| Weight | 204.656 g/mol |
|---|---|
| Formula | C12H9ClO |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 2 |
4-Chlorodiphenyl ether (7005-72-3)
4-CDE
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- New domino reaction for the selective synthesis of tetracyclic cinnolino[5,4,3-cde]cinnolines (Organic and Biomolecular Chemistry, 2009)
- A Novel Approach to the CDE Ring System of Pectenotoxin-4 Triggered by VO(acac)2-Induced Epoxy-Acetalization (Organic Letters, 2009)
- The reaction of sulfur with dilithio compounds. The syntheses and structures of phenanthro [1, 10cd]1,2dithiole and phenanthro[4,5cde] [1,2]dithiin (Heteroatom Chemistry, 1994)
- Polo-like kinase 4 transcription is activated via CRE and NRF1 elements, repressed by DREAM through CDE/CHR sites and deregulated by HPV E7 protein (Nucleic Acids Research, 2014)
- Synthesis of a New Azacyclizine, Indolizino[3,4,5,6-cde]quinoxaline (Heterocycles, 1980)
- Reactions of cyclic 1,3-diketones with hydrazine. Mechanism of cinnolino[5,4,3-cde]cinnoline formation. Unusual oxidation as a result of steric crowding (Journal of the American Chemical Society, 1968)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 4-CDE
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SMILESC1=CC=C(C=C1)OC2=CC=C(C=C2)Cl
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InChIKeyPGPNJCAMHOJTEF-UHFFFAOYSA-N
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4-Chlorodiphenyl ether
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