Kawai, Kentaro et al. published their research in Chemistry – A European Journal in 2018 | CAS: 226260-01-1

3-Fluoro-N-methoxy-N-methylbenzamide (cas: 226260-01-1) belongs to amides. The solubilities of amides and esters are roughly comparable. Typically amides are less soluble than comparable amines and carboxylic acids since these compounds can both donate and accept hydrogen bonds. Tertiary amides, with the important exception of N,N-dimethylformamide, exhibit low solubility in water. Amides are stable compounds. The lower-melting members (such as acetamide) can be readily purified by fractional distillation. Most amides are solids which have low solubilities in water.Recommanded Product: 3-Fluoro-N-methoxy-N-methylbenzamide

Weinreb Amide Directed Versatile C-H Bond Functionalization under (η5-Pentamethylcyclopentadienyl)cobalt(III) Catalysis was written by Kawai, Kentaro;Bunno, Youka;Yoshino, Tatsuhiko;Matsunaga, Shigeki. And the article was included in Chemistry – A European Journal in 2018.Recommanded Product: 3-Fluoro-N-methoxy-N-methylbenzamide This article mentions the following:

The (η5-pentamethylcyclopentadienyl)cobalt(III) (Cp*CoIII)-catalyzed C-H bond functionalization of aromatic, heteroaromatic and α,β-unsaturated Weinreb amides was explored. The C-H allylation using allyl carbonate and a perfluoroalkene/oxidative alkenylation with Et acrylate/iodination using N-iodosuccinimide and amidation with dioxazolones were catalyzed by Cp*Co(CO)I2 in presence of cationic silver salt and silver acetate to afford various synthetically useful building blocks like RC(O)N(Me)(OMe) [R = 2-H2C=CHCH2C6H4, MeC=CHCH=CHCO2Et, 2-I-C6H4, etc.]. Mechanistic studies of C-H allylation disclosed that the C-H activation step was rate determining and virtually irreversible. In the experiment, the researchers used many compounds, for example, 3-Fluoro-N-methoxy-N-methylbenzamide (cas: 226260-01-1Recommanded Product: 3-Fluoro-N-methoxy-N-methylbenzamide).

3-Fluoro-N-methoxy-N-methylbenzamide (cas: 226260-01-1) belongs to amides. The solubilities of amides and esters are roughly comparable. Typically amides are less soluble than comparable amines and carboxylic acids since these compounds can both donate and accept hydrogen bonds. Tertiary amides, with the important exception of N,N-dimethylformamide, exhibit low solubility in water. Amides are stable compounds. The lower-melting members (such as acetamide) can be readily purified by fractional distillation. Most amides are solids which have low solubilities in water.Recommanded Product: 3-Fluoro-N-methoxy-N-methylbenzamide

Referemce:
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics