61292-08-8

Basic information

• Product Name: 4-METHYL-2-PHENYL-1,3-THIAZOLE-5-CARBOHYDRAZIDE
• Synonyms: 4-METHYL-2-PHENYL-1,3-THIAZOLE-5-CARBOHYDRAZIDE;4-Methyl-2-phenylthiazole-5-carboxylic acid hydrazide
• CAS NO: 61292-08-8
• Molecular Formula: C₁₁H₁₁N₃OS
• Molecular Weight: 233.29
• Mol File: 61292-08-8.mol

Chemical Properties

• Appearance: /
• Density: 1.287g/cm³
• Refractive Index: 1.632
• CAS DataBase Reference: 4-METHYL-2-PHENYL-1,3-THIAZOLE-5-CARBOHYDRAZIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-METHYL-2-PHENYL-1,3-THIAZOLE-5-CARBOHYDRAZIDE(61292-08-8)
• EPA Substance Registry System: 4-METHYL-2-PHENYL-1,3-THIAZOLE-5-CARBOHYDRAZIDE(61292-08-8)

Safety Data

• Hazardous Substances Data: 61292-08-8(Hazardous Substances Data)

Usage

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.

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)

Upstream product

• 2227-79-4 benzenecarbothioamide 
• 53715-64-3 4-methyl-2-phenyl-thiazole-5-carboxylic acid ethyl ester 

Downstream Products

• 219860-18-1 4-methyl-3-(4-methyl-2-phenylthiazol-5-yl)-1H-1,2,4-triazol-5(4H)-thione 
• 400082-03-3 4-allyl-3-(4-methyl-2-phenylthiazol-5-yl)-1H-1,2,4-triazol-5(4H)-thione 
• 1428354-62-4 potassium 2-(4-methyl-2-phenylthiazol-5-carbonyl)-hydrazinecarbodithioate 
• 219860-16-9 1-(4-methyl-2-phenylthiazol-5-carbonyl)-4-methylthiosemicarbazide 
• 1428354-68-0 4-allyl-1-(4-methyl-2-phenylthiazol-5-carbonyl)-thiosemicarbazide 

Relevant articles and documents

New thiazolyl-triazole Schiff bases: Synthesis and evaluation of the anti-Candida potential

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

Synthesis and evaluation of antimicrobial activity of some new hetaryl-azoles derivatives obtained from 2-aryl-4-methylthiazol-5- carbohydrazides and isonicotinic acid hydrazide

A series of new 1,3,4-oxadiazole/thiadiazole and 1,2,4-triazole derivatives have been synthesized starting from 2-aryl-4-methylthiazol-5-carbohydrazides and isonicotinic acid hydrazide. All the newly synthesized compounds were characterized by IR, 1