny

  DOI：10.1021/jm00173a015

  日期：1990.11

  Two different classes of cis-diaminedichloroplatinum(II) complexes linked to the DNA-intercalating chromophore 9-anilinoacridine have been synthesized and evaluated as DNA-targeted antitumor agents. Two different Pt chelating ligands were investigated (based on 1,2-ethanediamine and 1,3-propanediamine), designed to deliver the Pt in an orientation likely to respectively enhance either intrastrand or interstrand cross-linking. Although both sets of ligands were somewhat unstable under neutral or basic conditions with respect to disproportionation, the corresponding Pt complexes, once prepared, appeared to be quite stable. All the Pt complexes were monitored for purity by TLC, HPLC, and FAB mass spectra, and the mode of Pt coordination was established by 195Pt NMR spectroscopy. The complexes appeared to cause simultaneous platination and intercalative unwinding of plasmid DNA. In vitro studies were carried out with both wild-type and cisplatin-resistant P388 cell lines. Whereas cisplatin itself and the ethylenediamine and 1,3-propanediamine complexes used as standards were about 10-fold less active against the resistant line, the ethylenediamine-linked Pt complexes showed no differential toxicity between the two lines and the propanediamine-linked complexes showed significant differentials (up to 8-fold) in favor of the cisplatin-resistant line. However, these were no greater than those shown by the unplatinated ligands themselves. The majority of the acridine complexes were inactive in vivo against the wild-type P388 leukemia. They were very insoluble, and although a suitable formulation was found, this may have been a factor. It is also possible that these compounds bind in such a way as to direct the Pt away from the major groove.
• Iliceto,A. et al., Gazzetta Chimica Italiana, 1960, vol. 90, p. 660 - 670
  作者：Iliceto,A. et al.

  DOI：——

  日期：——
• Photochemical Synthesis of Aldehydes in the Solid Phase
  作者：Ronald L Blankespoor、Tim DeVries、Eric Hansen、Jeffrey M. Kallemeyn、Aaron M. Klooster、Jason A. Mulder、Robert P. Smart、Douglas A. Vander Griend

  DOI：10.1021/jo025508u

  日期：2002.4.1

  A substituted anthraquinone (AQ), previously shown to photochemically generate benzaldehyde in methanol solution, was attached to a commercially available resin via an I I carbon tether and an amide bond. Photolysis of the polymer-bound AQ with visible or 350 nm UV light resulted in the formation of benzaldehyde in yields of 50-55% as determined by HPLC. The phenolic positions in the polymer were then alkylated using benzyl bromide and 1-iodo-3-(4-nitrophctiyl)propane in a coupling reaction with K2CO3 as a base and a solution-phase proton shuttle. Photolysis of these alkylated polymers resulted in the formation of benzaldehyde (54-89%) and 3-(4-nitrophenyl)propanal (58-67%). The yields of both aldehydes dropped considerably with subsequent realkylation and photolysis, and the polymer beads began to show signs of deterioration. This is the first time that aldehydes have been made photochemically on a solid-supported phase.