4-Aminoquinoline - CAS 578-68-7
Catalog: |
BB029853 |
Product Name: |
4-Aminoquinoline |
CAS: |
578-68-7 |
Synonyms: |
4-quinolinamine; quinolin-4-amine |
IUPAC Name: | quinolin-4-amine |
Description: | 4-Aminoquinoline (CAS# 578-68-7) is a useful research chemical. |
Molecular Weight: | 144.17 |
Molecular Formula: | C9H8N2 |
Canonical SMILES: | C1=CC=C2C(=C1)C(=CC=N2)N |
InChI: | InChI=1S/C9H8N2/c10-8-5-6-11-9-4-2-1-3-7(8)9/h1-6H,(H2,10,11) |
InChI Key: | FQYRLEXKXQRZDH-UHFFFAOYSA-N |
Boiling Point: | 332.3 °C at 760 mmHg |
Density: | 1.21 g/cm3 |
MDL: | MFCD00463448 |
LogP: | 2.39820 |
GHS Hazard Statement: | H302 (93.02%): Harmful if swallowed [Warning Acute toxicity, oral] |
Precautionary Statement: | P264, P270, P280, P301+P312, P302+P352, P305+P351+P338, P321, P330, P332+P313, P337+P313, P362, and P501 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
CN-113057946-A | Dihydroartemisinin piperaquine tablet and preparation method thereof | 20210330 |
CN-113024513-A | Novel androgen receptor degradation agent, preparation method and medical application | 20210322 |
CN-113461669-A | Novel androgen receptor degradation agent, preparation method and medical application | 20210322 |
CN-112608327-A | Furanoquinoline derivative, preparation method and application thereof | 20210128 |
CN-112409254-A | Preparation method of naphthoquine phosphate | 20201208 |
PMID | Publication Date | Title | Journal |
31260299 | 20190725 | Discovery of 4-Aminoquinoline-3-carboxamide Derivatives as Potent Reversible Bruton's Tyrosine Kinase Inhibitors for the Treatment of Rheumatoid Arthritis | Journal of medicinal chemistry |
28869400 | 20171001 | Azide-alkyne cycloaddition en route to 4-aminoquinoline-ferrocenylchalcone conjugates: synthesis and anti-TB evaluation | Future medicinal chemistry |
28274627 | 20170415 | Three-component, one-pot synthesis of anthranilamide Schiff bases bearing 4-aminoquinoline moiety as Mycobacterium tuberculosis gyrase inhibitors | Bioorganic & medicinal chemistry letters |
27075024 | 20160501 | Naphthoquine: An Emerging Candidate for Artemisinin Combination Therapy | Drugs |
25525263 | 20150306 | New insights on the mechanism of quinoline-based DNA Methyltransferase inhibitors | The Journal of biological chemistry |
Complexity: | 136 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 144.068748264 |
Formal Charge: | 0 |
Heavy Atom Count: | 11 |
Hydrogen Bond Acceptor Count: | 2 |
Hydrogen Bond Donor Count: | 1 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 144.068748264 |
Rotatable Bond Count: | 0 |
Topological Polar Surface Area: | 38.9 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 1.6 |
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Related Functional Groups
Amines and Anilines
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