2-三氟甲硫基苯甲醛 | 57830-48-5

• 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: 2-三氟甲硫基苯甲醛
• 中文别名: 2-(三氟甲基硫代)苯甲醛
• 英文名称: 2-((trifluoromethyl)thio)benzaldehyde
• 英文别名: 2-(Trifluoromethylthio)benzaldehyde；2-(trifluoromethylsulfanyl)benzaldehyde
• CAS: 57830-48-5
• 化学式: C₈H₅F₃OS
• mdl: MFCD00236334
• 分子量: 206.188
• InChiKey: JQSKYLMRBFOYTR-UHFFFAOYSA-N

物化性质

• 沸点：
  168.6±40.0 °C(Predicted)
• 密度：
  1.37±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.1
• 重原子数：
  13
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.125
• 拓扑面积：
  42.4
• 氢给体数：
  0
• 氢受体数：
  5

安全信息

• 危险品标志：
  Xi
• 危险类别码：
  R36/37/38
• 海关编码：
  2930909090
• 安全说明：
  S26,S36

反应信息

• 作为反应物：
  描述：

  2-三氟甲硫基苯甲醛 在 硫酸 作用下， 反应 18.25h， 以31%的产率得到5-nitro-2-(trifluoromethylthio)benzaldehyde
  参考文献：
  名称：

  [EN] MACROCYCLIC FACTOR VIIA INHIBITORS
  [FR] INHIBITEURS DU FACTEUR VIIA MACROCYCLIQUES

  摘要：

  公开号：

  WO2014201073A9
• 作为产物：
  描述：

  N-(2-iodobenzylidene)aniline 在 盐酸 、 1,10-菲罗啉 、 copper(I) bromide 作用下， 以 水 、 N,N-二甲基甲酰胺 为溶剂， 反应 6.0h， 生成 2-三氟甲硫基苯甲醛
  参考文献：
  名称：

  Copper-Catalyzed Trifluoromethylthiolation of Aryl Halides with Diverse Directing Groups

  摘要：

  The expansion of cross-coupling components in Cu-catalyzed C-X bond forming reactions have received much attention recently. A novel Cu-catalyzed trifluoromethylthiolation of aryl bromides and iodides with the assistance of versatile directing groups such as pyridyl, methyl ester, amide, imine and oxime was reported. CuBr was used as the catalyst, and 1,10-phenanthroline as the ligand. By changing the solvent from acetonitrile to DMF, the coupling process could even take place at room temperature.

  DOI：

  10.1021/ol501742a

文献信息

• (R)-chiral halogenated substituted N-benzyl-N-phenyl aminoalcohol compounds useful for inhibiting cholesteryl ester transfer protein activity
  申请人：——

  公开号：US20020177708A1

  公开（公告）日：2002-11-28

  The invention relates to substituted aryl and heteroaryl (R)-Chiral Halogenated 1-Substitutedamino-(n+1)-Alkanol compounds useful as inhibitors of cholesteryl ester transfer protein (CETP; plasma lipid transfer protein-I) and compounds, compositions and methods for treating atherosclerosis and other coronary artery diseases. Novel high yield, stereoselective processes for the preparation of the chiral substituted alkanol compounds from chiral and achiral intermediates are described.

  这项发明涉及取代芳基和杂环芳基的(R)-手性卤代1-取代氨基-(n+1)-烷醇化合物，用作胆固醇酯转移蛋白(CETP；血浆脂质转移蛋白-I)的抑制剂，以及用于治疗动脉粥样硬化和其他冠状动脉疾病的化合物、组合物和方法。描述了从手性和不对映体中间体制备手性取代烷醇化合物的新型高产率、立体选择性过程。
• Substituted 1, 4-thiazepine and analogs as activators of caspases and inducers of apoptosis and the use thereof
  申请人：Cytovia, Inc.

  公开号：US20020010169A1

  公开（公告）日：2002-01-24

  The present invention is directed to substituted 1,4-thiazepine and analogs thereof, represented by the general Formula I: 1 wherein the dashed lines, A 1 , A 2 , A 3 , X 1 and R 1 are defined herein. The present invention also relates to the discovery that compounds having Formula I are activators of capases and inducers of apoptosis. Therefore, the activators of caspases and inducers of apoptosis of this invention can be used to induce cell death in a variety of clinical conditions in which uncontrolled growth and spread of abnormal cells occurs.

  本发明涉及被一般式I表示的取代的1,4-噻吩和其类似物，其中虚线、A1、A2、A3、X1和R1在此处被定义。本发明还涉及发现具有式I的化合物是卡泊酶激活剂和凋亡诱导剂。因此，本发明的卡泊酶激活剂和凋亡诱导剂可用于诱导在各种临床病况中发生细胞死亡，其中异常细胞的不受控制的生长和扩散。
• Light- and Thermal-Activated Olefin Metathesis of Hindered Substrates
  作者：Elisa Ivry、Alexander Frenklah、Yakov Ginzburg、Efrat Levin、Israel Goldberg、Sebastian Kozuch、N. Gabriel Lemcoff、Eyal Tzur

  DOI：10.1021/acs.organomet.7b00677

  日期：2018.1.22

  metathesis reactions of tetra-substituted olefins were obtained by the S-chelated ruthenium precatalyst Tol-SCF3. Its reactivity in a series of benchmark olefin metathesis reactions was compared to previously reported Mes-SCF3 and a novel sterically congested S-chelated complex, Dipp-SCF3. Tol-SCF3 is thus the first latent catalyst proven to be capable of promoting olefin metathesis of demanding substrates

  通过S螯合的钌预催化剂Tol-SCF 3获得了四取代烯烃的有效的光活化和热活化复分解反应。将其在一系列基准烯烃复分解反应中的反应性与先前报道的Mes-SCF 3和新型空间拥挤的S螯合复合物Dipp-SCF 3进行了比较。因此，Tol-SCF 3是第一种潜在催化剂，被证明能够在室温下刺激光后促进所需底物的烯烃复分解。
• Ligandless Nickel-Catalyzed <i>Ortho</i>-Selective Directed Trifluoromethylthiolation of Aryl Chlorides and Bromides Using AgSCF₃
  作者：Tin Nguyen、Weiling Chiu、Xinying Wang、Madeleine O. Sattler、Jennifer A. Love

  DOI：10.1021/acs.orglett.6b02689

  日期：2016.11.4

  A mild protocol for Ni-catalyzed trifluoromethylthiolation of aryl chlorides and bromides is described herein. The method utilizes AgSCF3 as an easily accessible nucleophilic trifluoromethylthiolating reagent and does not require any ligands or additives. Ortho-selectivity is achieved using a variety of directing groups such as imines, pyridines, and oxazolines for 24 examples in up to 95% yield.

  本文描述了Ni催化的芳基氯化物和溴化物的三氟甲基硫醇化的温和方案。该方法利用AgSCF 3作为容易获得的亲核三氟甲基硫醇化试剂，不需要任何配体或添加剂。对于24个实例，使用多种指导基团如亚胺，吡啶和恶唑啉实现邻位选择性，产率高达95％。
• Discovery and optimization of a novel Neuromedin B receptor antagonist
  作者：Jiasheng Fu、Stephen J. Shuttleworth、Richard V. Connors、Anne Chai、Peter Coward

  DOI：10.1016/j.bmcl.2009.05.124

  日期：2009.8

  The discovery and parallel synthesis of potent, small molecule antagonists of Neuromedin B receptor based on the ary-hexahydro-dibenzodiazepin-1-one core is described.

  描述和发现了基于ary-hexahydro-dibenzodiazepin-1-one核心的Neuromedin B受体的有效小分子拮抗剂并进行了平行合成。