Home Other Building Blocks N1-(7-Chloroquinolin-4-yl)ethane-1,2-diamine

N1-(7-Chloroquinolin-4-yl)ethane-1,2-diamine

CAS No.:
5407-57-8
Catalog Number:
AG00DGUR
Molecular Formula:
C11H12ClN3
Molecular Weight:
221.6861
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
250mg
95%
1 week
United States
$281
- +
1g
95%
1 week
United States
$645
- +
Product Description
Catalog Number:
AG00DGUR
Chemical Name:
N1-(7-Chloroquinolin-4-yl)ethane-1,2-diamine
CAS Number:
5407-57-8
Molecular Formula:
C11H12ClN3
Molecular Weight:
221.6861
MDL Number:
MFCD02179802
IUPAC Name:
N'-(7-chloroquinolin-4-yl)ethane-1,2-diamine
InChI:
InChI=1S/C11H12ClN3/c12-8-1-2-9-10(15-6-4-13)3-5-14-11(9)7-8/h1-3,5,7H,4,6,13H2,(H,14,15)
InChI Key:
XBDASFGJHWAFFE-UHFFFAOYSA-N
SMILES:
NCCNc1ccnc2c1ccc(c2)Cl
NSC Number:
5447
Properties
Complexity:
200  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
221.072g/mol
Formal Charge:
0
Heavy Atom Count:
15  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
221.688g/mol
Monoisotopic Mass:
221.072g/mol
Rotatable Bond Count:
3  
Topological Polar Surface Area:
50.9A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2  
Literature
Title Journal
Synthesis and evaluation of hybrid drugs for a potential HIV/AIDS-malaria combination therapy. Bioorganic & medicinal chemistry 20120901
Effects of highly active novel artemisinin-chloroquinoline hybrid compounds on β-hematin formation, parasite morphology and endocytosis in Plasmodium falciparum. Biochemical pharmacology 20110801
Antiplasmodial and antitumor activity of dihydroartemisinin analogs derived via the aza-Michael addition reaction. Bioorganic & medicinal chemistry letters 20110515
Synthesis and antimalarial activities of rhenium bioorganometallics based on the 4-aminoquinoline structure. Bioorganic & medicinal chemistry 20101115
Synthesis and anti-prion activity evaluation of aminoquinoline analogues. European journal of medicinal chemistry 20101101
Design, synthesis, and in vitro antiprotozoal, antimycobacterial activities of N-{2-[(7-chloroquinolin-4-yl)amino]ethyl}ureas. Bioorganic & medicinal chemistry 20100901
Synthesis and in vitro antitubercular activity of a series of quinoline derivatives. Bioorganic & medicinal chemistry 20090215
Antimalarial dual drugs based on potent inhibitors of glutathione reductase from Plasmodium falciparum. Journal of medicinal chemistry 20080313
Properties