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methyl 2-(2-chlorobenzamido)benzoate | 5347-24-0

中文名称
——
中文别名
——
英文名称
methyl 2-(2-chlorobenzamido)benzoate
英文别名
Methyl 2-[(2-chlorobenzoyl)amino]benzoate
methyl 2-(2-chlorobenzamido)benzoate化学式
CAS
5347-24-0
化学式
C15H12ClNO3
mdl
MFCD00791187
分子量
289.718
InChiKey
RVGQWMWLYCVLBF-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):
    3.9
  • 重原子数:
    20
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.07
  • 拓扑面积:
    55.4
  • 氢给体数:
    1
  • 氢受体数:
    3

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • Fungicidal Activity of<i>N</i>-Benzoylanthranilates and Related Compounds
    作者:Osamu Kirino、Shigeo Yamamoto、Toshiro Kato
    DOI:10.1080/00021369.1980.10864289
    日期:1980.9
    Methyl N-(substituted benzoyl)anthranilates were found to possess inhibitory activity against the powdery mildew of cucumber caused by Sphaerotheca fuliginea. Both the anthranilate and the N-benzoyl moieties were essential for this type of fungicidal activity. Substitution at the 2- and 4-positions of the N-benzoyl group was unfavorable to the activity except for the 4-methoxy group. Substitution at the 3-position varied the fungicidal activity to various extents. The variation in the activity of 3-substituted derivatives was analyzed quantitatively with substituent parameters and regression analysis indicating that the variation in the steric dimension of substituents was most responsible for the activity.
    甲基N-(取代苯甲酰基)邻氨基苯甲酸酯被发现对瓜类白粉病具有抑制活性,该病由单丝壳属的真菌引起。邻氨基苯甲酸和N-苯甲酰基对于这种类型的杀菌活性都是必不可少的。N-苯甲酰基的2位和4位取代不利于活性,除非是4-甲氧基。3位取代会以不同程度改变杀菌活性。通过对取代基参数的定量分析和回归分析表明,取代基的空间尺寸变化最能够解释活性的变化。
  • Ag-Catalyzed Practical Synthesis of <i>N</i>-Acyl Anthranilic Acids from Anthranils and Carboxylic Acids
    作者:Changshu Wu、Yang Gao、Yanping Huo、Xianwei Li、Qian Chen、Xiao-Qiang Hu
    DOI:10.1021/acs.joc.3c02586
    日期:2024.3.1
    A practical synthesis of valuable N-acyl anthranilic acids has been achieved via a silver-catalyzed imino-ketene generation from readily available anthranils and carboxylic acids. A wide range of carboxylic acids including sterically demanding aliphatic carboxylic acids, aromatic carboxylic acids, acrylic acids, and amino acids are compatible in this reaction. Moreover, this method can be used to modify
    通过银催化从容易获得的邻氨基苯甲酸和羧酸生成亚氨基乙烯酮,实现了有价值的N-酰基邻氨基苯甲酸的实际合成。多种羧酸,包括空间要求高的脂肪族羧酸、芳香族羧酸、丙烯酸和氨基酸,都适合该反应。此外,该方法还可用于修饰药物分子和天然产物,例如布洛芬、丙磺舒和乙酰甘氨酸。
  • The evaluation and structure–activity relationships of 2-benzoylaminobenzoic esters and their analogues as anti-inflammatory and anti-platelet aggregation agents
    作者:Pei-Wen Hsieh、Tsong-Long Hwang、Chin-Chung Wu、Shin-Zan Chiang、Chung-I Wu、Yang-Chang Wu
    DOI:10.1016/j.bmcl.2006.12.038
    日期:2007.3
    Forty-seven 2-benzoylaminobenzoic esters were synthesized and evaluated in anti-platelet aggregation, inhibition of superoxide anion generation, and inhibition of neutrophil elastase release assays. Most 2-benzoylamino-4-chlorobenzoic acid derivatives showed selective inhibitory effects on arachidonic acid (AA)-induced platelet aggregation. Among them, compounds 615 and 7b exhibited more potent inhibitory effects (ca. 200-fold) than aspirin. Additionally, compounds 1a and 5a showed strong inhibitory effects on neutrophil superoxide generation with IC50 values of 0.65 and 0.17 mu M, respectively. However, compounds 6d and 6e exhibited dual inhibitory effects on platelet aggregation and neutrophil elastase (NE) release; therefore, these two compounds may be new leads for development as anti-inflammatory and anti-platelet aggregatory agents. (c) 2006 Elsevier Ltd. All rights reserved.
  • PAPADOPOULOS, E. P.;TORRES, C. D., HETEROCYCLES, 1982, 19, N 6, 1039-1042
    作者:PAPADOPOULOS, E. P.、TORRES, C. D.
    DOI:——
    日期:——
  • Papadopoulos, Eleftherios P.; Torres, Catherine D., Heterocycles, 1982, vol. 19, # 6, p. 1039 - 1042
    作者:Papadopoulos, Eleftherios P.、Torres, Catherine D.
    DOI:——
    日期:——
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