H47003
5-Hydroxy-1,4-naphthoquinone
97%
Synonym(s):
Juglone
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About This Item
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Quality Level
Assay
97%
mp
161-163 °C (lit.)
SMILES string
Oc1cccc2C(=O)C=CC(=O)c12
InChI
1S/C10H6O3/c11-7-4-5-9(13)10-6(7)2-1-3-8(10)12/h1-5,12H
InChI key
KQPYUDDGWXQXHS-UHFFFAOYSA-N
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Application
5-Hydroxy-1,4-naphthoquinone (juglone) can be used as a starting material for the synthesis of:
Juglone can also be used as a dienophile in the Diels–Alder reaction for the synthesis of variety of C-aryl glycosides.
- Trypanocidal drugs.
- Tacrine-naphthoquinone hybrids with potential application in the treatment of Alzheimer′s disease.
- Juglone-based electroactive polymer, poly(5-hydroxy-1,4-naphthoquinone-co-5-hydroxy-3-thioacetic acid-1,4-naphthoquinone), for the electrochemical detection of DNA hybridization.
- Ent-nocardione A, naturally-occurring tyrosine phosphatase inhibitor.
Juglone can also be used as a dienophile in the Diels–Alder reaction for the synthesis of variety of C-aryl glycosides.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 3 Oral
Storage Class Code
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Application of an Enyne Metathesis/Diels-Alder Cycloaddition Sequence: A New Versatile Approach to the Syntheses of C-Aryl Glycosides and Spiro-C-Aryl Glycosides.
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Journal of Electroanalytical Chemistry, 577(1), 155-165 (2005)
Formal Radical Cyclization onto Benzene Rings: A General Method and Its Use in the Synthesis of ent-Nocardione A.
The Journal of Organic Chemistry, 69(10), 3282-3293 (2004)
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