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5-(4-amino-2-hydroxyphenyl)-1,3,4-oxadiazole-2(5H)-thione is a chemical compound that belongs to the class of oxadiazole derivatives. It is characterized by its unique structure that includes an oxadiazole ring fused with a thiophene ring, along with an amino and hydroxyl group attached to the phenyl moiety. 5-(4-amino-2-hydroxyphenyl)-1,3,4-oxadiazole-2(5H)-thione is known for its potential medicinal properties and has been studied for its antimicrobial, antifungal, anti-inflammatory, and antioxidant effects.
Used in Pharmaceutical Industry:
5-(4-amino-2-hydroxyphenyl)-1,3,4-oxadiazole-2(5H)-thione is used as a pharmaceutical agent for its potential medicinal properties. 5-(4-amino-2-hydroxyphenyl)-1,3,4-oxadiazole-2(5H)-thione's antimicrobial, antifungal, and anti-inflammatory effects make it a promising candidate for the development of new drugs and treatments for various health conditions.
Used in Antimicrobial Applications:
In the field of antimicrobial research, 5-(4-amino-2-hydroxyphenyl)-1,3,4-oxadiazole-2(5H)-thione is used as an antimicrobial agent to combat various types of bacteria. Its ability to inhibit bacterial growth and disrupt their cellular functions makes it a valuable asset in the development of new antibiotics.
Used in Antifungal Applications:
5-(4-amino-2-hydroxyphenyl)-1,3,4-oxadiazole-2(5H)-thione is also used as an antifungal agent, targeting fungal infections and preventing their proliferation. Its effectiveness against fungi makes it a potential candidate for the development of new antifungal medications.
Used in Anti-inflammatory Applications:
In the realm of anti-inflammatory research, 5-(4-amino-2-hydroxyphenyl)-1,3,4-oxadiazole-2(5H)-thione is used as an agent to reduce inflammation and alleviate symptoms associated with inflammatory conditions. Its potential to modulate inflammatory responses could lead to the development of new treatments for various inflammatory diseases.
Used in Antioxidant Applications:
5-(4-amino-2-hydroxyphenyl)-1,3,4-oxadiazole-2(5H)-thione is used as an antioxidant, helping to neutralize harmful free radicals and protect cells from oxidative damage. Its antioxidant properties make it a promising candidate for the development of new therapies to combat oxidative stress-related conditions.
Research on 5-(4-amino-2-hydroxyphenyl)-1,3,4-oxadiazole-2(5H)-thione is ongoing, and its potential applications in the pharmaceutical industry continue to expand as new discoveries are made. Its diverse range of biological activities positions it as a versatile compound with the potential to contribute significantly to the development of new drugs and treatments for various health conditions.

3687-07-8

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3687-07-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3687-07-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,8 and 7 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3687-07:
(6*3)+(5*6)+(4*8)+(3*7)+(2*0)+(1*7)=108
108 % 10 = 8
So 3687-07-8 is a valid CAS Registry Number.

3687-07-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-amino-2-hydroxyphenyl)-2H-1,3,4-oxadiazole-5-thione

1.2 Other means of identification

Product number -
Other names 1,3,4-Oxadiazole-2(3H)-thione,5-(4-amino-2-hydroxyphenyl)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
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More Details:3687-07-8 SDS

3687-07-8Upstream product

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3687-07-8Relevant academic research and scientific papers

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