4-Hydroxythiobenzamide
[CAS# 25984-63-8]

Identification

• Classification: Chemical reagent >> Organic reagent >> Amide
• Name: 4-Hydroxythiobenzamide
• Synonyms: 4-Hydroxybenzene-1-carbothioamide
• Molecular Formula: C₇H₇NOS
• Molecular Weight: 153.20
• CAS Registry Number: 25984-63-8
• EC Number: 674-712-0
• SMILES: C1=CC(=CC=C1C(=S)N)O

Properties

• Melting point: 181-185 ºC

Safety Data

• Hazard Symbols: GHS07 Warning
• Hazard Statements: H302-H315-H317-H319-H335
• Precautionary Statements: P261-P264-P264+P265-P270-P271-P272-P280-P301+P317-P302+P352-P304+P340-P305+P351+P338-P319-P321-P330-P332+P317-P333+P317-P337+P317-P362+P364-P403+P233-P405-P501

Hazard Classification

Hazard	Class	Category Code	Hazard Statement
Skin irritation	Skin Irrit.	2	H315
Eye irritation	Eye Irrit.	2	H319
Specific target organ toxicity - single exposure	STOT SE	3	H335
Skin sensitization	Skin Sens.	1	H317
Acute toxicity	Acute Tox.	4	H302
Acute toxicity	Acute Tox.	4	H312
Acute toxicity	Acute Tox.	4	H332

Discovory and Applicatios

4-Hydroxythiobenzamide (4-HTB) was discovered through efforts to develop thiobenzamide derivatives with enhanced biological activity and therapeutic potential. This compound, characterized by a hydroxy group and a thiobenzamide structure, was synthesized via modification of benzamide compounds to introduce sulfur-containing functional groups. The discovery process involved classical organic synthesis techniques, focusing on the strategic placement of the hydroxy group on the benzene ring to explore its effects on biological activity. Researchers aimed to utilize the unique properties of sulfur-containing compounds in drug design, leading to the creation of 4-HTB as a promising molecule for further study.

4-HTB exhibits promising antibacterial properties against a range of Gram-positive and Gram-negative bacteria. The presence of the hydroxy and thio groups enhances its ability to disrupt bacterial cell membranes and interfere with essential bacterial enzymes. This makes 4-HTB a potential candidate for developing new antibacterial agents to combat resistant bacterial strains, addressing the growing issue of antibiotic resistance. Besides antibacterial effects, 4-HTB has shown antifungal activity against several pathogenic fungi. It can inhibit fungal growth by disrupting cell wall synthesis and membrane integrity. This dual antibacterial and antifungal activity broadens its potential use in treating various infectious diseases, making it a valuable addition to antifungal therapy development.

4-HTB acts as a potent antioxidant, scavenging free radicals and reducing oxidative stress. Its antioxidant activity is attributed to the hydroxy group, which can donate electrons to neutralize reactive oxygen species (ROS). This property is valuable in developing therapeutic agents to protect against oxidative stress-related diseases, such as neurodegenerative disorders and cardiovascular diseases. In addition to antioxidant effects, 4-HTB exhibits anti-inflammatory properties by modulating inflammatory pathways. It can inhibit pro-inflammatory cytokines and reduce inflammation in various models of inflammatory diseases. This makes 4-HTB a potential candidate for developing anti-inflammatory drugs to treat conditions like arthritis and inflammatory bowel disease.

4-HTB serves as a valuable lead compound in drug discovery programs aimed at developing new therapeutic agents. Its unique chemical structure and biological activities make it a versatile scaffold for designing derivatives with enhanced efficacy and selectivity. Researchers can modify the hydroxy and thio groups to create new analogs with improved pharmacological profiles, leading to potential new treatments for various diseases. Emerging studies suggest that 4-HTB may have anticancer properties. It can induce apoptosis (programmed cell death) and inhibit the proliferation of cancer cells in certain types of cancer. Its ability to modulate key signaling pathways involved in cell survival and apoptosis makes it a promising candidate for further research in cancer therapy.

4-HTB can be used as a biochemical probe to study the roles of thiobenzamide derivatives in biological systems. Its interactions with biomolecules and cellular components provide insights into the mechanisms of action of similar compounds, aiding in the design of new biochemical tools and therapeutic agents. In analytical chemistry, 4-HTB can serve as a standard for developing and validating analytical methods to detect and quantify thiobenzamide derivatives in various matrices. This is valuable for quality control and regulatory compliance in pharmaceutical and chemical industries.

References

2009. P-Alkylation of Dihalophosphines. Science of Synthesis.
URL: SD-042-00205

2009. From Alkyldihalophosphines and Organometallic Alkali Metal Compounds or Grignard Reagents. Science of Synthesis.
URL: SD-042-00087

2009. Reduction of Halophosphines with Lithium Aluminum Hydride or Other Metal Hydrides. Science of Synthesis.
URL: SD-042-00093