CAS 6954-48-9
:6-Bromo-1,2-naphthoquinone
Description:
6-Bromo-1,2-naphthoquinone is an organic compound characterized by its structure, which features a naphthoquinone core with a bromine substituent at the 6-position. This compound is typically a yellow to orange solid, exhibiting a range of chemical properties due to the presence of both the quinone and bromine functional groups. It is known for its reactivity, particularly in electrophilic substitution reactions, and can participate in various organic transformations, including reduction and nucleophilic addition. The presence of the bromine atom enhances its electrophilic character, making it a useful intermediate in synthetic organic chemistry. Additionally, 6-bromo-1,2-naphthoquinone may exhibit biological activity, which has been explored in various studies, potentially contributing to its applications in pharmaceuticals and agrochemicals. Its solubility varies depending on the solvent, and it is generally handled with care due to its potential toxicity and reactivity. As with many quinones, it may also display interesting photochemical properties.
Formula:C10H5BrO2
InChI:InChI=1S/C10H5BrO2/c11-7-2-3-8-6(5-7)1-4-9(12)10(8)13/h1-5H
InChI key:InChIKey=MXWZRRPNVLCHMY-UHFFFAOYSA-N
SMILES:O=C1C=2C(=CC(Br)=CC2)C=CC1=O
Synonyms:- 1,2-Naphthalenedione, 6-Bromo-
- 1,2-Naphthoquinone, 6-bromo-
- 6-Bromo-1,2-naphthalenedione
- 6-Bromo-1,2-naphthoquinone
- Bonafton
- Bonaphthon
- Bonaphthone
- NSC 37564
- Ua 13082
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