Cas no 23432-42-0 (6-Nitroquinolin-4-ol)
6-Nitroquinolin-4-ol structure
Product Name:6-Nitroquinolin-4-ol
CAS No:23432-42-0
MF:C9H6N2O3
MW:190.15554189682
MDL:MFCD00024012
CID:276394
PubChem ID:254285
Update Time:2025-04-19
6-Nitroquinolin-4-ol Chemical and Physical Properties
Names and Identifiers
-
- 6-Nitroquinolin-4-ol
- 4-HYDROXY-6-NITROQUINOLINE
- 4-Quinolinol, 6-nitro-
- 6-nitro-4-Quinolinol
- 4-Hydroxy-6-nitrochinolin
- 6-Nitro-chinolin-4-ol
- 6-nitro-quinolin-4-ol
- SMR000185133
- SCHEMBL537862
- NSC78445
- 6-nitroquinoline-4[1h]-one
- NSC-78445
- FT-0600249
- CS-0102491
- CS-16703
- AKOS006271760
- Oprea1_398077
- DTXSID70946087
- EN300-320962
- Y14688
- J-515507
- MLS000573199
- AKOS016001677
- Cambridge id 5266729
- SY033819
- HMS2734K10
- SB68170
- CHEMBL1077560
- MFCD00024012
- AMY13983
- 6-nitro-4(1H)-quinolinone
- A26222
- 23432-42-0
- AC-9592
- A878893
- 6-nitro-4-hydroxyquinoline
- 6-nitro-1H-quinolin-4-one
- SB67625
- 6-nitroquinolin-4(1H)-one
- DB-008407
-
- MDL： MFCD00024012
- Inchi： 1S/C9H6N2O3/c12-9-3-4-10-8-2-1-6(11(13)14)5-7(8)9/h1-5H,(H,10,12)
- InChI Key： MGCGVNRWZOHFTO-UHFFFAOYSA-N
- SMILES： O=C1C=CNC2C=CC(=CC=21)[N+](=O)[O-]
Computed Properties
- Exact Mass: 190.03800
- Monoisotopic Mass: 190.038
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 14
- Rotatable Bond Count: 1
- Complexity: 295
- 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: 0.4
- Topological Polar Surface Area: 74.9A^2
Experimental Properties
- Density: 1.419
- Boiling Point: 362.6 ℃ at 760 mmHg
- Flash Point: 173.1°C
- Refractive Index: 1.636
- PSA: 78.94000
- LogP: 2.37180
6-Nitroquinolin-4-ol 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%
6-Nitroquinolin-4-ol Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Chemenu | CM144696-5g |
6-Nitroquinolin-4-ol |
23432-42-0 | 95% | 5g |
$489 | 2021-08-05 | |
| Apollo Scientific | OR962452-1g |
4-Hydroxy-6-nitroquinoline |
23432-42-0 | 96% | 1g |
￡119.00 | 2025-02-21 | |
| Chemenu | CM144696-250mg |
6-Nitroquinolin-4-ol |
23432-42-0 | 95%+ | 250mg |
$183 | 2024-07-28 | |
| Chemenu | CM144696-1g |
6-Nitroquinolin-4-ol |
23432-42-0 | 95%+ | 1g |
$327 | 2024-07-28 | |
| Chemenu | CM144696-5g |
6-Nitroquinolin-4-ol |
23432-42-0 | 95%+ | 5g |
$721 | 2024-07-28 | |
| abcr | AB313204-250 mg |
4-Hydroxy-6-nitroquinoline; 95% |
23432-42-0 | 250mg |
€144.00 | 2023-04-26 | ||
| abcr | AB313204-1 g |
4-Hydroxy-6-nitroquinoline; 95% |
23432-42-0 | 1g |
€271.50 | 2023-04-26 | ||
| abcr | AB313204-5 g |
4-Hydroxy-6-nitroquinoline; 95% |
23432-42-0 | 5g |
€628.50 | 2023-04-26 | ||
| abcr | AB313204-10 g |
4-Hydroxy-6-nitroquinoline; 95% |
23432-42-0 | 10g |
€1062.00 | 2023-04-26 | ||
| eNovation Chemicals LLC | D548840-1g |
6-Nitroquinolin-4-ol |
23432-42-0 | 97% | 1g |
$518 | 2023-09-02 |
6-Nitroquinolin-4-ol Related Literature
-
1. Heteroaromatic reactivity. Part VI. Kinetics and products of the nitration of 4-hydroxyquinoline, 1-methyl-4-quinolone, 4-methoxyquinoline, and 4-hydroxycinnoline in sulphuric acidR. B. Moodie,J. R. Penton,K. Schofield J. Chem. Soc. B 1971 1493
-
2. 733. Ultra-violet absorption spectra of some derivatives of quinoline, quinazoline, and cinnolineJ. M. Hearn,R. A. Morton,J. C. E. Simpson J. Chem. Soc. 1951 3318
-
K. Elliott,E. Tittensor J. Chem. Soc. 1959 484
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