101603-37-6

Basic information

• Product Name: ethyl 2-(N-acetamido)-2-(carboxyethyl)-4-(4-nitrophenyl)butanoate
• Synonyms: ethyl 2-(N-acetamido)-2-(carboxyethyl)-4-(4-nitrophenyl)butanoate
• CAS NO: 101603-37-6
• Molecular Weight: 366.371
• Mol File: 101603-37-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: ethyl 2-(N-acetamido)-2-(carboxyethyl)-4-(4-nitrophenyl)butanoate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 2-(N-acetamido)-2-(carboxyethyl)-4-(4-nitrophenyl)butanoate(101603-37-6)
• EPA Substance Registry System: ethyl 2-(N-acetamido)-2-(carboxyethyl)-4-(4-nitrophenyl)butanoate(101603-37-6)

Safety Data

• Hazardous Substances Data: 101603-37-6(Hazardous Substances Data)

Upstream product

• 100-27-6 2-(4-nitrophenyl)ethanol 
• 104-03-0 4-nitrobenzeneacetic acid 
• 103-63-9 1-phenyl-2-bromoethane 
• 60-12-8 2-phenylethanol 
• 50434-36-1 4-nitrophenylacetyl chloride 
• 5339-26-4 (4-nitrophenyl)ethyl bromide 
• 1068-90-2 2-acetylaminomalonic acid diethyl ester 

Downstream Products

• 139879-17-7 DL-4-(4-aminophenyl)-2-aminobutanoic acid 
• 855650-50-9 acetylamino-{4-[bis-(2-hydroxy-ethyl)-amino]-phenethyl}-malonic acid diethyl ester 
• 103530-50-3 (S)-2-acetylamino-4-(4-nitro-phenyl)-butyric acid 
• 191864-33-2 1-methyl-4-[(4-nitrophenyl)ethyl]imidazolidine-2,5-dione 
• 191864-31-0 4-(4-nitrophenethyl)-1,3-oxazolidin-2-one 
• 191864-30-9 2-amino-4-(4-nitrophenyl)butanol 
• 860374-40-9 acetylamino-(4-amino-phenethyl)-malonic acid diethyl ester 
• 139973-76-5 DL-4-(4-nitrophenyl)-2-aminobutanoic acid 
• 103451-59-8 (+/-)-2-acetylamino-4-(4-nitro-phenyl)-butyric acid 

Relevant articles and documents

Bimodal ligands with macrocyclic and acyclic binding moieties, complexes and compositions thereof, and methods of using

Substituted 1,4,7-triazacyclononane-N,N′,N″-triacetic acid and 1,4,7,10-tetraazacyclcododecane-N,N′,N″,N′″-tetraacetic acid compounds with a pendant amino or hydroxyl group, metal complexes thereof, compositions thereof, and methods of making and use in diagnostic imaging and treatment of cellular disorders.

Biosynthesis of the Antibiotic Obafluorin from p-Aminophenylalanine and Glycine (Glyoxylate)

Results of experiments using 'resting' cells of Pseudomonas fluorescens with -, - and 2H2>-glycine as precursors show that glyoxylic acid is specifically the source of C-1 and C-2 of the antibiotic obafluorin 1.The 13C labelling patterns are consistent with the passage of the precursors through the tartronic semialdehyde and glyoxylate pathways.The glycine derivative 6 is not a precursor for 1.The analogues 24 and 25 of p-aminophenylalanine 3 are synthesised and tested as substrates for biosynthesis in P. fluorescens.With 24, the metabolite 26 is detected; no metabolites of 25 are detected.