2-Bromo-1,4-naphthoquinone - CAS 2065-37-4
Catalog: |
BB016131 |
Product Name: |
2-Bromo-1,4-naphthoquinone |
CAS: |
2065-37-4 |
Synonyms: |
2-bromonaphthalene-1,4-dione |
IUPAC Name: | 2-bromonaphthalene-1,4-dione |
Description: | 2-Bromo-1,4-naphthoquinone (CAS# 2065-37-4) is a structural analog of Vitamin K3 (V676130) and has been used in cancer research studies to increase H2O2 production in tumor cell lines. |
Molecular Weight: | 237.05 |
Molecular Formula: | C10H5BrO2 |
Canonical SMILES: | C1=CC=C2C(=C1)C(=O)C=C(C2=O)Br |
InChI: | InChI=1S/C10H5BrO2/c11-8-5-9(12)6-3-1-2-4-7(6)10(8)13/h1-5H |
InChI Key: | KJOHPBJYGGFYBJ-UHFFFAOYSA-N |
Boiling Point: | 324.2 °C at 760 mmHg |
Density: | 1.757 g/cm3 |
Appearance: | Light to dark yellow powder or crystals |
MDL: | MFCD00629301 |
LogP: | 2.34440 |
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-113461506-A | Preparation process of 2-bromo-1, 4-naphthoquinone | 20210623 |
CN-110183427-A | A kind of preparation method of the square ring element analog of the rhamnose of deoxidation containing 2- | 20190531 |
CN-110229170-A | A kind of preparation method of 5- azepine Marangucycline B | 20190531 |
CN-109748809-A | A method of synthesis 2- substituted-amino -1,4- naphthoquinone derivatives | 20190115 |
WO-2020028222-A1 | Compounds for the treatment of neurological or mitochondrial diseases | 20180729 |
PMID | Publication Date | Title | Journal |
29902415 | 20180801 | Synthesis of newly functionalized 1,4-naphthoquinone derivatives and their effects on wound healing in alloxan-induced diabetic mice | Chemico-biological interactions |
22584645 | 20120801 | 2-Bromo-1,4-naphthoquinone: a potentially improved substitute of menadione in Apatone™ therapy | Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas |
22483633 | 20120601 | On the search for potential anti-Trypanosoma cruzi drugs: synthesis and biological evaluation of 2-hydroxy-3-methylamino and 1,2,3-triazolic naphthoquinoidal compounds obtained by click chemistry reactions | European journal of medicinal chemistry |
22114475 | 20110101 | Cytotoxicity of naphthoquinones and their capacity to generate reactive oxygen species is quenched when conjugated with gold nanoparticles | International journal of nanomedicine |
18304897 | 20080315 | Bromide-sulfur interchange: ion chromatographic determination of total reduced thiol levels in plasma | Journal of chromatography. B, Analytical technologies in the biomedical and life sciences |
Complexity: | 293 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 235.94729 |
Formal Charge: | 0 |
Heavy Atom Count: | 13 |
Hydrogen Bond Acceptor Count: | 2 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 235.94729 |
Rotatable Bond Count: | 0 |
Topological Polar Surface Area: | 34.1 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 2.4 |
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