| Weight | 232.666 g/mol |
|---|---|
| Formula | C13H9ClO2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 2 |
5-Chloro-2-hydroxybenzophenone (85-19-8)
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- Nitrogen-oxygen donor macrocyclic ligands. 3. Cobalt(II) complexes of cyclic diimine ligands derived from salicylaldehyde and 5-chloro-2-hydroxybenzophenone. X-ray structure determination of cis-dithiocyanato(5,6:14,15-dibenzo-1,4-dioxa-8,12-diazacyclopentadecane-7,12-diene)cobalt(II) (Inorganic Chemistry, 1977)
- On the chiroptical properties of ketimine structures derived from 5-chloro-2-hydroxybenzophenone (Tetrahedron, 1975)
- Reaction of 5-Chloro-2-hydroxybenzophenone and Phosphorus Pentachloride. Structural Studies1 (Journal of Organic Chemistry, 1966)
- Reactions of chlorosilanes and 5-chloro-2-hydroxybenzophenone (Journal of Organic Chemistry, 1969)
- 5-Chloro-2-hydroxybenzophenone, featuring O-H...O, C-H...O, C-H... and - interactions (Acta Crystallographica Section C-crystal Structure Communications, 2003)
- Correction. Reaction of 5-Chloro-2-hydroxybenzophenone and Phosphorus Pentachloride. Structural Studies. (Journal of Organic Chemistry, 1967)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C(C=C1)C(=O)C2=C(C=CC(=C2)Cl)O
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InChIKeyOMWSZDODENFLSV-UHFFFAOYSA-N
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