1427-06-1

Basic information

• Product Name: 6-FLUORONICOTINIC ACID METHYL ESTER
• Synonyms: 6-FLUORONICOTINIC ACID METHYL ESTER;METHYL6-FLUORONICOTINATE;Methyl 6-fluoropyridine-3-carboxylate;3-Pyridinecarboxylic acid, 6-fluoro-, methyl ester;Methyl 6-fluoropyridine-3-carboxylate, 6-Fluoro-3-(methoxycarbonyl)pyridine;6-fluoro-3-Pyridinecarboxylic acid Methyl ester;6-Fluoro-3-(Methoxycarbonyl)pyridine
• CAS NO: 1427-06-1
• Molecular Formula: C₇H₆FNO₂
• Molecular Weight: 155.13
• Product Categories: Pyridine;pharmacetical;Pyridines;Boronic Acid;Picolinic acid series;NULL;Fluorine series;Imidazoles ,Homopiperidines
• Mol File: 1427-06-1.mol

Chemical Properties

• Melting Point: 48-52 °C
• Boiling Point: 210.311 °C at 760 mmHg
• Flash Point: 99 °C
• Appearance: /Solid
• Density: 1.243 g/cm³
• Vapor Pressure: 0.194mmHg at 25°C
• Refractive Index: 1.491
• Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
• Solubility: soluble in Methanol
• PKA: -2.47±0.10(Predicted)
• CAS DataBase Reference: 6-FLUORONICOTINIC ACID METHYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: 6-FLUORONICOTINIC ACID METHYL ESTER(1427-06-1)
• EPA Substance Registry System: 6-FLUORONICOTINIC ACID METHYL ESTER(1427-06-1)

Safety Data

• Hazard Codes: Xn
• Statements: 22-41
• Safety Statements: 26-36/37/39-45
• WGK Germany: 3
• Hazardous Substances Data: 1427-06-1(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
6-Fluoronicotinic acid methyl ester is used as a building block in the synthesis of various pharmaceutical ingredients and agrochemicals, contributing to the development of new and improved chemical compounds.
Used in Pharmaceutical Industry:
6-Fluoronicotinic acid methyl ester is used as a precursor in the production of fluorinated derivatives of nicotinamide, which have been studied for their potential biological activities, including therapeutic applications.
Used in Agrochemical Industry:
6-Fluoronicotinic acid methyl ester is utilized in the synthesis of agrochemicals, enhancing the development of effective and environmentally friendly crop protection agents.

InChI:InChI=1/C7H6FNO2/c1-11-7(10)5-2-3-6(8)9-4-5/h2-4H,1H3

Upstream product

• 93-60-7 methyl 3-pyridinecarboxylate 
• 403-45-2 6-fluoronicotinic acid 
• 74-88-4 methyl iodide 
• 18107-18-1 diazomethyl-trimethyl-silane 

Downstream Products

• 1383798-69-3 (+/-)-3-(6-(3-methyl-1-(4-(6-methylpyridin-3-yl)phenyl)butylamino)nicotinamido)propanoic acid 
• 1383801-02-2 (S)-N-({6-[(3-methyl-1-{4-[5-(trifluoromethyl)pyridin-2-yl]phenyl}butyl)amino]pyridin-3-yl}carbonyl)-β-alanine 
• 1383802-45-6 3-[(6-{(S)-3-methyl-1-[2-(4-trifluoromethyl-phenyl)-pyrimidin-5-yl]-butylamino}-pyridine-3-carbonyl)-amino]-propionic acid 
• 1383801-45-3 (+/-)-6-[(cyclohexyl{2-[4-(trifluoromethyl)phenyl]pyrimidin-5-yl}methyl)amino]nicotinic acid 
• 1383802-59-2 6-{(S)-3-methyl-1-[2-(4-trifluoromethyl-phenyl)-pyrimidin-5-yl]-butylamino}-nicotinic acid 
• 1383802-61-6 3-[(6-{(S)-3-methyl-1-[2-(4-trifluoromethyl-phenyl)-pyrimidin-5-yl]-butylamino}-pyridine-3-carbonyl)-amino]-propionic acid ethyl ester 
• 1383801-20-4 (S)-ethyl N-({6-[(3-methyl-1-{4-[5-(trifluoromethyl)pyridin-2-yl]phenyl}butyl)amino]pyridin-3-yl}carbonyl)-beta-alaninate 
• 1383801-14-6 (S)-methyl 6-[(3-methyl-1-{4-[5-(trifluoromethyl)pyridin-2-yl]phenyl}butyl)amino]nicotinate 
• 89853-71-4 methyl 6-hydrazinyl-3-pyridinecarboxylate 
• 1374891-79-8 (2S,5R)-4-[5-(4-bromo-3-trifluoromethoxy-phenylcarbamoyl)-pyridin-2-yl]-2,5-dimethyl-piperazine-1-carboxylic acid tert-butyl ester 
• 1374883-22-3 ((S)-1-{(S)-2-[4-(4'-{[6-((2R,5S)-2,5-dimethyl-4-methylcarbamoyl-piperazin-1-yl)-pyridine-3-carbonyl]-amino}-2'-trifluoromethoxy-biphenyl-4-yl)-1H-imidazol-2-yl]-pyrrolidine-1-carbonyl}-2-methyl-propyl)-carbamic acid methyl ester 
• 1374892-68-8 (2S,5R)-4-[5-(4'-{2-[(S)-1-((S)-2-methoxycarbonylamino-3-methyl-butyryl)-pyrrolidin-2-yl]-1H-imidazol-4-yl}-2-trifluoromethoxy-biphenyl-4-ylcarbamoyl)-pyridin-2-yl]-2,5-dimethyl-piperazine-1-carboxylic acid tert-butyl ester 
• 201809-22-5 2-{4-[(tert-butoxy)carbonyl]piperazin-1-yl}pyridin-5-carboxylic acid 
• 857284-21-0 tert-butyl 4-(5-(methoxycarbonyl)pyridin-2-yl)piperazine-1-carboxylate 

Relevant articles and documents

Glucagon Receptor Modulators

The present invention provides a compound of Formula (I) or a pharmaceutically acceptable salt thereof wherein R1, R2, R3, A1, A2, A3, A4, L, B1, B2, B3 and B4 are as defined herein. The compounds of Formula I have been found to act as glucagon antagonists or inverse agonists. Consequently, the compounds of Formula I and the pharmaceutical compositions thereof are useful for the treatment of diseases, disorders, or conditions mediated by glucagon.

MODIFIED MALONATE DERIVATIVES

The present invention relates to a novel class of modified malonate derivatives. The modified malonate compounds can be used to treat cancer. The modified malonate compounds can also inhibit histone deacetylase and are suitable for use in selectively inducing terminal differentiation, and arresting cell growth and/or apoptosis of neoplastic cells, thereby inhibiting proliferation of such cells. Thus, the compounds of the present invention are useful in treating a patient having a tumor characterized by proliferation of neoplastic cells. The compounds of the invention may also be useful in the prevention and treatment of TRX-mediated diseases, such as autoimmune, allergic and inflammatory diseases, and in the prevention and/or treatment of diseases of the central nervous system (CNS), such as neurodegenerative diseases. The present invention further provides pharmaceutical compositions comprising the modified malonate derivatives and safe dosing regimens of these pharmaceutical compositions, which are easy to follow, and which result in a therapeutically effective amount of the modified malonate derivatives in vivo.

BENZOTRIAZEPINONE DERIVATIVES

The present invention is concerned with benzotriazepinone derivatives, their intermediates, uses thereof and processes for their production. In particular, the present invention relates to parathyroid hormone (PTH) and parathyroid hormone related protein (PTHrp) receptor ligands, (PTH-1 or PTH/PTHrp receptor ligands). The invention also relates to methods of preparing such ligands and to compounds which are useful as intermediates in such methods.

DIRECT FLUORINATION OF SUBSTITUTED PYRIDINES

The direct fluorination of pyridines bearing alkyl, halogen, ester, or ketone functions has been employed to prepare the corresponding 2-fluoro-substituted pyridines.