52894-99-2

Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.

Explanation

This describes the physical appearance of the compound in its solid state.

Explanation

The compound has a range of uses in different industries, making it versatile.

Explanation

The compound contributes to the scent and flavor of various products, such as perfumes and other scented items.

Explanation

The compound serves as a starting material or intermediate in the production of pharmaceuticals and other organic compounds.

Explanation

The compound may pose health risks if not handled with care, emphasizing the importance of proper safety measures during its use.

Appearance

Yellow to orange solid

Industrial applications

Various

Use as a cross-linking agent

Polymer and resin manufacturing

Use in fragrance and flavoring

Perfumes and scented products

Utilization in synthesis

Pharmaceuticals and organic compounds

Health risks

Potential hazards if mishandled or improperly used

Upstream product

• 75-15-0 carbon disulfide 
• 120-46-7 1,3-diphenylpropanedione 
• 74-88-4 methyl iodide 

Downstream Products

• 13636-88-9 3,3-bis(methylthio)-1-phenylprop-2-en-1-one 
• 65-85-0 benzoic acid 
• 128039-46-3 6-benzoyl-5-methylthio-7-phenylpyrazolo<1,5-a>pyrimidine 
• 398117-91-4 diethyl 3,4-diphenylthieno[2,3-b]thiophene-2,5-dicarboxylate 
• 555154-35-3 ethyl 4-benzoyl-5-methylsulfanyl-3-phenylthiophene-2-carboxylate 

Relevant academic research and scientific papers

Palladium-Catalyzed C-S Bond Cleavage with Allenoates: Synthesis of Tetrasubstituted 2-Alkenylfuran Derivatives

Palladium-catalyzed C-S cleavage of tetrasubstituted internal alkene α-oxo ketene dithioacetals was realized with allenoates as the coupling partners, efficiently affording tetrasubstituted 2-alkenylfuran derivatives with excellent regioselectivity under mild conditions. Allenoates acted as C1 synthons in the desulfurative [4 + 1] annulation.

Tin tetrachloride-catalyzed regiospecific allylic substitution of quinone monoketals: An easy entry to benzofurans and coumestans

A highly regioselective allylic substitution of quinone monoketals with a-oxoketene dithioacetals is achieved under the catalysis of only tin tetrachloride (1 mol%). The advantages of the reaction, including its simplicity, rapidity, low catalyst loading of inexpensive tin tetrachloride, mild conditions and; in particular, the regiospecificity, is proposed to be due to a pseudo-intramolecular process. This new synthetic method provides a facile [3+2] cycloaddition route to benzofurans and is highlighted by the synthesis of coumestans.

A convenient synthesis of 2,3,4,5-functionalised thieno[2,3-b]thiophenes

A two steps simple synthesis of 2,3,4,5-functionalised thieno[2,3-b]thiophenes 2-6 from ketene dimethylthioacetals is described.

Application of commercially available anhydrous potassium fluoride for a convenient synthesis of ketene dithioacetals

Commercially available anhydrous KF without activation or solid support promotes condensation between active methylene compounds, carbon disulfide and an alkylating agent in dry DMF to allow the preparation of a variety of ketene dithioacetals in fair to good yields under ambient conditions.

A convenient one-pot synthesis of ketene dithioacetals

An easy synthesis of ketene dithioacetals 2 and 3 by the condensation of carbon disulfide and active methylene compounds 1 with subsequent alkylation in the presence of potassium fluoride is described.