62124-43-0

Basic information

• Product Name: 2-CHLORO-5-PHENYLTHIAZOLE
• Synonyms: 2-CHLORO-5-PHENYL-1,3-OXAZOLE;2-CHLORO-5-PHENYLOXAZOLE;2-CHLORO-5-PHENYLTHIAZOLE;6-BroMo-2-Methyl-3h-IMidazol[4,5-B]Pyridine
• CAS NO: 62124-43-0
• Molecular Formula: C₉H₆ClNO
• Molecular Weight: 195.67
• Mol File: 62124-43-0.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 310.927°C at 760 mmHg
• Flash Point: 141.844°C
• Appearance: /
• Density: 1.259g/cm³
• Vapor Pressure: 0.001mmHg at 25°C
• Refractive Index: 1.56
• Storage Temp.: Sealed in dry,Store in freezer, under -20°C
• CAS DataBase Reference: 2-CHLORO-5-PHENYLTHIAZOLE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-CHLORO-5-PHENYLTHIAZOLE(62124-43-0)
• EPA Substance Registry System: 2-CHLORO-5-PHENYLTHIAZOLE(62124-43-0)

Safety Data

• Hazardous Substances Data: 62124-43-0(Hazardous Substances Data)

Usage

Uses

2-Chloro-5-phenyloxazole is a useful research chemical.

InChI:InChI=1/C9H6ClNO/c10-9-11-6-8(12-9)7-4-2-1-3-5-7/h1-6H

Upstream product

• 129053-63-0 1-benzoyl-3-chloro-1,2,4-triazole 
• 1006-68-4 5-phenyloxazole 
• 16172-23-9 5-phenyl-1,3-oxazole-2-thiol 
• 5468-37-1 2-aminoacetophenone hydrochloride 
• 98-88-4 benzoyl chloride 
• 16172-23-9 5-phenyl-3H-oxazole-2-thione 

Downstream Products

• 122320-93-8 4-{2-[Methyl-(5-phenyl-oxazol-2-yl)-amino]-ethoxy}-benzaldehyde 
• 862599-57-3 2''-chloro-5-phenyl-[2,4';2',4'']trisoxazole 
• 862599-56-2 5-phenyl-[2,4';2',4'']trisoxazole 

Relevant articles and documents

CALPAIN MODULATORS AND THERAPEUTIC USES THEREOF

Disclosed herein are small molecule calpain modulator compositions, pharmaceutical compositions, the use and preparation thereof.

Arylpiperaszine derivatives, to the process for the production thereof and to the use thereof as therapeutic agents

The invention relates to compounds of the general formula (I): to the process for preparing them, and to the use thereof as a therapeutic agent.

A two-stage iterative process for the synthesis of poly-oxazoles

(Chemical Equation Presented) Methodology has been developed to prepare bis-oxazoles via a two-stage iterative process. The sequence begins with C 2-chlorination of a lithiated oxazole using hexachloroethane. Generation of the C2-Cs