| Weight | 192.601 g/mol |
|---|---|
| Formula | C10H5ClO2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
2-Chloro-1,4-naphthoquinone (1010-60-2)
chloro-K3
Score:
#53 in Medicinal chemistry
,
#2894 in Biochemistry
,
#7076 in Chemistry
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- Potential antimalarial agents. Derivatives of 2-chloro-1,4-naphthoquinone. (Journal of Medicinal Chemistry, 1969)
- A new general regiocontrolled synthesis of anthracyclinones using cycloaddition of homophthalic anhydrides to 2-chloro-6-oxo-5,6,7,8-tetrahydro-1,4-naphthoquinone 1,2-ethanediyl acetal (Journal of Organic Chemistry, 1982)
- Synthesis and antiplatelet, antiinflammatory, and antiallergic activities of 2-substituted 3-chloro-1,4-naphthoquinone derivatives (Bioorganic & Medicinal Chemistry, 1997)
- Antithrombotic and antiplatelet activities of 2-chloro-3-[4-(ethylcarboxy)-phenyl]-amino-1,4-naphthoquinone (NQ12), a newly synthesized 1,4-naphthoquinone derivative. (Biochemical Pharmacology, 2000)
- Antiplatelet Activity of J78 (2-Chloro-3-[2-bromo, 4-fluoro-phenyl]-amino-8-hydroxy-1,4-naphthoquinone), an Antithrombotic Agent, Is Mediated by Thromboxane (TX) A2 Receptor Blockade with TXA2 Synthase Inhibition and Suppression of Cytosolic Ca2+ Mobilization (Journal of Pharmacology and Experimental Therapeutics, 2004)
- Synthetic schistosomicides. XIV. 1,4-Naphthoquinone mono(O-acyloximes), 4-amino-1,2-naphthoquinones, 2-amino-3-chloro-1,4-naphthoquinones, and other naphthoquinones (Journal of Medicinal Chemistry, 1970)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - chloro-K3
-
SMILESC1=CC=C2C(=C1)C(=O)C=C(C2=O)Cl
-
InChIKeyCCTJHVLTAJTPBV-UHFFFAOYSA-N
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