13720-91-7 (4-乙氧基喹啉,4-Ethoxyquinoline)

CAS号:
13720-91-7
中文名称:
4-乙氧基喹啉
英文名称:
4-Ethoxyquinoline
分子式:
C11H11NO
分子量:
173.211142778397

4-乙氧基喹啉(13720-91-7)名称与标识符

名称

中文别名:
4-乙氧基喹啉;
英文别名:
4-Ethoxyquinoline;4-ETHOXY-QUINOLINE;Quinoline, 4-ethoxy-;4-Aethoxy-chinolin;4-Ethoxy-chinolin;NBAWYUCPNKZTER-UHFFFAOYSA;Quinoline,4-ethoxy;SCHEMBL526387;AKOS006274463;13720-91-7;NBAWYUCPNKZTER-UHFFFAOYSA-;InChI=1/C11H11NO/c1-2-13-11-7-8-12-10-6-4-3-5-9(10)11/h3-8H,2H2,1H3;AC-20565;Quinoline,4-ethoxy-;DTXSID10160104;

标识符

InChIKey:
NBAWYUCPNKZTER-UHFFFAOYSA-N
Inchi:
1S/C11H11NO/c1-2-13-11-7-8-12-10-6-4-3-5-9(10)11/h3-8H,2H2,1H3
SMILES:
O(CC)C1C=CN=C2C=CC=CC=12

4-乙氧基喹啉(13720-91-7)物化性质

实验特性

  • LogP : 2.63350
  • PSA : 22.12000

计算特性

  • 精确分子量 : 173.08400
  • 氢键供体数量 : 0
  • 氢键受体数量 : 2
  • 可旋转化学键数量 : 2
  • 同位素质量 : 173.084063974g/mol
  • 重原子数量 : 13
  • 复杂度 : 160
  • 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 : 22.1Ų

4-乙氧基喹啉(13720-91-7)海关数据

海关编码:
2933499090
海关数据:

中国海关编码:

2933499090

概述:

2933499090. 其他含喹琳或异喹啉环系的化合物〔但未进一步稠合的〕. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:20.0%

申报要素:

品名, 成分含量, 用途, 乌洛托品请注明外观, 6-己内酰胺请注明外观, 签约日期

Summary:

2933499090. other compounds containing in the structure a quinoline or isoquinoline ring-system (whether or not hydrogenated), not further fused. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

4-乙氧基喹啉(13720-91-7)相关文献

  • 1. Alkylation of quinolines with trialkyl phosphates. Part 2. Mechanistic studies
    Judit Frank,Zoltán Mészáros,Tamás K?mives,Attila F. Márton,Ferenc Dutka J. Chem. Soc. Perkin Trans. 2 1980 401
  • 2. Reactivity of 2,2-diphenyl-1,2-dihydro-4-ethoxyquinolin-1-yloxyl towards oxygen- and carbon-centred radicals
    Patricia Carloni,Elisabetta Damiani,Marco Scattolini,Pierluigi Stipa,Lucedio Greci J. Chem. Soc. Perkin Trans. 2 2000 447
  • 3. 231. Synthetic antimalarials. Part XLVI. Some 4-dialkylaminoalkylaminoquinoline derivatives
    Justus K. Landquist J. Chem. Soc. 1951 1038
  • 4. 167. Synthetic antimalarials. Part XVII. Some aminoalkylaminoquinoline derivatives
    F. H. S. Curd,C. G. Raison,F. L. Rose J. Chem. Soc. 1947 899
  • 5. Cyclic amidines. Part III. 2-Acylamino-4-alkoxyquinolines
    R. Hardman,M. W. Partridge J. Chem. Soc. 1955 510
  • 6. 101. Strychnine and brucine. Part XVIII. Final stages of the degradation of dinitrostrychol and an account of some nitrohydroxyquinoline derivatives
    Kottiazath Narayana Menon,Robert Robinson J. Chem. Soc. 1932 780
  • 7. 120. Cyclic amidines. Part VI. 5- and 7-Substituted 2-amino-4-hydroxyquinolines
    R. Hardman,M. W. Partridge J. Chem. Soc. 1958 614
  • 8. Formula index
    J. Chem. Soc. 1932 3054
  • 9. Organic chemistry
    J. Chem. Soc. Abstr. 1906 90 A549
  • 10. Remarkable orientational effects in the displacement of the fluorine from heptafluoro-isoquinoline and -quinoline towards sulfur nucleophiles. Further reactions with oxygen nucleophiles
    Gerald M. Brooke,Richard D. Chambers,Christopher J. Drury,Michael J. Bower J. Chem. Soc. Perkin Trans. 1 1993 2201