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254681

Sigma-Aldrich

3,5-Dichlorosalicylic acid

97%

Synonyme(s) :

3,5-Dichloro-2-hydroxybenzoic acid

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About This Item

Formule linéaire :
Cl2C6H2(OH)CO2H
Numéro CAS:
320-72-9
Poids moléculaire :
207.01
Numéro CE :
206-281-8
Numéro MDL:
MFCD00002442
Code UNSPSC :
12352100
ID de substance PubChem :
24855401
Nomenclature NACRES :
NA.22

Pureté

97%

Pf

220-222 °C (lit.)

Chaîne 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)

Clé InChI

CNJGWCQEGROXEE-UHFFFAOYSA-N

Catégories apparentées

Description générale

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.

Pictogrammes

Exclamation mark
GHS07

Mention d'avertissement

Warning

Mentions de danger

H302,H315,H319,H335

Classification des risques

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Organes cibles

Respiratory system

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Gloves

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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
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)
Armelle Tchoumi Neree et al.
Scientific reports, 10(1), 21563-21563 (2020-12-11)
Excess of histamine in gut lumen generates a pronounced gastrointestinal discomfort, which may include diarrhea and peristalsis dysfunctions. Deleterious effects of histamine can be alleviated with antihistamine drugs targeting histamine receptors. However, many antihistamine agents come with various undesirable side
Zhenxuan Zhang et al.
Water research, 170, 115283-115283 (2019-11-19)
Halogenated aromatic disinfection byproducts (DBPs) are a new group of emerging DBPs identified recently. They have been detected in disinfected drinking water, wastewater effluents, recreational water and oil/gas produced water, at concentrations of ng/L to μg/L in general. Previously studies
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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