115299-16-6

Basic information

• Product Name: 2-(2-METHOXY-PHENYL)-THIAZOLE-4-CARBOXYLIC ACID ETHYL ESTER
• Synonyms: 2-(2-METHOXY-PHENYL)-THIAZOLE-4-CARBOXYLIC ACID ETHYL ESTER;ethyl 2-(2-methoxyphenyl)thiazole-4-carboxylate;4-Thiazolecarboxylic acid, 2-(2-methoxyphenyl)-, ethyl ester;ethyl 2-(2-Methoxyphenyl)thiazol-4-carboxylate;2-(2-Methoxyphenyl)-,4-thiazolecarboxylic acid ethyl ester
• CAS NO: 115299-16-6
• Molecular Formula: C₁₃H₁₃NO₃S
• Molecular Weight: 263.31
• Mol File: 115299-16-6.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 408.49°C at 760 mmHg
• Flash Point: 200.848°C
• Appearance: /
• Density: 1.22g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.566
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2-(2-METHOXY-PHENYL)-THIAZOLE-4-CARBOXYLIC ACID ETHYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-METHOXY-PHENYL)-THIAZOLE-4-CARBOXYLIC ACID ETHYL ESTER(115299-16-6)
• EPA Substance Registry System: 2-(2-METHOXY-PHENYL)-THIAZOLE-4-CARBOXYLIC ACID ETHYL ESTER(115299-16-6)

Safety Data

• Hazardous Substances Data: 115299-16-6(Hazardous Substances Data)

Usage

General Description

2-(2-Methoxy-phenyl)-thiazole-4-carboxylic acid ethyl ester is a chemical compound with a molecular formula C13H13NO3S. It is an ethyl ester derivative of thiazole-4-carboxylic acid, which is commonly used in the synthesis of pharmaceuticals and agrochemicals. 2-(2-METHOXY-PHENYL)-THIAZOLE-4-CARBOXYLIC ACID ETHYL ESTER is known for its potential biological activities, such as anti-inflammatory, anti-cancer, and antimicrobial properties. It has also been studied for its potential use in the treatment of various diseases and conditions. Additionally, its ester form makes it suitable for use in organic synthesis and as a building block for the preparation of other chemical compounds.

InChI:InChI=1/C13H13NO3S/c1-3-17-13(15)10-8-18-12(14-10)9-6-4-5-7-11(9)16-2/h4-8H,3H2,1-2H3

Upstream product

• 14214-10-9 ethyl diazopyruvate 
• 42590-97-6 2-methoxythiobenzamide 
• 868-59-7 L-cysteine ethyl ester hydrochloride 
• 135-02-4 ortho-anisaldehyde 
• 70-23-5 ethyl Bromopyruvate 

Downstream Products

• 885279-11-8 2-(2-methoxyphenyl)thiazole-4-carbaldehyde 
• 187793-07-3 2-(2'-methoxyphenyl)-4-hydroxymethylthiazole 

Relevant articles and documents

I2/TBHP-Mediated tandem cyclization and oxidation reaction: Facile access to 2-substituted thiazoles and benzothiazoles

The efficient synthesis of 2-substituted thiazoles and benzothiazoles has been accomplished employing readily available cysteine esters and 2-aminobenzenethiols as N and S sources. The reaction proceeds under an I2/TBHP system and involves a on

PROTEASE INHIBITORS

Disclosed herein is a compound of the formula STR1 known as 2-[N-(N-benzyloxycarbonyl-L-leucinyl)]-2'-[N'-[4-(N,N-dimethylaminomethyl) benzyloxy]carbonyl-L-leucinyl]carbohydrazide; and pharmaceutically acceptable salts, hydrates and solvates thereof.