8-Aminoquinoline - CAS 578-66-5

Catalog:	BB029851
Product Name:	8-Aminoquinoline
CAS:	578-66-5
Synonyms:	quinolin-8-amine

Technical Data

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Computed Properties

IUPAC Name:	quinolin-8-amine
Description:	8-Aminoquinoline (CAS# 578-66-5) is a useful research chemical.
Molecular Weight:	144.17
Molecular Formula:	C9H8N2
Canonical SMILES:	C1=CC2=C(C(=C1)N)N=CC=C2
InChI:	InChI=1S/C9H8N2/c10-8-5-1-3-7-4-2-6-11-9(7)8/h1-6H,10H2
InChI Key:	WREVVZMUNPAPOV-UHFFFAOYSA-N
Boiling Point:	174 °C (26 mmHg)
Purity:	98.0%
Density:	1.21 g/cm³
Appearance:	Yellow solidified mass or fragments
MDL:	MFCD00006809
LogP:	2.39820
Vapor Pressure:	0.00055 [mmHg]

Publication Number	Title	Priority Date
CN-113498790-A	Functional group immobilized nano-silver material, and preparation method and application thereof	20210702
CN-113372369-A	Preparation method of 2-formyl-4-fluorobenzeneboronic acid pinacol ester	20210525
CN-113201006-A	Method for synthesizing acyl silicon substituted isoindole-1-ketone analogue through rhodium-catalyzed hydrocarbon activation reaction	20210520
CN-113214224-A	Preparation method of polysubstituted 3-methylene isoindolinone derivative	20210510
CN-113150192-A	Chiral helix-loaded aromatic amide type resin and preparation method and application thereof	20210430

PMID	Publication Date	Title	Journal
30650322	20190117	Single-Dose Tafenoquine to Prevent Relapse of Plasmodium vivax Malaria	The New England journal of medicine
27528800	20160101	Tafenoquine and its potential in the treatment and relapse prevention of Plasmodium vivax malaria: the evidence to date	Drug design, development and therapy
24366744	20140101	KAI407, a potent non-8-aminoquinoline compound that kills Plasmodium cynomolgi early dormant liver stage parasites in vitro	Antimicrobial agents and chemotherapy
22950851	20121005	Evaluation of electrophilic heteroaromatic substitution: synthesis of heteroaromatic-fused pyrimidine derivatives via sequential three-component heterocyclization	The Journal of organic chemistry
22922313	20121001	Mn(II) complexes with sulfonamides as ligands. DNA interaction studies and nuclease activity	Journal of inorganic biochemistry

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Related Functional Groups

Quinoline/Isoquinoline

[203506-30-3]
2-Amino-6-methoxy-3-methylquinoline
[91092-92-1]
3-Carbomethoxy-1,2,3,4-tetrahydroisoquinoline-1,4-dione
[1535306-28-5]
6-Fluoro-8-iodoquinolin-2(1H)-one
[312713-96-5]
7-Chloro-6-methyl-3a,4,5,9b-tetrahydro-3H-cyclopenta[c]quinoline-4-carboxylic acid
[19490-87-0]
7-Methoxy-2-methylquinoline
[1394843-51-6]
3-Hydroxy-1-methyl-6-nitroquinolin-2(1H)-one

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GHS Hazard Statement:	H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
Precautionary Statement:	P201, P202, P261, P264, P271, P280, P281, P302+P352, P304+P340, P305+P351+P338, P308+P313, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501
Signal Word:	Warning

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:	1.8