5-Chlorosalicylic acid
[CAS# 321-14-2]

Identification

• Classification: Chemical reagent >> Organic reagent >> Aromatic acid
• Name: 5-Chlorosalicylic acid
• Synonyms: 5-Chloro-2-hydroxybenzoic acid
• Molecular Formula: C₇H₅ClO₃
• Molecular Weight: 172.57
• CAS Registry Number: 321-14-2
• EC Number: 206-283-9
• SMILES: C1=CC(=C(C=C1Cl)C(=O)O)O

Properties

• Melting point: 171-176 ºC
• Water solubility: 1 g/L (20 ºC)
• Density: 1.5±0.1 g/cm³, Calc.^*
• Index of Refraction: 1.630, Calc.^*
• Boiling Point: 320.5±27.0 ºC (760 mmHg), Calc.^*
• Flash Point: 147.6±23.7 ºC, Calc.^*

Safety Data

• Hazard Symbols: GHS06;GHS07 Danger
• Hazard Statements: H301-H315-H319-H335
• Precautionary Statements: P261-P264-P264+P265-P270-P271-P273-P280-P301+P316-P302+P352-P304+P340-P305+P351+P338-P319-P321-P330-P332+P317-P337+P317-P362+P364-P391-P403+P233-P405-P501

Hazard Classification

Hazard	Class	Category Code	Hazard Statement
Acute toxicity	Acute Tox.	3	H301
Skin irritation	Skin Irrit.	2	H315
Eye irritation	Eye Irrit.	2	H319
Specific target organ toxicity - single exposure	STOT SE	3	H335
Eye irritation	Eye Irrit.	2A	H319

Discovory and Applicatios

5-Chlorosalicylic acid, a chlorinated derivative of salicylic acid, is an important compound in organic chemistry and pharmaceutical applications. Its discovery dates back to the early 20th century, when researchers began exploring the properties and reactions of salicylic acid and its derivatives. Salicylic acid itself was first isolated from willow bark and has a long history of use, particularly in the development of aspirin. The introduction of chlorine atoms into the salicylic acid structure produced 5-chlorosalicylic acid, which possesses unique chemical and biological properties.

The synthesis of 5-chlorosalicylic acid typically involves the chlorination of salicylic acid. Various methods have been developed to achieve this, including electrophilic aromatic substitution reactions, where chlorine is introduced at the 5-position of the aromatic ring. This modification not only enhances the compound's solubility in organic solvents but also imparts specific pharmacological activities.

5-Chlorosalicylic acid is primarily recognized for its role as a pharmaceutical intermediate. It has been used in the synthesis of various therapeutic agents, particularly in the field of anti-inflammatory and analgesic medications. Its structural similarity to salicylic acid allows it to exhibit similar biological activities, including anti-inflammatory properties. Researchers have also explored its potential as an antimicrobial agent, showcasing its efficacy against a range of bacterial and fungal strains.

In addition to its pharmaceutical applications, 5-chlorosalicylic acid serves as a versatile reagent in organic synthesis. It is utilized in the production of agrochemicals, dyes, and other fine chemicals. Its chlorinated nature enhances the compound's reactivity, making it a valuable building block in the synthesis of more complex molecules.

Moreover, 5-chlorosalicylic acid has been studied for its potential role in cancer research. Preliminary studies suggest that it may inhibit the growth of certain cancer cell lines, indicating a possible application in cancer therapy. These findings have prompted further investigation into its mechanism of action and potential therapeutic benefits.

In summary, 5-chlorosalicylic acid is a significant chemical compound with a rich history and diverse applications. Its discovery marked a notable advancement in organic chemistry, and its continued exploration in pharmaceuticals and agrochemicals highlights its importance in contemporary research and industry. The compound's unique properties and potential therapeutic applications make it a subject of ongoing scientific interest, paving the way for future discoveries and innovations.