58402-70-3

Upstream product

• 109-87-5 Dimethoxymethane 
• 14472-14-1 4-bromo-3-methylphenol 

Downstream Products

• 1258595-03-7 1-ethynyl-4-(methoxymethoxy)-2-methylbenzene 
• 1258595-04-8 3-chloro-5-((4-(methoxymethoxy)-2-methylphenyl)ethynyl)picolinonitrile 
• 1258595-05-9 ethyl 3-(5-amino-2-((4-(methoxymethoxy)-2-methylphenyl)ethynyl)-benzo[f][1,7] naphthyridin-8-yl)propanoate 
• 1258595-06-0 ethyl 3-(5-amino-2-(4-(methoxymethoxy)-2-methylphenethyl)benzo[f][1,7]naphthyridin-8-yl)propanoate 
• 1258595-02-6 triethyl((4-(methoxymethoxy)-2-methylphenyl)ethynyl)silane 
• 1268527-08-7 ethyl 3-(5-amino-2-(4-(2-(3-(diethoxyphosphoryl)-3,3-difluoropropoxy)ethoxy)-2-methylphenethyl)benzo[f][1,7]naphthyridin-8-yl)propanoate 
• 1258595-14-0 3-(5-amino-2-(4-(2-(3,3-difluoro-3-phosphonopropoxy)ethoxy)-2-methylphenethyl)benzo[f][1,7]naphthyridin-8-yl)propanoic acid 
• 1258595-15-1 3-(5-amino-2-(2-methyl-4-(2-(2-(2-phosphonoethoxy)ethoxy)ethoxy)phenethyl) benzo[f][1,7]naphthyridin-8-yl)propanoic acid 
• 1268527-10-1 ethyl 3-(5-amino-2-{2-[4-(2-{2-[2-(diethoxyphosphoryl)ethoxy]ethoxy}ethoxy)-2-methylphenyl]ethyl}benzo[f][1,7]naphthyridin-8-yl)propanoate 
• 1258595-07-1 ethyl 3-(5-amino-2-(4-hydroxy-2-methylphenethyl)benzo[f]-[1,7]naphthyridin-8-yl)propanoate 
• 1454658-10-6 3-(5-amino-2-(2-methyl-4-(2-(2-(2-phosphonoethoxy)ethoxy)ethoxy)phenethyl) benzo[f][1,7]naphthyridin-8-yl)propanoic acid, L-arginine salt 
• 1392223-06-1 tert-butyl (2-(2-(2-((2-bromo-5-(methoxymethoxy)benzyl)oxy)ethoxy)ethoxy)ethyl)carbamate 
• 1392223-05-0 1-bromo-2-(bromomethyl)-4-(methoxymethoxy)benzene 
• 1392223-12-9 S-(4-(2-((4-nitrobenzyl)amino)-2-oxoethyl)phenyl) (E)-3-(2-(14,14-dimethyl-12-oxo-2,5,8,13-tetraoxa-11-azapentadecyl)-4-(methoxymethoxy)phenyl)prop-2-enethioate 

Relevant academic research and scientific papers

Development of protein-labeling probes with a redesigned fluorogenic switch based on intramolecular association for no-wash live-cell imaging

Turn on the switch: Fluorogenic probes for protein labeling based on the photoactive yellow protein (PYP) tag were developed. The fluorescence of the probes is turned off by intramolecular association and switched on by the reversal of this interaction up

Syntheses of sterically hindered pyridinium phenoxides as model compounds in nonlinear optics

Noncentrosymmetric molecules with a π-conjugated system and, among them, push-pull molecules such as pyridinium phenoxide, are a promising new class of materials for applications in optoelectronics due to their nonlinear optical (NLO) properties. Modelling studies have indicated that an increase in the twist angle between the two aromatic rings leads to an enhancement of the NLO properties. In order to confirm this feature experimentally, it was necessary to prepare a series of new hindered pyridinium phenoxides. Their efficient syntheses by Suzuki cross-coupling reactions are described herein. Wiley-VCH Verlag GmbH & Co. KGaA, 2006.