4-Chloroquinoline - CAS 611-35-8
Catalog: |
BB030967 |
Product Name: |
4-Chloroquinoline |
CAS: |
611-35-8 |
Synonyms: |
4-chloroquinoline |
IUPAC Name: | 4-chloroquinoline |
Description: | 4-Chloroquinoline (CAS# 611-35-8) is a useful research chemical. |
Molecular Weight: | 163.60 |
Molecular Formula: | C9H6ClN |
Canonical SMILES: | C1=CC=C2C(=C1)C(=CC=N2)Cl |
InChI: | InChI=1S/C9H6ClN/c10-8-5-6-11-9-4-2-1-3-7(8)9/h1-6H |
InChI Key: | KNDOFJFSHZCKGT-UHFFFAOYSA-N |
Boiling Point: | 260-261 °C |
Melting Point: | 28-31 °C |
Purity: | 98 % |
Density: | 1.25 g/cm3 |
Appearance: | Pale yellow low melting solid |
MDL: | MFCD00006773 |
LogP: | 2.88820 |
GHS Hazard Statement: | H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation] |
Precautionary Statement: | P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
CN-113214252-A | Synthesis method of 6-phenyl-7- (pyridine-2-yl) -7H-indolo [2,3-c ] quinoline compound | 20210528 |
CN-112961105-A | Alkylation method of nitrogen-containing heterocyclic compound | 20210128 |
CN-112390781-A | Diaryl substituted 1, 1-ethylene compound, preparation method and application | 20201118 |
CN-112390751-A | Toll-like receptor-7 small molecule inhibitor and preparation method thereof | 20201105 |
CN-111454252-A | Aromatic ring/aromatic heterocycle-triazole-methylene-TCP derivative and preparation method and application thereof | 20200513 |
PMID | Publication Date | Title | Journal |
18997944 | 20081121 | Chemoenzymatic synthesis of chiral 4,4'-bipyridyls and their metal-organic frameworks | Chemical communications (Cambridge, England) |
15902470 | 20050401 | Replacement of active-site residues of quinoline 2-oxidoreductase involved in substrate recognition and specificity | Current microbiology |
15762760 | 20050301 | Use of quinolinium salts in parallel synthesis for the preparation of 4-amino-2-alkyl-1,2,3,4-tetrahydroquinoline | Journal of combinatorial chemistry |
12946152 | 20030905 | Use of highly active palladium-phosphinous acid catalysts in Stille, Heck, amination, and thiation reactions of chloroquinolines | The Journal of organic chemistry |
Complexity: | 138 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 163.0188769 |
Formal Charge: | 0 |
Heavy Atom Count: | 11 |
Hydrogen Bond Acceptor Count: | 1 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 163.0188769 |
Rotatable Bond Count: | 0 |
Topological Polar Surface Area: | 12.9 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 1.6 |
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