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 |
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 |
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 |
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 |
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 |
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