22620-29-7

Basic information

• Product Name: ETHYL 5-FLUORONICOTINATE
• Synonyms: AURORA KA-3034;ETHYL 5-FLUORONICOTINATE;ETHYL 5-FLUOROPYRIDINE-3-CARBOXYLATE;5-fluoro-3-pyridinecarboxylicaciethylester;ethyl5-fluoro-3-pyridinecarboxylate;Ethyl 5-fluoronicotinate ,98%;5-Fluoropyridine-3-carboxylic acid ethyl ester;3-PYRIDINECARBONYL CHLORIDE, 5-FLUORO-, ETHYL ESTER
• CAS NO: 22620-29-7
• Molecular Formula: C₈H₈FNO₂
• Molecular Weight: 169.15
• Product Categories: Esters;Pyridines
• Mol File: 22620-29-7.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 214 °C at 760 mmHg
• Flash Point: 83.2 °C
• Appearance: /
• Density: 1.197 g/cm³
• Vapor Pressure: 0.159mmHg at 25°C
• Refractive Index: 1.489
• Storage Temp.: 2-8°C
• PKA: 0.88±0.20(Predicted)
• CAS DataBase Reference: ETHYL 5-FLUORONICOTINATE(CAS DataBase Reference)
• NIST Chemistry Reference: ETHYL 5-FLUORONICOTINATE(22620-29-7)
• EPA Substance Registry System: ETHYL 5-FLUORONICOTINATE(22620-29-7)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• HazardClass: IRRITANT
• Hazardous Substances Data: 22620-29-7(Hazardous Substances Data)

Usage

Chemical Properties

Light yellow liquid

InChI:InChI=1/C8H8FNO2/c1-2-12-8(11)6-3-7(9)5-10-4-6/h3-5H,2H2,1H3

Downstream Products

• 118420-35-2 N-[3-(5-fluoro-pyridin-3-yl)acryloyl]-4-(4-diphenylmethyl-1-piperazinyl)butylamine 
• 107756-01-4 C₁₃H₁₂FN₃O₃S 
• 39891-04-8 5-fluoropyridine-3-carboxaldehyde 
• 701-40-6 5-fluoropyridine-3-carbohydrazide 

Relevant articles and documents

Application of trivalent iodine compounds as catalysts in Bal-Schiemann reaction

The invention discloses an application of trivalent iodine compounds shown in formula I and/or II in the description and used as catalysts in Bal-Schiemann reaction. The trivalent iodine compounds areused as the catalysts in the Bal-Schiemann reaction, so that the Bal-Schiemann reaction can be conducted at room temperature or near room temperature when a thermochemical method is used, and the reaction has mild reaction conditions, wide substrate use range and short reaction time, and is safe and easy to operate, products are easy to separate, and raw materials are simple and low in toxicity.