79574-70-2

Usage

Uses

Used in Pharmaceutical Industry:
3-Acetyl-2-fluoropyridine is used as an intermediate compound for the synthesis of various pharmaceuticals. Its unique structure and functional groups make it a valuable building block in the development of new drugs, particularly those targeting specific biological pathways or receptors.
Used in Agrochemical Industry:
3-Acetyl-2-fluoropyridine is used as a key component in the production of agrochemicals, such as pesticides and herbicides. Its chemical properties allow it to be incorporated into formulations that can effectively control pests and weeds, contributing to increased crop yields and protection of agricultural resources.
Used in Dye Industry:
3-Acetyl-2-fluoropyridine is used as a precursor in the synthesis of dyes, particularly those with specific color properties or stability. Its presence in the dye molecule can influence the dye's performance, such as its solubility, lightfastness, and resistance to fading.
Used in Detergent Industry:
3-Acetyl-2-fluoropyridine is used as a raw material in the production of detergents, where it can contribute to the formulation's effectiveness in cleaning and stain removal. Its chemical properties may enhance the detergent's ability to break down and remove various types of dirt and grime.
Used in Food Flavoring Industry:
3-Acetyl-2-fluoropyridine is used as a flavoring agent in the food industry, where it can impart specific taste or aroma characteristics to food products. Its unique chemical structure may contribute to the development of new and innovative flavors, enhancing the sensory experience of consumers.

InChI:InChI=1/C7H6FNO/c1-5(10)6-3-2-4-9-7(6)8/h2-4H,1H3

Upstream product

• 79574-61-1 1-(2-Fluoro-3-pyridyl)ethanol 
• 372-48-5 2-fluoropyridine 
• 78191-00-1 N-Methoxy-N-methylacetamide 

Downstream Products

• 65326-33-2 1-(2-amino-3-pyridinyl)-1-ethanone 
• 1125674-06-7 3-methylfuro[2,3-b]pyridine-2-carboxylic acid ethyl ester 
• 174180-77-9 tert-butyl 3-methyl-1H-pyrazolo[3,4-b]pyridine-1-carboxylate 
• 174180-76-8 3-bromomethylpyrazolo[3,4-b]pyridine-1-carboxylic acid tert-butyl ester 
• 1034474-22-0 2-[[(3-{[5-chloro-4-(3-chloro-5-cyanophenoxy)-1H-1,2,3-benzotriazol-1-yl]methyl}-1H-pyrazolo[3,4-b]pyridin-1-yl)carbonyl](methyl)amino]-N-methylethanaminium chloride 
• 1034474-24-2 2-[[(3-{[5-chloro-4-(3-chloro-5-cyanophenoxy)-1H-1,2,3-benzotriazol-1-yl]methyl}-1H-pyrazolo[3,4-b]pyridin-1-yl)carbonyl](methyl)amino]ethanaminium chloride 
• 1034474-45-7 tert-butyl {2-[[(3-{[5-chloro-4-(3-chloro-5-cyanophenoxy)-1H-1,2,3-benzotriazol-1-yl]methyl}-1H-pyrazolo[3,4-b]pyridin-1-yl)carbonyl](methyl)amino]ethyl}methylcarbamate 
• 1034474-46-8 tert-butyl {2-[[(3-{[5-chloro-4-(3-chloro-5-cyanophenoxy)-1H-1,2,3-benzotriazol-1-yl]methyl}-1H-pyrazolo[3,4-b]pyridin-1-yl)carbonyl](methyl)amino]ethyl}carbamate 
• 1034474-40-2 tert-butyl 3-{[5-chloro-4-(3-chloro-5-cyanophenoxy)-1H-1,2,3-benzotriazol-1-yl]methyl}-1H-pyrazolo[3,4-b]pyridine-1-carboxylate 
• 1034474-33-3 3-chloro-5-{[5-chloro-1-(1-t-butyloxycarbonyl-1H-pyrazolo[3,4-b]pyridin-3-ylmethyl)-1H-indazol-4-yl]oxy}benzonitrile 
• 1034474-21-9 3-chloro-5-{[5-chloro-1-(1H-pyrazolo[3,4-b]pyridin-3-ylmethyl)-1H-1,2,3-benzotriazol-4-yl]oxy}benzonitrile 
• 1034474-19-5 3-chloro-5-{[5-chloro-1-(1H-pyrazolo[3,4-b]pyridin-3-ylmethyl)-1H-indazol-4-yl]oxy}benzonitrile 
• 1303920-16-2 C₂₀H₂₀N₂O₆S₂ 
• 1138033-53-0 2-bromo-1-(2-fluoropyridin-3-yl)ethanone hydrobromide 

Relevant academic research and scientific papers

A facile synthesis of 2,3-disubstituted furo[2,3-b]pyridines

In a three-step sequence starting from readily available starting materials, 2,3-carbon disubstituted furo[2,3-b]pyridines can be accessed in good yields and purity. Furo[2,3-b]pyridines bearing ester, amide and ketone groups at the 2-position can be prepared with a variety of aryl and alkyl groups at the 3-position.

5-Membered heterocyclic compound

The present invention provides 5-membered heterocycle compounds represented by the following general formula (I): The present compounds have a superior acid secretion inhibitory effect, and shows an antiulcer activity and the like.

NON-NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS

Compounds of Formula I: (I), are HIV reverse transcriptase inhibitors, wherein Q, R2, R3, R6, T1, T2, and T3 are defined herein. The compounds of Formula I, and the pharmaceutically accepta

HIV reverse transcriptase inhibitors

Compounds having the structure: are HIV reverse transcriptase inhibitors, wherein A, X, Y, Z, R1 and R2 are defined herein. The compounds and their pharmaceutically acceptable salts are useful in the inhibition of HIV reverse transcriptase, the prophylaxis and treatment of infection by HIV and in the prophylaxis, delay in the onset, and treatment of AIDS. The compounds and their salts can be employed as ingredients in pharmaceutical compositions, optionally in combination with other antivirals, immunomodulators, antibiotics or vaccines.

METALLATION REGIOSELECTIVE EN SERIE PYRIDINIQUE: SYNTHESE ORIGINALE D'AMINO-2-AROYL 3-PYRIDINES

Lithium diisopropylamide reacts with 2-fluoropyridine at low temperature: regioselectivity is excellent and metallation occurs without side reactions such as nucleophilic attack. 2-Fluoro-3-lithiopyridine is formed and with aldehydes it gives the correspo