Home Halogens 1,4-Naphthalenedione, 2,3-dibromo-

1,4-Naphthalenedione, 2,3-dibromo-

CAS No.:
13243-65-7
Catalog Number:
AG0010OQ
Molecular Formula:
C10H4Br2O2
Molecular Weight:
315.9456
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Product Description
Catalog Number:
AG0010OQ
Chemical Name:
1,4-Naphthalenedione, 2,3-dibromo-
CAS Number:
13243-65-7
Molecular Formula:
C10H4Br2O2
Molecular Weight:
315.9456
MDL Number:
MFCD00019526
IUPAC Name:
2,3-dibromonaphthalene-1,4-dione
InChI:
InChI=1S/C10H4Br2O2/c11-7-8(12)10(14)6-4-2-1-3-5(6)9(7)13/h1-4H
InChI Key:
PSMABVOYZJWFBV-UHFFFAOYSA-N
SMILES:
O=C1C(=C(Br)C(=O)c2c1cccc2)Br
EC Number:
236-223-7
Properties
Complexity:
301  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
315.856g/mol
Formal Charge:
0
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
315.948g/mol
Monoisotopic Mass:
313.858g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
34.1A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.8  
Literature
Title Journal
Analogs of N'-hydroxy-N-(4H,5H-naphtho[1,2-d]thiazol-2-yl)methanimidamide inhibit Mycobacterium tuberculosis methionine aminopeptidases. Bioorganic & medicinal chemistry 20120715
Synthesis and antioxidant evaluation of some new pyrazolopyridine derivatives. Archiv der Pharmazie 20120201
Leishmanicidal activity of two naphthoquinones against Leishmania donovani. Biological & pharmaceutical bulletin 20120101
Cytotoxicity of naphthoquinones and their capacity to generate reactive oxygen species is quenched when conjugated with gold nanoparticles. International journal of nanomedicine 20110101
Acaricidal activity and function of mite indicator using plumbagin and its derivatives isolated from Diospyros kaki Thunb. roots (Ebenaceae). Journal of microbiology and biotechnology 20080201
Properties