2,3-Dibromo-1,4-naphthoquinone - CAS 13243-65-7

Catalog:	BB007591
Product Name:	2,3-Dibromo-1,4-naphthoquinone
CAS:	13243-65-7
Synonyms:	2,3-dibromonaphthalene-1,4-dione

Technical Data

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Computed Properties

IUPAC Name:	2,3-dibromonaphthalene-1,4-dione
Description:	2,3-Dibromo-1,4-naphthoquinone (CAS# 13243-65-7 ) is a useful research chemical.
Molecular Weight:	315.95
Molecular Formula:	C10H4Br2O2
Canonical SMILES:	C1=CC=C2C(=C1)C(=O)C(=C(C2=O)Br)Br
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
Boiling Point:	338.6 °C at 760 mmHg
Melting Point:	218-222 °C(lit.)
Purity:	95 %
Density:	2.145 g/cm³
Appearance:	Yellow to orange powder or crystals
MDL:	MFCD00019526
LogP:	3.06700

Publication Number	Title	Priority Date
CN-113292503-A	Preparation method of 2-bromo-3-aminonaphthoquinone compound	20210522
JP-2021006572-A	Aminonaphthoquinone compounds, and pharmaceutical compositions for blocking the ubiquitination-proteasome system in disease	20201005
WO-2021110385-A1	Electrolyte composition with fluorinated acyclic carbonate and fluorinated cyclic carbonate	20191203
WO-2021040014-A1	Polymeric material, production method therefor, and polymeric material composition	20190830
KR-20200059648-A	Electrolyte composition having high energy density property and electrochemical cell including the same	20181121

PMID	Publication Date	Title	Journal
22704656	20120715	Analogs of N'-hydroxy-N-(4H,5H-naphtho[1,2-d]thiazol-2-yl)methanimidamide inhibit Mycobacterium tuberculosis methionine aminopeptidases	Bioorganic & medicinal chemistry
21989734	20120201	Synthesis and antioxidant evaluation of some new pyrazolopyridine derivatives	Archiv der Pharmazie
23037165	20120101	Leishmanicidal activity of two naphthoquinones against Leishmania donovani	Biological & pharmaceutical bulletin
22114475	20110101	Cytotoxicity of naphthoquinones and their capacity to generate reactive oxygen species is quenched when conjugated with gold nanoparticles	International journal of nanomedicine
18309277	20080201	Acaricidal activity and function of mite indicator using plumbagin and its derivatives isolated from Diospyros kaki Thunb. roots (Ebenaceae)	Journal of microbiology and biotechnology

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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

Complexity:	301
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	1
Defined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Exact Mass:	315.85576
Formal Charge:	0
Heavy Atom Count:	14
Hydrogen Bond Acceptor Count:	2
Hydrogen Bond Donor Count:	0
Isotope Atom Count:	0
Monoisotopic Mass:	313.85780
Rotatable Bond Count:	0
Topological Polar Surface Area:	34.1 Å²
Undefined Atom Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0
XLogP3:	2.8