5916-12-1

Usage

Uses

Used in Fragrance Industry:
2-Acetylthiophene ethylene acetal is utilized as a fragrance ingredient for its strong, fruity scent, making it suitable for the production of perfumes, soaps, and other personal care products. Its aromatic properties enhance the sensory experience of these products, contributing to their appeal and marketability.
Used in Food Industry:
In the food industry, 2-acetylthiophene ethylene acetal serves as a flavoring agent, adding unique taste profiles to various food products. Its fruity aroma and flavor characteristics make it a valuable component in the creation of diverse culinary experiences.
Used in Organic Synthesis:
2-Acetylthiophene ethylene acetal has applications in organic synthesis, where it acts as a versatile building block for the development of more complex organic compounds. Its reactivity and functional groups make it a useful intermediate in the synthesis of a wide range of chemical products.
Used in Pharmaceutical Production:
As an intermediate in the production of pharmaceuticals, 2-acetylthiophene ethylene acetal plays a crucial role in the synthesis of various medicinal compounds. Its chemical properties allow it to be transformed into active pharmaceutical ingredients, contributing to the development of new drugs and therapies.
Used in Agrochemical Production:
Similarly, in the agrochemical industry, 2-acetylthiophene ethylene acetal is used as an intermediate for the synthesis of various agrochemicals. Its applications extend to the development of pesticides, herbicides, and other agricultural chemicals, enhancing crop protection and yield.
It is important to handle 2-acetylthiophene ethylene acetal with care, as it may cause irritation to the eyes, skin, and respiratory system upon exposure. Proper safety measures should be taken to minimize potential health risks during its use in various applications.

InChI:InChI=1/C8H10O2S/c1-8(9-4-5-10-8)7-3-2-6-11-7/h2-3,6H,4-5H2,1H3

Upstream product

• 88-15-3 2-Acetylthiophene 
• 107-21-1 ethylene glycol 

Downstream Products

• 1026294-56-3 2-[5-(2-Methyl-[1,3]dioxolan-2-yl)-thiophene-2-carbonyl]-benzoic acid 
• 4565-29-1 5-acetylthiophene-2-carbaldehyde 
• 500367-27-1 (4-fluorophenyl)-[5-(2-methyl[1,3]dioxolane-2-yl)thiophene-2-yl]methyl alcohol 
• 1254299-91-6 N-{2-[5-(2-methyl[1,3]dioxolan-2-yl)thiophen-2-yl]benzyl}isobutyrylamide 
• 1440662-59-8 (E)-3-(5-(2-methyl-1,3-dioxolan-2-yl)thiophen-2-yl)-1-phenyl-2-propen-1-one 
• 26170-93-4 2-acetyl-4-phenylthiophene 
• 1426829-21-1 2-[5-(3,5-difluorophenyl)-thiophen-2-yl]-2-methyl-[1,3]-dioxolane 
• 1426829-20-0 2-methyl-2-[5-(2,4,6-trifluorophenyl)thiophen-2-yl]-[1,3]-dioxolane 
• 1426829-15-3 2-methyl-2-[5-(2,3,5-trifluorophenyl)-thiophen-2-yl]-[1,3]-dioxolane 
• 1426829-14-2 C₂₂H₁₈F₄O₄S₂ 
• 1426829-31-3 3-{2,3,6-trifluoro-4-[5-(2-methyl-[1,3]dioxolan-2-yl)thiophen-2-yl]phenyl}pyridine 
• 1426829-25-5 3-{2,3,5,6-tetrafluoro-4-[5-(2-methyl-[1,3]dioxolan-2-yl)thiophen-2-yl]phenyl}pyridine 
• 1426829-24-4 1-{2',3',5',6'-tetrafluoro-4'-[5-(2-methyl-[1,3]dioxolan-2-yl)thiophen-2-yl]-biphenyl-3-yl}ethanone 
• 1426829-23-3 2′,3′,5′,6′-tetrafluoro-4′-[5-(2-methyl-[1,3]dioxolan-2-yl)thiophen-2-yl]biphenyl-4-carbaldehyde 

Relevant academic research and scientific papers

Pharmacological agents and methods of treatment that inactivate pathogenic prokaryotic and eukaryotic cells and viruses by attacking highly conserved domains in structural metalloprotein and metalloenzyme targets

The invention relates to the treatment of viral, bacterial, parasitic, proliferative diseases, neurodegenerative diseases, inflammatory diseases, immunological diseases, transplanted organ rejection, and diseases produced by intoxication with heavy metals. The invention relates to the use of specific metal chelating agents including, furoic acid, 2-thiophenecarboxylic acid and their derivatives, analogs and structurally related chemicals as pharmacological agents that can be used effectively to disrupt and inactivate specific transition metal ion containing zinc finger structural motifs in metalloproteins and specific transition metal ion containing catalytic sites in metalloproteinases, which in turn, inactivate the pathogenic virus, pathogenic prokaryotic or eukaryotic cells which produces disease conditions. The preparations can be administered topically or for systemic use. The preparations are novel wide-spectrum antibiotics which have antiviral, antiproliferative, antineoplastic, antiangiogenic, antibacterial, antiparasitic, antiinfective, and anti-inflammatory effects and can be used in the treatment and prevention of diseases such as AIDS, cancers, untoward angiogenesis, pulmonary anthrax, malaria, inflammatory responses, Alzheimer's disease and other diseases.

CHEMOSELECTIVE PROTECTION OF HETEROAROMATIC ALDEHYDES AS IMIDAZOLIDINE DERIVATIVES. PREPARATION OF 5-SUBSTITUTED FURAN- AND TIOPHENE-2-CARBOXALDEHYDES VIA METALLO-IMIDAZOLIDINE INTERMEDIATES

Furan-, tiophene- and N-methylpyrrole-2-carboxaldehydes may be transformed into the corresponding N,N'-dimethylimidazolidines in a reaction not requiring acid catalysis.The resulting furan and tiophene (but not N-methylpyrrole) derivatives may be metallated in high yields and the carboxaldehyde functionality regenerated under very mild conditions.Treatment of the aldehydoketone 2-acetyl-5-formylthiophene with N,N'-dimethylethylenediamine gives only the product of reaction at the aldehyde function thus establishing this methodology as a potentially valuable method for the protection of an aldehyde in the presence of a ketone.