263551-61-7

Basic information

• Product Name: (4-{4-[4-(tert-butoxycarbonylamino-methyl)-phenylamino]-6-chloro-[1,3,5]triazin-2-ylamino}-benzyl)-carbamic acid tert-butyl ester
• Synonyms: (4-{4-[4-(tert-butoxycarbonylamino-methyl)-phenylamino]-6-chloro-[1,3,5]triazin-2-ylamino}-benzyl)-carbamic acid tert-butyl ester
• CAS NO: 263551-61-7
• Molecular Weight: 556.064
• Mol File: 263551-61-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (4-{4-[4-(tert-butoxycarbonylamino-methyl)-phenylamino]-6-chloro-[1,3,5]triazin-2-ylamino}-benzyl)-carbamic acid tert-butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (4-{4-[4-(tert-butoxycarbonylamino-methyl)-phenylamino]-6-chloro-[1,3,5]triazin-2-ylamino}-benzyl)-carbamic acid tert-butyl ester(263551-61-7)
• EPA Substance Registry System: (4-{4-[4-(tert-butoxycarbonylamino-methyl)-phenylamino]-6-chloro-[1,3,5]triazin-2-ylamino}-benzyl)-carbamic acid tert-butyl ester(263551-61-7)

Safety Data

• Hazardous Substances Data: 263551-61-7(Hazardous Substances Data)

Upstream product

• 4403-71-8 (4-aminomethyl)aniline 
• 24424-99-5 di-tert-butyl dicarbonate 
• 108-77-0 1,3,5-trichloro-2,4,6-triazine 
• 94838-55-8 tert-butyl (4-aminobenzyl)carbamate 

Downstream Products

• 263551-66-2 (4-{4-(2-{4,6-bis-[4-(tert-butoxycarbonylamino-methyl)-phenylamino]-[1,3,5]triazin-2-ylamino}-ethylamino)-6-[4-(tert-butoxycarbonylamino-methyl)-phenylamino]-[1,3,5]triazin-2-ylamino}-benzyl)-carbamic acid tert-butyl ester 
• 263551-62-8 (4-{4-(4-amino-benzylamino)-6-[4-(tert-butoxycarbonylamino-methyl)-phenylamino]-[1,3,5]triazin-2-ylamino}-benzyl)-carbamic acid tert-butyl ester 

Relevant articles and documents

Synthesis and characterization of higher generation dendrons based on melamine using p-aminobenzylamine. Evidence for molecular recognition of Cu(II)

The difference in nucleophilicity between the amines of p-aminobenzylamine can be used to synthesize dendrimers based on melamine using a convergent, orthogonal approach. The resulting molecules comprise groups that donate and accept hydrogen-bonds, limiting synthetic accessibility due to intermolecular aggregation. Dendrons with molecular weights exceeding 10 kDa can be prepared by this strategy, but yields drop off significantly at the highest generation (D5) due to difficulties in purification. The addition of Cu(II) reduces the extent of aggregation as evident in SEC traces. UV-vis spectroscopy confirms recognition.