10505-59-6

Basic information

• Product Name: 2-[(2Z)-2-imino-1,3-thiazol-3(2H)-yl]-1-phenylethanol
• CAS NO: 10505-59-6
• Molecular Formula: C₁₁H₁₂N₂OS
• Molecular Weight: 220.2908
• Mol File: 10505-59-6.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 383.5°C at 760 mmHg
• Flash Point: 185.7°C
• Density: 1.28g/cm³
• Vapor Pressure: 1.45E-06mmHg at 25°C
• Refractive Index: 1.649
• CAS DataBase Reference: 2-[(2Z)-2-imino-1,3-thiazol-3(2H)-yl]-1-phenylethanol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[(2Z)-2-imino-1,3-thiazol-3(2H)-yl]-1-phenylethanol(10505-59-6)
• EPA Substance Registry System: 2-[(2Z)-2-imino-1,3-thiazol-3(2H)-yl]-1-phenylethanol(10505-59-6)

Safety Data

• Hazardous Substances Data: 10505-59-6(Hazardous Substances Data)

Usage

Antimicrobial Properties

Thiazole-2-imine exhibits the ability to inhibit or kill microorganisms, making it a potential candidate for use in antimicrobial agents.

Antifungal Properties

The compound also demonstrates the ability to counteract the growth of fungi, which can be useful in treating fungal infections.

Pharmaceutical Intermediate

It has been studied for its potential use as a pharmaceutical intermediate, which are compounds used in the synthesis of drugs.

Building Block in Organic Synthesis

Thiazole-2-imine can be used as a starting material or building block in the creation of more complex organic compounds.

Drug Development Potential

The compound has been investigated for its potential role in drug development, particularly in the field of antimicrobial agents.

Value in Chemical and Pharmaceutical Industries

Due to its diverse biological activities and synthetic applications, thiazole-2-imine is considered a valuable compound in both industries.

Upstream product

• 70-11-1 α-bromoacetophenone 
• 116923-07-0 2-amino-3-(2-oxo-2-phenyl-ethyl)-thiazolium; bromide 

Downstream Products

• 6649-73-6 dihydro-5,6 phenyl-6 imidazo<2,1-b>thiazole 

Relevant articles and documents

DIHYDRO-5,6 IMIDAZOTHIAZOLES, DIHYDRO-2,3 IMIDAZOBENZOTHIAZOLES, ANALOGUES DU LEVAMISOLE

New compounds containing 5,6-dihydro imidazothiazole 2,3,5,6-tetrahydro imidazothiazole and 2,3-dihydro imidazobenzothiazole rings, substituted by heterocycles analogue to chromones, were synthesized and screened against three nematodes, in vitro.The results indicate moderate anthelmintic properties, compared to levamisole; nevertheless, some products exhibit a significant degree of activity.