61292-08-8 Usage
Description
4-Methyl-2-phenyl-1,3-thiazole-5-carbohydrazide is a chemical compound belonging to the thiazole derivative class, featuring a carbohydrazide functional group. Its unique structure indicates potential bioactive properties and applications in medicinal chemistry. Thiazole derivatives are known for their diverse pharmacological activities, such as antimicrobial, antitumor, antifungal, antiviral, and anti-inflammatory effects. The presence of the carbohydrazide moiety in the compound further suggests its potential as a bioactive scaffold in drug design and development, making it a promising candidate for the discovery of novel therapeutic agents with significant pharmacological activities.
Uses
Used in Pharmaceutical Industry:
4-Methyl-2-phenyl-1,3-thiazole-5-carbohydrazide is used as a bioactive scaffold for drug design and development due to its potential to exhibit diverse pharmacological activities. Its structure and functional groups make it a promising candidate for the creation of novel therapeutic agents.
Used in Antimicrobial Applications:
4-Methyl-2-phenyl-1,3-thiazole-5-carbohydrazide is used as an antimicrobial agent for its potential to combat various microorganisms, including bacteria and fungi, due to the known antimicrobial properties of thiazole derivatives.
Used in Antitumor Applications:
4-Methyl-2-phenyl-1,3-thiazole-5-carbohydrazide is used as an antitumor agent for its potential to exhibit antitumor properties, which could be beneficial in the development of cancer treatments.
Used in Anti-inflammatory Applications:
4-Methyl-2-phenyl-1,3-thiazole-5-carbohydrazide is used as an anti-inflammatory agent for its potential to reduce inflammation, which could be useful in the treatment of various inflammatory conditions.
Used in Antiviral Applications:
4-Methyl-2-phenyl-1,3-thiazole-5-carbohydrazide is used as an antiviral agent for its potential to inhibit viral replication and activity, which could be applied in the development of treatments for viral infections.
Further research and exploration of 4-Methyl-2-phenyl-1,3-thiazole-5-carbohydrazide may lead to the discovery of additional applications and therapeutic agents with significant pharmacological activities across various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 61292-08-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,2,9 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 61292-08:
(7*6)+(6*1)+(5*2)+(4*9)+(3*2)+(2*0)+(1*8)=108
108 % 10 = 8
So 61292-08-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H11N3OS/c1-7-9(10(15)14-12)16-11(13-7)8-5-3-2-4-6-8/h2-6H,12H2,1H3,(H,14,15)
61292-08-8Relevant articles and documents
New thiazolyl-triazole Schiff bases: Synthesis and evaluation of the anti-Candida potential
Stana, Anca,Enache, Alexandra,Vodnar, Dan Cristian,Nastasǎ, Cristina,Benedec, Daniela,Ionu?, Ioana,Login, Cezar,Marc, Gabriel,Oniga, Ovidiu,Tiperciuc, Br?ndu?a
, (2016/12/03)
In the context of the dangerous phenomenon of fungal resistance to the available therapies, we present here the chemical synthesis of a new series of thiazolyl-triazole Schiff bases B1-B15, which were in vitro assessed for their anti-Candida potential. Co
