Cas no 13720-91-7 (4-Ethoxyquinoline)
4-Ethoxyquinoline structure
Product Name:4-Ethoxyquinoline
CAS No:13720-91-7
MF:C11H11NO
MW:173.211142778397
CID:212883
PubChem ID:139567
Update Time:2025-04-19
4-Ethoxyquinoline Chemical and Physical Properties
Names and Identifiers
-
- 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
-
- Inchi： 1S/C11H11NO/c1-2-13-11-7-8-12-10-6-4-3-5-9(10)11/h3-8H,2H2,1H3
- InChI Key： NBAWYUCPNKZTER-UHFFFAOYSA-N
- SMILES： O(CC)C1C=CN=C2C=CC=CC=12
Computed Properties
- Exact Mass: 173.08400
- Monoisotopic Mass: 173.084063974g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 13
- Rotatable Bond Count: 2
- Complexity: 160
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 1.3
- Topological Polar Surface Area: 22.1?2
Experimental Properties
- PSA: 22.12000
- LogP: 2.63350
4-Ethoxyquinoline Customs Data
- HS CODE：2933499090
- Customs Data：
China Customs Code:
2933499090Overview:
2933499090. Other compounds containing quinoline or isoquinoline ring system [but not further fused]. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%
Declaration elements:
Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date
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-Ethoxyquinoline Related Literature
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1. Alkylation of quinolines with trialkyl phosphates. Part 2. Mechanistic studiesJudit Frank,Zoltán Mészáros,Tamás K?mives,Attila F. Márton,Ferenc Dutka J. Chem. Soc. Perkin Trans. 2 1980 401
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2. Reactivity of 2,2-diphenyl-1,2-dihydro-4-ethoxyquinolin-1-yloxyl towards oxygen- and carbon-centred radicalsPatricia Carloni,Elisabetta Damiani,Marco Scattolini,Pierluigi Stipa,Lucedio Greci J. Chem. Soc. Perkin Trans. 2 2000 447
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3. 231. Synthetic antimalarials. Part XLVI. Some 4-dialkylaminoalkylaminoquinoline derivativesJustus K. Landquist J. Chem. Soc. 1951 1038
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4. 167. Synthetic antimalarials. Part XVII. Some aminoalkylaminoquinoline derivativesF. H. S. Curd,C. G. Raison,F. L. Rose J. Chem. Soc. 1947 899
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5. Cyclic amidines. Part III. 2-Acylamino-4-alkoxyquinolinesR. Hardman,M. W. Partridge J. Chem. Soc. 1955 510
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