1266683-63-9

Upstream product

• 618-84-8 3-amino-5-nitro-benzoic acid 
• 99-34-3 3,5-dinitrobenzoic acid 
• 76045-71-1 3-amino-5-hydroxybenzoic acid 
• 78238-14-9 3-hydroxy-5-nitrobenzoic acid 
• 875439-69-3 3-tert-butoxycarbonylamino-5-(tert-butyl-diphenylsilanyloxy)-benzoic acid methyl ester 
• 1452402-95-7 C₂₄H₂₇NO₃Si 
• 1452402-96-8 C₂₄H₂₅N₃O₃Si 

Downstream Products

• 1266683-65-1 methyl 3-azido-5-isobutoxybenzoate 
• 1266683-66-2 methyl 3-(4-(3-(N-Boc-amino)-5-isobutoxyphenyl)-1H-1,2,3-triazol-1-yl)-5-isobutoxybenzoate 
• 1266683-67-3 C₂₈H₃₅ClN₄O₅ 
• 1266683-53-7 C₅₂H₆₄N₈O₉ 
• 1266683-56-0 C₃₈H₄₈BrN₅O₆ 

Relevant academic research and scientific papers

Bioreduction of aryl azides during mutasynthesis of new ansamitocins

Supplementing a culture of a mutant strain of Actinosynnema pretiosum that is unable to biosynthesize aminohydroxy benzoic acid (AHBA), with 3-azido-5-hydroxy-benzoic acid and 3-azido-5-amino-benzoic acid, unexpectedly yielded anilino ansamitocins instead

Halide-guided oligo(aryl-triazole-amide)s foldamers: Receptors for multiple halide ions

We synthesized and characterized a series of oligo(phenyl-amide-triazole)s that can fold into a helical conformation guided by halide ions. Their binding models and affinities are highly dependent on the length of the foldamer, media and the inducing capa