239796-24-8

Upstream product

• 105-13-5 4-Methoxybenzyl alcohol 
• 25506-37-0 4-methoxybenzyl (4-nitrophenyl) carbonate 

Downstream Products

• 239796-25-9 (6-{Amino-[(Z)-4-methoxy-benzyloxycarbonylimino]-methyl}-naphthalen-2-yloxy)-acetic acid methyl ester 
• 239796-30-6 {6-[imino-(4-methoxy-benzyloxycarbonylamino)-methyl]-naphthalen-2-yloxy}-acetic acid 
• 239796-26-0 [1-Amino-1-(6-benzyloxy-naphthalen-2-yl)-meth-(Z)-ylidene]-carbamic acid 4-methoxy-benzyl ester 
• 239796-27-1 4-(6-{Amino-[(Z)-4-methoxy-benzyloxycarbonylimino]-methyl}-naphthalen-2-yloxymethyl)-benzoic acid methyl ester 
• 239796-28-2 5-(6-{Amino-[(Z)-4-methoxy-benzyloxycarbonylimino]-methyl}-naphthalen-2-yloxy)-pentanoic acid ethyl ester 
• 239796-29-3 4-but-2-enoate 

Relevant academic research and scientific papers

Amidine protection for solution phase library synthesis

The application of 4-methoxybenzyl-4-nitrophenylcarbonate as a reagent for the N-protection of amidinonaphthol has been demonstrated. The facile introduction of the 4-methoxybenzyloxycarbonyl group and the mildness of the deprotection conditions make this