94514-21-3 (4-氟邻苯二甲酰亚胺,5-fluoro-2,3-dihydro-1H-isoindole-1,3-dione)

CAS号:
94514-21-3
中文名称:
4-氟邻苯二甲酰亚胺
英文名称:
5-fluoro-2,3-dihydro-1H-isoindole-1,3-dione
分子式:
C8H4FNO2
分子量:
165.121265411377

4-氟邻苯二甲酰亚胺(94514-21-3)名称与标识符

名称

中文别名:
4-氟邻苯二甲酰亚胺;5-氟-1H-异吲哚-1,3(2H)-二酮;
英文别名:
5-fluoro-1H-Isoindole-1,3(2H)-dione;1H-Isoindole-1,3(2H)-dione, 5-fluoro-;4-FLUOROPHTHALIMIDE;5-Fluoro-1H-isoindole-1,3(2H)-dione (ACI);5-Fluoro-isoindole-1,3-dione;5-Fluoroisoindoline-1,3-dione;5-fluoro-2,3-dihydro-1H-isoindole-1,3-dione;Z1255487934;AKOS005067070;GS3910;CS-0058047;94514-21-3;DVDRUQOUGHIYCB-UHFFFAOYSA-N;EN300-99458;5-FLUORO-2H-ISOINDOLE-1,3-DIONE;MFCD00627750;SB23057;D84570;SCHEMBL1953630;UNII-HF76654PW9;5-fluoroisoindole-1,3-dione;HF76654PW9;

标识符

MDL:
MFCD00627750
InChIKey:
DVDRUQOUGHIYCB-UHFFFAOYSA-N
Inchi:
1S/C8H4FNO2/c9-4-1-2-5-6(3-4)8(12)10-7(5)11/h1-3H,(H,10,11,12)
SMILES:
O=C1C2C(=CC(=CC=2)F)C(=O)N1

4-氟邻苯二甲酰亚胺(94514-21-3)物化性质

计算特性

  • 精确分子量 : 165.02260653 g/mol
  • 氢键供体数量 : 1
  • 氢键受体数量 : 3
  • 可旋转化学键数量 : 0
  • 同位素质量 : 165.02260653 g/mol
  • 重原子数量 : 12
  • 复杂度 : 241
  • 同位素原子数量 : 0
  • 确定原子立构中心数量 : 0
  • 不确定原子立构中心数量 : 0
  • 确定化学键立构中心数量 : 0
  • 不确定化学键立构中心数量 : 0
  • 共价键单元数量 : 1
  • 疏水参数计算参考值(XlogP) : 1.3
  • 拓扑分子极性表面积 : 46.2Ų
  • 分子量 : 165.12

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4-氟邻苯二甲酰亚胺(94514-21-3)合成路线

合成路线:1 步
反应条件:
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Benzimidazole derivatives as inhibitors of leukotriene production and their preparation and use for the treatment of leukotriene-mediated diseases
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Preparation of heterocyclic substituted phenyl methanones as inhibitors of the glycine transporter 1
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Preparation of pyrazolopyridines, pyrazolopyrimidines and related compounds for inhibiting plasma kallikrein
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Method for synthesizing phthalimide and benzene ring-substituted derivative thereof
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Copper(II)-dioxygen facilitated activation of nitromethane: nitrogen donors for the synthesis of substituted 2-hydroxyimino-2-phenylacetonitriles and phthalimides
Xiang, Shiqun; Li, Yinghua; Fan, Weibin; Jin, Jiang; Zhang, Wei; et al, Frontiers in Chemistry (Lausanne, 2020, 8,
合成路线:1 步
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Mechanistic Studies on the Organocatalytic α-Chlorination of Aldehydes: The Role and Nature of Off-Cycle Intermediates
Ponath, Sebastian; Menger, Martina; Grothues, Lydia; Weber, Manuela; Lentz, Dieter; et al, Angewandte Chemie, 2018, 57(36), 11683-11687
合成路线:1 步
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Synthesis, photophysical and thermal properties of 2,9,16,23-tetrafluoro substituted metallophthalocyanines
Li, J.; Li, X. G.; Xiao, Y.; Wang, S. R., Materials Research Innovations, 2014, 18(5), 340-345
合成路线:1 步
反应条件:
参考文献:
Synthesis of 4-fluorophthalimide by Balz-Schieman
Li, Jian; Exiu, Tian-feng; Wang, Shi-rong; Xiao, Yin; Hu, Ya-qin, Jingxi Huagong, 2013, 30(9), 1077-1080
合成路线:1 步
反应条件:
参考文献:
Direct Access to Cobaltacycles via C-H Activation: N-Chloroamide-Enabled Room-Temperature Synthesis of Heterocycles
Yu, Xiaolong; Chen, Kehao; Guo, Shan; Shi, Pengfei; Song, Chao; et al, Organic Letters, 2017, 19(19), 5348-5351
合成路线:1 步
反应条件:
参考文献:
Preparation of substituted benzo[d]imidazo[2,1-b]thiazole-7-carboxamides as c-MYC mRNA translation modulators and uses thereof in the treatment of cancer
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合成路线:1 步
反应条件:
参考文献:
Inhibitors of dipeptidyl peptidase 8 and dipeptidyl peptidase 9. Part 2: Isoindoline containing inhibitors
Van Goethem, Sebastiaan; Van der Veken, Pieter; Dubois, Veronique; Soroka, Anna; Lambeir, Anne-Marie; et al, Bioorganic & Medicinal Chemistry Letters, 2008, 18(14), 4159-4162
合成路线:1 步
参考文献:
Fluorophthalimides
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