5-(p-Tolyl)-1,3,4-thiadiazol-2-amine
≥95%
Reagent
Code: #119860
CAS Number
26907-54-0
blur_circular Chemical Specifications
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Molecular Information
Weight
191.25 g/mol
Formula
C₉H₉N₃S
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Registry Numbers
MDL Number
MFCD00469688
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Physical Properties
Boiling Point
364.9°C at 760 mmHg
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Storage & Handling
Storage
2-8°C, protected from light, stored in an inert gas
description Product Description
This compound is primarily used in the field of medicinal chemistry due to its potential biological activities. It serves as a key intermediate in the synthesis of various pharmacologically active molecules, particularly those targeting antimicrobial, anticancer, and anti-inflammatory properties. Researchers explore its derivatives for developing new drugs, as the thiadiazole ring structure is known to enhance binding affinity and efficacy in drug-receptor interactions. Additionally, it finds applications in material science, where it is utilized in the development of organic semiconductors and optoelectronic devices due to its ability to form stable, conjugated systems. Its versatility makes it a valuable compound in both pharmaceutical and industrial research.
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5-(p-Tolyl)-1,3,4-thiadiazol-2-amine
This compound is primarily used in the field of medicinal chemistry due to its potential biological activities. It serves as a key intermediate in the synthesis of various pharmacologically active molecules, particularly those targeting antimicrobial, anticancer, and anti-inflammatory properties. Researchers explore its derivatives for developing new drugs, as the thiadiazole ring structure is known to enhance binding affinity and efficacy in drug-receptor interactions. Additionally, it finds applications in material science, where it is utilized in the development of organic semiconductors and optoelectronic devices due to its ability to form stable, conjugated systems. Its versatility makes it a valuable compound in both pharmaceutical and industrial research.
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