341925-61-9

Basic information

• Product Name: 3-(N-tert-butoxycarbonylamino)-5-aminobenzoic acid ethyl ester
• Synonyms: 3-(N-tert-butoxycarbonylamino)-5-aminobenzoic acid ethyl ester
• CAS NO: 341925-61-9
• Molecular Weight: 280.324
• Mol File: 341925-61-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 3-(N-tert-butoxycarbonylamino)-5-aminobenzoic acid ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(N-tert-butoxycarbonylamino)-5-aminobenzoic acid ethyl ester(341925-61-9)
• EPA Substance Registry System: 3-(N-tert-butoxycarbonylamino)-5-aminobenzoic acid ethyl ester(341925-61-9)

Safety Data

• Hazardous Substances Data: 341925-61-9(Hazardous Substances Data)

Upstream product

• 535-87-5 3.5-diaminobenzoic acid 
• 24424-99-5 di-tert-butyl dicarbonate 
• 1949-51-5 3,5-diaminobenzoic acid ethyl ester 

Downstream Products

• 341925-78-8 3-[N-(N-tert-butoxycarbonyl-L-alanyl)amino]-5-(N'-palmitoylamino)benzoicacid ethyl ester 
• 341925-64-2 3-[N-(N-tert-butoxycarbonyl-L-alanyl)amino]-5-(N'-decanoylamino)benzoic acid ethyl ester 
• 791772-79-7 3-amino-5-(N-hexadecanoylamino)benzoic acid ethyl ester 
• 767620-13-3 3-amino-5-(N-decanoylamino)benzoic acid ethyl ester 
• 195970-81-1 3-[N-(N-tert-butoxycarbonyl-L-alanyl)amino]-5-(N'-hexadecanoylamino)benzoic acid 
• 195970-80-0 3-[N-(N-tert-butoxycarbonyl-L-alanyl)amino]-5-(N'-decanoylamino)benzoic acid 
• 341925-76-6 3-(N-tert-butoxycarbonylamino)-5-(N'-hexadecanoylamino)benzoic acid ethyl ester 
• 341925-62-0 3-(N-tert-butoxycarbonylamino)-5-(N'-decanoylamino)benzoic acid ethyl ester 

Relevant articles and documents

Factors influencing the activity of nanozymes in the cleavage of an RNA model substrate

A series of 2-nm gold nanoparticles passivated with different thiols all featuring at least one triazacyclonanone-Zn(II) complex and different flanking units (a second Zn(II) complex, a triethyleneoxymethyl derivative or a guanidinium of arginine of a peptide) were prepared and studied for their efficiency in the cleavage of the RNA-model substrate 2-hydroxypropyl-p-nitrophenyl phosphate. The source of catalysis for each of them was elucidated from the kinetic analysis (Michaelis–Menten profiles, pH dependence and kinetic isotope effect). The data indicated that two different mechanisms were operative: One involving two Zn(II) complexes and the other one involving a single Zn(II) complex and a flanking guanidinium cation. The mechanism based on a dinuclear catalytic site appeared more efficient than the one based on the cooperativity between a metal complex and a guanidinium.