306936-10-7

Basic information

• Product Name: 2-(2,3-DIHYDRO-1-BENZOFURAN-5-YL)THIAZOLE-4-CARBONYL CHLORIDE
• Synonyms: 2-(2,3-DIHYDRO-1-BENZOFURAN-5-YL)-1,3-THIAZOLE-4-CARBONYL CHLORIDE;2-(2,3-DIHYDRO-1-BENZOFURAN-5-YL)THIAZOLE-4-CARBONYL CHLORIDE;2-(2,3-Dihydrobenzo[b]furan-5-yl)thiazole-4-carbonyl chloride;2-(2,3-Dihydrobenzo[b]furan-5-yl)thiazole-4-carbonyl chloride 95%
• CAS NO: 306936-10-7
• Molecular Formula: C12H8ClNO2S
• Molecular Weight: 265.72
• Mol File: 306936-10-7.mol
• Article Data: 0

Chemical Properties

• Melting Point: 133 °C
• Boiling Point: 429.6°Cat760mmHg
• Flash Point: 213.6°C
• Appearance: /
• Density: 1.444g/cm³
• Vapor Pressure: 1.38E-07mmHg at 25°C
• Refractive Index: 1.645
• PKA: -0.27±0.10(Predicted)
• CAS DataBase Reference: 2-(2,3-DIHYDRO-1-BENZOFURAN-5-YL)THIAZOLE-4-CARBONYL CHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2,3-DIHYDRO-1-BENZOFURAN-5-YL)THIAZOLE-4-CARBONYL CHLORIDE(306936-10-7)
• EPA Substance Registry System: 2-(2,3-DIHYDRO-1-BENZOFURAN-5-YL)THIAZOLE-4-CARBONYL CHLORIDE(306936-10-7)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 306936-10-7(Hazardous Substances Data)

Usage

Description

2-(2,3-Dihydro-1-benzofuran-5-yl)thiazole-4-carbonyl chloride is a chlorinated carbonyl compound characterized by a molecular formula of C13H8ClNO2S. It features a thiazole ring and a benzofuran group, which contribute to its unique chemical properties and reactivity. 2-(2,3-DIHYDRO-1-BENZOFURAN-5-YL)THIAZOLE-4-CARBONYL CHLORIDE is known for its versatility in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals, due to its ability to react with a variety of nucleophiles, facilitating the formation of diverse chemical structures. Furthermore, it has garnered interest for its potential biological activities and pharmacological properties, making it a promising candidate for further research and development.

Uses

Used in Pharmaceutical Industry:
2-(2,3-Dihydro-1-benzofuran-5-yl)thiazole-4-carbonyl chloride is used as a key reagent in the synthesis of various pharmaceutical compounds. Its ability to react with different nucleophiles allows for the creation of a wide range of chemical structures, which can be further utilized in the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 2-(2,3-Dihydro-1-benzofuran-5-yl)thiazole-4-carbonyl chloride serves as an essential intermediate in the production of various agrochemicals. Its reactivity and compatibility with nucleophiles enable the synthesis of novel agrochemicals with improved efficacy and selectivity, contributing to more effective pest control and crop protection strategies.
Used in Organic Synthesis:
2-(2,3-Dihydro-1-benzofuran-5-yl)thiazole-4-carbonyl chloride is employed as a versatile building block in organic synthesis. Its unique structure and reactivity make it suitable for the formation of complex organic molecules, which can be further explored for potential applications in various fields, including materials science, catalysis, and medicinal chemistry.
Used in Biological and Pharmacological Research:
Due to its potential biological activities and pharmacological properties, 2-(2,3-Dihydro-1-benzofuran-5-yl)thiazole-4-carbonyl chloride is utilized in research studies aimed at understanding its interactions with biological systems and identifying its therapeutic potential. This research can lead to the discovery of new drug candidates and the development of innovative therapeutic approaches for various diseases and conditions.

InChI:InChI=1/C12H8ClNO2S/c13-11(15)9-6-17-12(14-9)8-1-2-10-7(5-8)3-4-16-10/h1-2,5-6H,3-4H2