153492-20-7

Basic information

• Product Name: 2-{[5-(Acetyl-benzyloxy-amino)-pentylcarbamoyl]-methyl}-N-{5-[benzyloxy-(3-methoxycarbonyl-propionyl)-amino]-pentyl}-2-hydroxy-succinamic acid tert-butyl ester
• CAS NO: 153492-20-7
• Molecular Weight: 784.948
• Mol File: 153492-20-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-{[5-(Acetyl-benzyloxy-amino)-pentylcarbamoyl]-methyl}-N-{5-[benzyloxy-(3-methoxycarbonyl-propionyl)-amino]-pentyl}-2-hydroxy-succinamic acid tert-butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-{[5-(Acetyl-benzyloxy-amino)-pentylcarbamoyl]-methyl}-N-{5-[benzyloxy-(3-methoxycarbonyl-propionyl)-amino]-pentyl}-2-hydroxy-succinamic acid tert-butyl ester(153492-20-7)
• EPA Substance Registry System: 2-{[5-(Acetyl-benzyloxy-amino)-pentylcarbamoyl]-methyl}-N-{5-[benzyloxy-(3-methoxycarbonyl-propionyl)-amino]-pentyl}-2-hydroxy-succinamic acid tert-butyl ester(153492-20-7)

Safety Data

• Hazardous Substances Data: 153492-20-7(Hazardous Substances Data)

Upstream product

• 153492-04-7 2-Hydroxy-1,2,3-propanetricarboxylic acid 2-tert-butyl 1,3-bis(p-nitrophenyl) triester 
• 153492-08-1 1-<(tert-Butoxycarbonyl)amino>-5-<(trichloroethoxycarbonyl)(benzyloxy)amino>pentane 
• 153492-10-5 N-Benzyloxy-N-(5-tert-butoxycarbonylamino-pentyl)-succinamic acid methyl ester 
• 153492-09-2 1-<(tert-Butoxycarbonyl)amino>-5-<(benzyloxy)amino>pentane 
• 114340-51-1 2-tert-butyl 1,3-dimethyl 2-hydroxypropane-1,2,3-tricarboxylate 
• 83948-51-0 1-<(tert-Butoxycarbonyl)amino>-5-pentane 
• 83966-23-8 1-Amino-5-pentane 
• 83948-54-3 tert-butyl (5-bromopentyl)carbamate 
• 114340-52-2 3-(tert-butoxycarbonyl)-3-hydroxypentanedioic acid 
• 75178-90-4 N-(tert-butyloxycarbonyl)-5-aminopentanol 
• 90195-00-9 N-<(2,2,2-trichloroethoxy)carbonyl>-O-benzylhydroxylamine 
• 53798-96-2 1,5-dimethyl citrate 
• 153492-11-6 N-(5-Amino-pentyl)-N-benzyloxy-succinamic acid methyl ester 
• 153492-07-0 2-{[5-(Acetyl-benzyloxy-amino)-pentylcarbamoyl]-methyl}-2-hydroxy-succinic acid 1-tert-butyl ester 4-(4-nitro-phenyl) ester 

Relevant articles and documents

Synthesis of Novel Citrate-Based Siderophores and Siderophore-β-Lactam Conjugates. Iron Transport-Mediated Drug Delivery Systems

The synthesis of analogs of arthrobactin (5), a microbial iron chelator, and its imide 8 are described.The differentially protected citric acid residue 31 served as the key intermediate in making conjugates having a generalized structure 14 with two representative carbacephalosporin units, 15 and 16.Both conjugates, 49 and 51, showed antibiotic activity, while conjugate 51 obtained from β-lactam 16 bearing a phenylglycyl side chain was shown to be more effective.