Weight | 172.567 g/mol |
---|---|
Formula | C7H5ClO3 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 2 |
Aromatic Rings | 1 |
Rotatable Bonds | 1 |
5-CHLOROSALICYLIC ACID (321-14-2)
5-chlorosalicylic acid, monosodium salt · 5-chlorosalicylate · 5-chlorosalicylic acid, copper salt
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- New Bacterial Pathway for 4- and 5-Chlorosalicylate Degradation via 4-Chlorocatechol and Maleylacetate in Pseudomonas sp. Strain MT1 (Journal of Bacteriology, 2003)
- Excited state proton transfer: A new feature in the fluorescence of methyl 5-chlorosalicylate and methyl 5-methoxysalicylate (Journal of Photochemistry, 1985)
- Deciphering the photophysics of 5-chlorosalicylic acid: evidence for excited-state intramolecular proton transfer. (Photochemical and Photobiological Sciences, 2010)
- Catabolism of 5-chlorosalicylate by a Bacillus isolated from the Mississippi River. (Applied and Environmental Microbiology, 1979)
- Induction of phenylalanine ammonia lyase activity and control of Sphaeropsis sapinea infection in Pinus radiata by 5-chlorosalicylic acid (Forest Pathology, 1998)
- Structural studies on complexes IV: Crystal structure of a 1:1 5Chlorosalicylic Acid and theophylline complex (Journal of Pharmaceutical Sciences, 1969)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 5-chlorosalicylic acid, monosodium salt
- 5-chlorosalicylate
- 5-chlorosalicylic acid, copper salt
-
SMILESC1=CC(=C(C=C1Cl)C(=O)O)O
-
InChIKeyNKBASRXWGAGQDP-UHFFFAOYSA-N
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Similar Compounds
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methyl 4-chloro-2-hydroxybenzoate
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