254681
3,5-Dichlorosalicylic acid
97%
Sinónimos:
3,5-Dichloro-2-hydroxybenzoic acid
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About This Item
Fórmula lineal:
Cl2C6H2(OH)CO2H
Número de CAS:
Peso molecular:
207.01
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de la sustancia en PubChem:
NACRES:
NA.22
Productos recomendados
Nivel de calidad
Ensayo
97%
mp
220-222 °C (lit.)
grupo funcional
carboxylic acid
chloro
cadena SMILES
OC(=O)c1cc(Cl)cc(Cl)c1O
InChI
1S/C7H4Cl2O3/c8-3-1-4(7(11)12)6(10)5(9)2-3/h1-2,10H,(H,11,12)
Clave InChI
CNJGWCQEGROXEE-UHFFFAOYSA-N
Categorías relacionadas
Descripción general
3,5-Dichlorosalicylic acid is a bio-active drug and its interaction with a model transport protein bovine serum albumin has been investigated. It is a potential inhibitor of human 20α-hydroxysteroid dehydrogenase.
Palabra de señalización
Warning
Frases de peligro
Consejos de prudencia
Clasificaciones de peligro
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Órganos de actuación
Respiratory system
Código de clase de almacenamiento
11 - Combustible Solids
Clase de riesgo para el agua (WGK)
WGK 3
Punto de inflamabilidad (°F)
Not applicable
Punto de inflamabilidad (°C)
Not applicable
Equipo de protección personal
dust mask type N95 (US), Eyeshields, Gloves
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Bijan Kumar Paul et al.
Physical chemistry chemical physics : PCCP, 14(25), 8892-8902 (2012-02-07)
The present work demonstrates a detailed characterization of the interaction of a bio-active drug molecule 3,5-dichlorosalicyclic acid (3,5DCSA) with a model transport protein Bovine Serum Albumin (BSA). The drug molecule is a potential candidate exhibiting Excited-State Intramolecular Proton Transfer (ESIPT)
Vincenzo Carbone et al.
Archives of biochemistry and biophysics, 479(1), 82-87 (2008-09-11)
The structure of aldehyde reductase (ALR1) in ternary complex with the coenzyme NADPH and 3,5-dichlorosalicylic acid (DCL), a potent inhibitor of human 20alpha-hydroxysteroid dehydrogenase (AKR1C1), was determined at a resolution of 2.41A. The inhibitor formed a network of hydrogen bonds
Armelle Tchoumi Neree et al.
Scientific reports, 10(1), 21563-21563 (2020-12-11)
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Zhenxuan Zhang et al.
Water research, 170, 115283-115283 (2019-11-19)
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Shaoyang Hu et al.
Chemosphere, 228, 668-675 (2019-05-10)
As the first identified category of disinfection byproducts (DBPs), trihalomethanes (THMs) have received continuous attention. Previous studies have demonstrated that the transformation of aromatic halogenated DBPs during chlor (am)ination resulted in the formation of THMs, which may occur in both
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