13816-04-1

Basic information

• Product Name: 2-ISOPROPENYLTHIAZOLE
• Synonyms: 2-ISOPROPENYLTHIAZOLE;Isopropenylthiazole;2-ISOPROPENYLTHIAZOLE (STABILIZED WITH HQ) 98+%;2-Isopropenylthiazole (stabilized with HQ);2-(Prop-1-en-2-yl)thiazole
• CAS NO: 13816-04-1
• Molecular Formula: C6H7NS
• Molecular Weight: 125.19
• Mol File: 13816-04-1.mol

Chemical Properties

• Boiling Point: 63 °C / 10mmHg
• Appearance: /
• Density: 1,09 g/cm3
• Refractive Index: 1.5550 to 1.5570
• Storage Temp.: Freezer
• CAS DataBase Reference: 2-ISOPROPENYLTHIAZOLE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-ISOPROPENYLTHIAZOLE(13816-04-1)
• EPA Substance Registry System: 2-ISOPROPENYLTHIAZOLE(13816-04-1)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 13816-04-1(Hazardous Substances Data)

Usage

Uses

Used in the Food Industry:
2-Isopropenylthiazole is used as a flavoring agent for its savory, meaty aroma, enhancing the taste and aroma of various food products.
Used in the Perfume Industry:
In the perfume industry, 2-isopropenylthiazole serves as a key component in fragrances, contributing to the creation of unique and appealing scents.
Used in Pharmaceutical Applications:
Due to its chemical structure and reactivity, 2-isopropenylthiazole has potential applications in pharmaceuticals, although further research and development are required to explore its full potential in this field.
Used in Agrochemical Applications:
Similarly, 2-isopropenylthiazole may find use in agrochemicals, but more investigation is needed to determine its specific applications and benefits in this industry.
It is important to handle 2-isopropenylthiazole with caution due to its potential health hazards and flammability.

Upstream product

• 24295-03-2 2-Acetylthiazole 
• 1779-49-3 Methyltriphenylphosphonium bromide 

Relevant articles and documents

Electrochemical fluorosulfonylation of styrenes

An environmentally friendly and efficient electrochemical fluorosulfonylation of styrenes has been developed. With the use of sulfonylhydrazides and triethylamine trihydrofluoride, a diverse array of β-fluorosulfones could be readily obtained. This reaction features mild conditions and a broad substrate scope, which could also be conveniently extended to a gram-scale preparation.

Electrochemistry enabled selective vicinal fluorosulfenylation and fluorosulfoxidation of alkenes

Both sulfur and fluorine play important roles in organic synthesis, the life science, and materials science. The direct incorporation of these elements into organic scaffolds with precise control of the oxidation states of sulfur moieties is of great significance. Herein, we report the highly selective electrochemical vicinal fluorosulfenylation and fluorosulfoxidation reactions of alkenes, which were enabled by the unique ability of electrochemistry to dial in the potentials on demand. Preliminary mechanistic investigations revealed that the fluorosulfenylation reaction proceeded through a radical-polar crossover mechanism involving a key episulfonium ion intermediate. Subsequent electrochemical oxidation of fluorosulfides to fluorosulfoxides were readily achieved under a higher applied potential with the adventitious H2O in the reaction mixture.