30148-19-7

Basic information

• Product Name: CHEMBRDG-BB 5544135
• Synonyms: CHEMBRDG-BB 5544135;OTAVA-BB BB7020210424;(2-FLUOROPHENYL)(1-METHYL-1H-IMIDAZOL-2-YL)METHANONE;AKOS BBS-00009700;OTAVA-BB 7020210424;(2-fluorophenyl)(1-methyl-1H-imidazol-2-yl)methanone(SALTDATA: FREE)
• CAS NO: 30148-19-7
• Molecular Formula: C₁₁H₉FN₂O
• Molecular Weight: 204.2
• Mol File: 30148-19-7.mol

Chemical Properties

• Boiling Point: 364.8°C at 760 mmHg
• Flash Point: 174.4°C
• Appearance: /
• Density: 1.21g/cm³
• Vapor Pressure: 1.64E-05mmHg at 25°C
• Refractive Index: 1.579
• CAS DataBase Reference: CHEMBRDG-BB 5544135(CAS DataBase Reference)
• NIST Chemistry Reference: CHEMBRDG-BB 5544135(30148-19-7)
• EPA Substance Registry System: CHEMBRDG-BB 5544135(30148-19-7)

Safety Data

• Hazard Codes: Xn
• Statements: 22
• Hazardous Substances Data: 30148-19-7(Hazardous Substances Data)

Usage

InChI:InChI=1/C11H9FN2O/c1-14-7-6-13-11(14)10(15)8-4-2-3-5-9(8)12/h2-7H,1H3

Upstream product

• 616-47-7 1-methyl-1H-imidazole 
• 393-52-2 2-Fluorobenzoyl chloride 

Relevant articles and documents

Ruthenium(II)-catalyzed arylation of ortho-CH Bonds in 2-aroyl-imidazoles with aryl halides

The ruthenium(II)-catalyzed ortho-CH arylation of 2-aroyl-imidazoles with aryl bromides and chloride is reported. An imidazole ring functions both as a masked ester and a directing group for CH activation. A variety of functional groups are tolerated unde

Base-Promoted Amidation and Esterification of Imidazolium Salts via Acyl C-C bond Cleavage: Access to Aromatic Amides and Esters

Imidazolium salts have been effectively employed as suitable acyl transfer agents in amidation and esterification in organic synthesis. The weak acyl C(O)-C imidazolium bond was exploited to generate acyl electrophiles, which further react with amines and alcohols to afford amides and esters. The broad substrate scope of anilines and benzylic amines and base-promoted conditions are the benefits of this route. Interestingly, phenol, benzylic alcohols, and a biologically active alcohol can also be subjected to esterification under the optimized conditions.