198967-24-7

Basic information

• Product Name: 2-Fluoro-N-methoxy-N-methylbenzamide
• Synonyms: 2-FLUORO-N-METHOXY-N-METHYLBENZAMIDE;2-Fluoro-N-methoxy-N-metylbenzamide ;N-Methoxy-N-Methyl-2-fluorobenzaMide;FMMB 3-Fluoro-n-methoxy-n-methylbenzamide
• CAS NO: 198967-24-7
• Molecular Formula: C₉H₁₀FNO₂
• Molecular Weight: 183.18
• Mol File: 198967-24-7.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 299.9 °C at 760 mmHg
• Flash Point: 135.2 °C
• Appearance: /
• Density: 1.179 g/cm³
• Vapor Pressure: 0.00116mmHg at 25°C
• Refractive Index: 1.509
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 2-Fluoro-N-methoxy-N-methylbenzamide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Fluoro-N-methoxy-N-methylbenzamide(198967-24-7)
• EPA Substance Registry System: 2-Fluoro-N-methoxy-N-methylbenzamide(198967-24-7)

Safety Data

• Hazardous Substances Data: 198967-24-7(Hazardous Substances Data)

Usage

General Description

2-Fluoro-N-methoxy-N-methylbenzamide is a chemical compound with the molecular formula C9H10FNO2. It is a benzamide derivative with a fluorine atom attached to the second carbon and a methoxy and methyl group attached to the nitrogen atom. 2-Fluoro-N-methoxy-N-methylbenzamide is commonly used in organic synthesis and medicinal chemistry research. It is known to have potential pharmacological activities, including analgesic and anti-inflammatory properties. Additionally, it is used as a building block in the development of new pharmaceuticals and agrochemicals. Overall, 2-Fluoro-N-methoxy-N-methylbenzamide is an important chemical with various applications in the fields of medicine and industry.

InChI:InChI=1/C9H10FNO2/c1-11(13-2)9(12)7-5-3-4-6-8(7)10/h3-6H,1-2H3

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Relevant articles and documents

Flow Microreactor Technology for Taming Highly Reactive Chloroiodomethyllithium Carbenoid: Direct and Chemoselective Synthesis of α-Chloroaldehydes

A straightforward flow synthesis of α-chloro aldehydes has been developed. The strategy involves, for the first time, the thermal unstable chloroiodomethyllithium carbenoid and carbonyl compounds. A batch versus flow comparative study showcases the superb capability of flow technology in prolonging the lifetime of the lithiated carbenoid, even at -20 °C. Remarkably, the high chemoselectivity realized in flow allowed for preparing polyfunctionalized α-chloro aldehydes not easily accessible with traditional batch procedures.

PIPERIDINE-DIONE DERIVATIVES

The invention provides novel compounds having the general formula (I) and tautomers and pharmaceutically acceptable salts thereof, wherein A1, A2, A3, A4, R1, R4, R5, R6, R7 and R8 are as defined herein, compositions including the compounds and methods of using the compounds.

Highly efficient and environmentally benign preparation of Weinreb amides in the biphasic system 2-MeTHF/water

A straightforward chromatography-free preparation of Weinreb amides starting from acid halides has been achieved in the biphasic medium 2-MeTHF/water. Analytically pure compounds were isolated in excellent yields simply after removal of 2-MeTHF, which abs