357782
2,3,5-Trichlorobenzoic acid
97%
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About This Item
Formula condensata:
Cl3C6H2CO2H
Numero CAS:
Peso molecolare:
225.46
Beilstein:
2097064
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
Livello qualitativo
Saggio
97%
Forma fisica
solid
Punto di fusione
166-167 °C (lit.)
Gruppo funzionale
carboxylic acid
chloro
Stringa SMILE
OC(=O)c1cc(Cl)cc(Cl)c1Cl
InChI
1S/C7H3Cl3O2/c8-3-1-4(7(11)12)6(10)5(9)2-3/h1-2H,(H,11,12)
CGFDSIZRJWMQPP-UHFFFAOYSA-N
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Categorie correlate
Avvertenze
Warning
Indicazioni di pericolo
Consigli di prudenza
Classi di pericolo
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Organi bersaglio
Respiratory system
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
dust mask type N95 (US), Eyeshields, Gloves
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Rearrangement of Halotropones. Chloride Exchange in Tribromotropolone.
Doering WE and Knox LH.
Journal of the American Chemical Society, 74(22), 5683-5687 (1952)
Effects of temperature on biological degradation of phenols, benzoates and phthalates under methanogenic conditions.
Leven L and Schnurer A.
International Biodeterioration & Biodegradation, 55(2), 153-160 (2005)
Fatima El-Athman et al.
Environmental science and pollution research international, 26(31), 32636-32644 (2019-10-22)
Triiodinated benzoic acid derivatives are widely used as contrast media for medical examinations and are found at high concentrations in urban aquatic environments. During bank filtration, deiodination of iodinated contrast media has been observed under anoxic/anaerobic conditions. While several bacterial
Meng Qi et al.
Analytical and bioanalytical chemistry, 412(25), 6995-7006 (2020-08-02)
Dicamba herbicide is increasingly used in the world, in particular' with the widespread cultivation of genetically modified dicamba-resistant crops. However, the drift problem in the field has caused phytotoxicity against naive, sensitive crops, raising legal concerns. Thus, it is particularly
Prakash Karegoudar et al.
European journal of medicinal chemistry, 43(4), 808-815 (2007-09-07)
The reaction of 2,3,5-trichlorobenzoic acid hydrazide with carbon disulfide and potassium hydroxide followed by treatment with hydrazine hydrate afforded 3-(2,3,5-trichlorophenyl)-4-amino-1,2,4-triazole-5-thione (6). Alternatively, this triazole was also synthesized by fusing 2,3,5-trichlorobenzoic acid with thiocarbohydrazide. Condensation of (6) with various aromatic carboxylic
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