161009-59-2

Upstream product

• 654644-18-5 5-((2-methoxy)ethoxymethoxy)-2-nitrobenzaldehyde 
• 3970-21-6 2-Methoxyethoxymethyl chloride 
• 60463-12-9 3-hydroxymethyl-4-nitrophenol 

Downstream Products

• 161639-17-4 (R)-3-[2-tert-Butoxycarbonylamino-5-(2-methoxy-ethoxymethoxy)-benzyldisulfanyl]-2-(9H-fluoren-9-ylmethoxycarbonylamino)-propionic acid methyl ester 
• 161639-19-6 (S)-2-Amino-4-[(R)-2-[2-tert-butoxycarbonylamino-5-(2-methoxy-ethoxymethoxy)-benzyldisulfanyl]-1-(carboxymethyl-carbamoyl)-ethylcarbamoyl]-butyric acid 
• 161009-71-8 (S)-3-[2-tert-Butoxycarbonylamino-5-(2-methoxy-ethoxymethoxy)-benzyloxy]-2-(9H-fluoren-9-ylmethoxycarbonylamino)-propionic acid methyl ester 
• 161009-69-4 (S)-3-[2-tert-Butoxycarbonylamino-5-(2-methoxy-ethoxymethoxy)-benzyloxy]-2-(9H-fluoren-9-ylmethoxycarbonylamino)-propionic acid 
• 161009-65-0 (S)-3-[2-tert-Butoxycarbonylamino-5-(2-methoxy-ethoxymethoxy)-benzyloxy]-2-(trityl-amino)-propionic acid methyl ester 
• 161009-63-8 (S)-3-[5-(2-Methoxy-ethoxymethoxy)-2-nitro-benzyloxy]-2-(trityl-amino)-propionic acid methyl ester 
• 161639-12-9 [4-(2-Methoxy-ethoxymethoxy)-2-(pyridin-2-yldisulfanylmethyl)-phenyl]-carbamic acid tert-butyl ester 
• 161639-18-5 (R)-2-Amino-3-[2-tert-butoxycarbonylamino-5-(2-methoxy-ethoxymethoxy)-benzyldisulfanyl]-propionic acid 
• 161009-67-2 (S)-2-Amino-3-[2-tert-butoxycarbonylamino-5-(2-methoxy-ethoxymethoxy)-benzyloxy]-propionic acid methyl ester 
• 161639-08-3 Thioacetic acid S-[2-tert-butoxycarbonylamino-5-(2-methoxy-ethoxymethoxy)-benzyl] ester 
• 161639-06-1 [2-Iodomethyl-4-(2-methoxy-ethoxymethoxy)-phenyl]-carbamic acid tert-butyl ester 
• 161639-10-7 [2-Mercaptomethyl-4-(2-methoxy-ethoxymethoxy)-phenyl]-carbamic acid tert-butyl ester 
• 161639-04-9 [2-Hydroxymethyl-4-(2-methoxy-ethoxymethoxy)-phenyl]-carbamic acid tert-butyl ester 
• 161009-61-6 2-Iodomethyl-4-(2-methoxy-ethoxymethoxy)-1-nitro-benzene 

Relevant academic research and scientific papers

Lead structures for applications in photodynamic therapy. Part 2: Synthetic studies for photo-triggered release systems of bioconjugate porphyrin photosensitizers

Photodynamic therapy (PDT) selectivity and specificity can be improved by binding the photosensitizers to target receptors. One approach is to cross-link porphyrins to a biological target receptor via the photocleavable o-nitrobenzyl linker, where a contr

Synthesis of N-protected serine ethers as precursors of new photoactivatable amino acids cleavable by hydrogenolysis

Fmoc-(L)-serine ethers bearing either 2-(2'-methoxyethoxymerhyl ether)-5-terbutyloxycarbonylaminobenzyl (ortho) or 5-(2'-methoxyethoxymethy] ether)-2-terbutyloxycarbonylaminobenzyl (metal moieties were synthesized. Spectral characteristics of the corresponding photoactivatable 4-diazocyclohexa-2,5-dienones were determined.