| Weight | 156.568 g/mol |
|---|---|
| Formula | C7H5ClO2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
5-Chlorosalicylaldehyde (635-93-8)
5-chloro-salicylaldehyde
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- Synthesis and antimicrobial activities of Schiff bases derived from 5-chloro-salicylaldehyde. (European Journal of Medicinal Chemistry, 2007)
- Sensitive and selective fluorescence determination of trace hydrazine in aqueous solution utilizing 5-chlorosalicylaldehyde (Analytica Chimica Acta, 2008)
- Synthesis and characterization of new addition compounds of bis(substituted-salicylaldehydo) cobalt(II) with 2,2-bipyridine (bipy). Crystal and molecular structures of [CoII(3-methoxy-salicylaldehyde)2(bipy)] CH3OH (1) and [CoII(bipy)3]Br2 0.5(5-chloro-salicylaldehydeH) 1.5CH3OH (5) (Polyhedron, 2007)
- Synthesis, structural characterization, and anti-ulcerogenic activity of schiff base ligands derived from tryptamine and 5-chloro, 5-nitro, 3,5-ditertiarybutyl salicylaldehyde and their nickel(II), copper(II), and Zinc(II) complexes (Polyhedron, 2009)
- In vitro effect of 1-acyl-4-alkyl-(or aryl)-thiosemicarbazides 1-(5-cholrosalicylidine)-4-alkyl-(or aryl)-thiosemicarbazones and some hydrazones of 5-chlorosalicylaldehyde against pathogenic bacteria including Mycobacterium tuberculosis (H37Rv). (Indian Journal of Experimental Biology, 1968)
- 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)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 5-chloro-salicylaldehyde
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SMILESC1=CC(=C(C=C1Cl)C=O)O
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InChIKeyFUGKCSRLAQKUHG-UHFFFAOYSA-N
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5-Chlorosalicylaldehyde
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