摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

3-氯哌啶-2-酮 | 16834-22-3

中文名称
3-氯哌啶-2-酮
中文别名
——
英文名称
3-chloro-piperidin-2-one
英文别名
α-Chlor-δ-valerolactam;3-Chloropiperidin-2-one
3-氯哌啶-2-酮化学式
CAS
16834-22-3
化学式
C5H8ClNO
mdl
MFCD13178830
分子量
133.578
InChiKey
PAZWVXFBGNCTJQ-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    0.7
  • 重原子数:
    8
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.8
  • 拓扑面积:
    29.1
  • 氢给体数:
    1
  • 氢受体数:
    1

SDS

SDS:fc6f2f056b7c25efae33ad4195f6df95
查看

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    参考文献:
    名称:
    Novel non-trimethoxylphenyl piperlongumine derivatives selectively kill cancer cells
    摘要:
    Piperlongumine (PL) is a natural alkaloid with broad biological activities. Twelve analogues have been designed and synthesized with non-substituted benzyl rings or heterocycles in this work. Most of the compounds showed better anticancer activities than the parent PL without apparent toxicity in normal cells. Elevation of cellular ROS levels was one of the main anticancer mechanisms of these compounds. Cell apoptosis and cell cycle arrest for the best compound ZM90 were evaluated and similar mechanism of action with PL was demonstrated. The SAR was also characterized, providing worthy directions for further optimization of PL compounds. (C) 2017 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2017.04.035
  • 作为产物:
    描述:
    L-鸟氨酸盐酸盐盐酸aluminum oxidesodium hydroxide溶剂黄146亚硝酸异戊酯 作用下, 以 1,4-二氧六环氯仿甲苯 为溶剂, 反应 2.75h, 生成 3-氯哌啶-2-酮
    参考文献:
    名称:
    3-重氮哌啶-2-酮的合成与化学
    摘要:
    据报道,从1-鸟氨酸中分两步有效地合成了3-重氮-哌啶-2-酮。探索了这种新的环状α-重氮酰胺的化学性质,并可以快速获得各种3-取代的哌啶-2-酮衍生物。
    DOI:
    10.1016/s0040-4020(02)00278-8
点击查看最新优质反应信息

文献信息

  • DERIVATIVES OF PIPERLONGUMINE AND USES THEREOF
    申请人:Auransa Inc.
    公开号:US20200377510A1
    公开(公告)日:2020-12-03
    The present invention relates to a group of 1-[(E)-3-(3,4,5-trimethoxyphenyl)prop-2-enoyl]-2,3-dihydropyridin-6-one (piperlongumine) derivatives, analogs and pharmaceutically acceptable salts thereof. The present invention also relates to a pharmaceutical composition and formulation containing a derivative of piperlongumine; and use of the derivatives and analogs for treating cancer, reducing inflammation and/or treating an autoimmune or inflammatory disease.
    本发明涉及一组1-[(E)-3-(3,4,5-三甲氧基苯基)丙-2-烯酰基]-2,3-二氢吡啶-6-酮(长椒碱)衍生物、类似物及其药学上可接受的盐。本发明还涉及含有长椒碱衍生物的药物组合物和配方;以及利用这些衍生物和类似物治疗癌症、减少炎症和/或治疗自身免疫或炎症性疾病。
  • Method for producing organic compounds by substituting halogen atoms
    申请人:MITSUI CHEMICALS, INC.
    公开号:EP1486479A1
    公开(公告)日:2004-12-15
    The invention pertains to a method in which a halogen atom of an organic compound is replaced with a group derived from a nucleophilic agent, at high yield and high efficiency, by the following method which includes a step of reacting the nucleophilic agent with an organic material having a halogen atom bonded to a carbon atom having four σ bonds, more specifically: a method for producing an organic compound having Q, the method including a step of reacting a compound represented by general formula (2) with an organic starting material having at least one halogen atom bonded to a carbon atom having four σ bonds so as to replace the halogen atom in the organic starting material with Q:         MQa     (2) (wherein M represents an alkali metal atom, an alkali earth metal atom, or a rare earth metal atom; Q represents a moiety of an inorganic acid or an active hydrogen compound derived by eliminating a proton, wherein Q is a halogen atom different from the halogen atom in the organic starting material having the halogen atom bonded to the carbon atom having the four σ bonds; and a represents an integer of 1 to 3) in the presence of a compound represented by general formula (1) (wherein Z- represents an anion derived by eliminating a proton from an inorganic acid or an active hydrogen compound; R2 is the same or different; R2 each independently represent a C1-C10 hydrocarbon group or two R2 on the same nitrogen atom may be bonded with each other to form a ring with the nitrogen atom).
    这项发明涉及一种方法,其中有机化合物中的卤素原子被来自亲核试剂的基团取代,且产率高效率高,通过以下方法实现,包括以下步骤:将亲核试剂与具有与碳原子形成四个σ键的卤素原子相结合的有机材料反应的步骤,更具体地说:一种用于生产具有Q的有机化合物的方法,包括以下步骤:将由通式(2)表示的化合物与至少一个卤素原子与碳原子形成四个σ键的有机起始材料反应,以将有机起始材料中的卤素原子替换为Q:         MQa     (2) (其中M代表碱金属原子、碱土金属原子或稀土金属原子;Q代表由消除质子衍生的无机酸或活性氢化合物的基团,其中Q是不同于有机起始材料中卤素原子的卤素原子,该卤素原子与具有四个σ键的碳原子相结合;a表示1到3的整数),在通式(1)表示的化合物的存在下 (其中Z-代表由无机酸或活性氢化合物中消除质子衍生的阴离子;R2相同或不同;R2各自独立地表示C1-C10烃基,或者两个R2在同一氮原子上可能与彼此结合形成与氮原子的环)。
  • MID-CHAIN BRANCHED PERACIDS AND PERACID PRECURSORS
    申请人:——
    公开号:US20020161258A1
    公开(公告)日:2002-10-31
    Mid-chain branched peracids and peracid precursors useful in laundry and cleaning compositions, especially granular and liquid detergent compositions are disclosed. These peracids and precursors are suitable for formulation with a wide range of detergent adjuncts for the purpose of providing improved cleaning systems, especially for use in detergent compositions which will be used in laundry processes involving low water temperature wash conditions. The present invention also relates to novel mid-chain branched peracids and precursors for use in the compositions of the present invention.
    本发明涉及中链支化过酸和过酸前体,用于洗涤和清洁组合物,特别是颗粒和液体洗涤剂组合物。这些过酸和前体适用于与各种洗涤剂助剂配方,以提供改进的清洁系统,特别是用于洗涤剂组合物中,该组合物将用于涉及低水温洗涤条件的洗涤过程。本发明还涉及用于本发明组合物的新型中链支化过酸和前体。
  • Compositions comprising XET and a polysaccharide and/or oligosaccharide
    申请人:The Procter & Gamble Company
    公开号:US20020151451A1
    公开(公告)日:2002-10-17
    The present invention relates to laundry and/or fabric and/or color care compositions; more particularly, to laundry and/or fabric and/or color care compositions containing xyloglucan endotransglycosylase enzyme (XET) in combination with a polysaccharide and/or oligosaccharide, preferably a xyloglucan polymer, that provide improved anti-wrinkle and/or shape retention and/or anti-shrinkage and/or tensile strength and/or color appearance and/or anti-bobbling and/or better static control, fabric softness, anti-wear properties and benefits, while at the same time providing improved cleaning benefits, over laundry and/or fabric and/or color care compositions without such combination of XET and polysaccharide and/or oligosaccharide.
    本发明涉及洗衣和/或织物和/或色彩护理组合物;本发明涉及洗衣和/或织物和/或色彩护理组合物;更具体地说,涉及含有木聚糖内切糖基化酶(XET)与多糖和/或低聚糖(最好是木聚糖聚合物)组合的洗衣和/或织物和/或色彩护理组合物,该组合物具有更好的抗皱和/或保形和/或防缩和/或拉伸强度和/或色彩外观和/或防晃动和/或更好的静电控制、织物柔软度、抗磨损性能和优点,同时提供更好的清洁效果。
  • Method for producing organic compound by substituting halogen atoms
    申请人:Mitsui Chemicals, Inc.
    公开号:US20040256743A1
    公开(公告)日:2004-12-23
    A method for producing an organic compound having Q, the method including a step of reacting a compound represented by general formula (2) with an organic starting material having at least one halogen atom bonded to a carbon atom having four &sgr; bonds so as to replace the halogen atom in the organic starting material with Q: MQ a (2) wherein M, Q and a are defined in the presence of a compound represented by general formula (1) 1 wherein Z − and Rs are also defined.
    一种生产具有 Q 的有机化合物的方法,该方法包括以下步骤:将通式(2)代表的化合物与有机起始材料反应,该有机起始材料具有至少一个与具有四个&sgr;键的碳原子成键的卤原子,从而用 Q 取代有机起始材料中的卤原子: MQ a (2) 其中 M、Q 和 a 是在通式(1)所代表的化合物存在时定义的 1 其中 Z - 和 Rs 也已定义。
查看更多