66735-03-3

Upstream product

• 1009-67-2 2-methyl-3-phenylpropanoic acid 
• 141352-95-6 Diethyl methyl-p-nitrobenzyl-malonate 
• 100-14-1 4-nitrobenzyl chloride 

Downstream Products

• 103096-03-3 (±)-3-(4-aminophenyl)-2-methylpropanoic acid 
• 851968-99-5 (R)-3-(4-nitrophenyl)-2-methylpropanoic acid 
• 120811-86-1 2-methyl-3-(4-nitrophenyl)-1-propanol 
• 62-23-7 4-nitro-benzoic acid 
• 52787-39-0 2-(p-Formylbenzyl)-propionic acid 
• 141352-96-7 2--propionic acid 
• 141352-97-8 2--propionic acid 
• 60423-91-8 rac-3-(4-cyanophenyl)-2-methylpropanoic acid 
• 141352-98-9 2--propionic acid 
• 141352-99-0 1-<4-<2-(Carboxy)-propyl>-benzyl>-1H-1,2,3-triazole 
• 141353-00-6 1-<4-<2-(Carboethoxy)-propyl>-benzyl>-1H-1,2,3-triazole 
• 103096-03-3 (R)-3-(4-amino-phenyl)-2-methyl-propionic acid 

Relevant academic research and scientific papers

An 1,2,3-triazole derivative bioisoster of a potent in vitro prostaglandin synthesis inhibitor: Preparation and biological activity

This paper reports the preparation of the triazole ester 10, a methylenic bioisoster of an oxygenated compound A, effective inhibitor of the prostaglandin synthesis in vitro. Biological evaluation of 10 and of the corresponding acid 9 shows that the compo

Conformational Analysis of 1,1,2-Trisubstituted Ethanes by PMR: Part I - 3-Aryl-2-methylpropanols

A self-consistent model for the conformational analysis of 1,1,2-trisubstituted ethanes is developed, based on the temperature dependence of vicinal proton-proton coupling constants.Synthesis of racemates of 2(R), 3(S)- and 2(S), 3(R)-2,3-dideutero-2-methyl-3-phenyl-1-propanols is accomplished using known reactions of well-defined stereochemistry.By comparing the PMR spectra of undeuterated and deuterated compounds, an unequivocal assignment of benzylic protons is made.Concentration and variable-temperature studies have revealed the existence of very weak intramolecular interaction in three alcohols, p-R-C6H4-CH2-CHMe-CH2-OH, where R = NO2, H and OMe.

Phenylmercaptotetrazolo- and nitroindazolo masked development/image modifiers

Novel nitrobenzyl compounds are incorporated into a photographic emulsion or developer for controlled release of development/image modifier compounds. This occurs imagewise only after developer oxidation products have been formed in the course of the development process. For example, nitrobenzyl-masked phenylmercaptotetrazole (PMT), incorporated into a silver halide emulsion, reacts with developer oxidation products via an electron transfer mechanism to release the potent development restrainer PMT.