38518-55-7

Upstream product

• 609-65-4 o-chlorobenzoyl chloride 
• 5619-04-5 methyl 2-amino-3-hydroxypropanoate hydrochloride 
• 5680-80-8 methyl (2S)-2-amino-3-hydroxypropanoate hydrochloride 
• 118-91-2 ortho-chlorobenzoic acid 

Downstream Products

• 38524-11-7 3-Chloro-2-(2-chloro-benzoylamino)-propionic acid methyl ester 
• 913713-16-3 (S)-2-(2-chlorophenyl)-4-methoxycarbonyl-4,5-dihydro-1,3-oxazole 
• 38524-32-2 methyl 2-(2-chlorobenzamido)-2-propenoate 
• 1383581-71-2 N-hydroxy-2-(2-chlorophenyl)oxazole-4-carboxamide 
• 1247706-41-7 2-(2-chlorophenyl)oxazole-4-carboxylic acid 
• 1370731-57-9 methyl 2-(2-chlorophenyl)oxazole-4-carboxylate 

Relevant academic research and scientific papers

Hydroxamic Acids as Potent Inhibitors of FeII and MnII E. coli Methionine Aminopeptidase: Biological Activities and X-ray Structures of Oxazole Hydroxamate-EcMetAP-Mn Complexes

New series of acids and hydroxamic acids linked to five-membered heterocycles including furan, oxazole, 1,2,4- or 1,3,4-oxadiazole, and imidazole were synthesized and tested as inhibitors against the FeII, CoII, and MnII f

Chiral Phosphinophenyloxazolines bearing alkoxymethyl substituants: Synthesis and application in the palladium catalyzed allylic substitution reactions

The chiral phos phine-oxazoline ligands 3 and 4 bearing 4-alkoxymethyl sub stitu ents on the oxazoline ring with (R)-configuration were prepared from L-serine methyl ester in 66% and 33% yields, respectively. Along this synthetic path way, the β-hydroxyla