131605-29-3

Upstream product

• 98017-92-6 2-phenyl-1,3-propanediol diacetate 
• 108-24-7 acetic anhydride 
• 91748-03-7 1,3-dihydroxy-2-(4-nitrophenyl)propane 
• 1570-95-2 2-phenylpropane-1, 3-diol 

Downstream Products

• 131605-30-6 1,3-diacetoxy-2-(4-aminophenyl)propane 
• 131605-42-0 Acetic acid 3-hydroxy-2-(4-nitro-phenyl)-propyl ester 
• 131605-42-0 Acetic acid (R)-3-hydroxy-2-(4-nitro-phenyl)-propyl ester 
• 131682-39-8 Acetic acid (S)-3-hydroxy-2-(4-nitro-phenyl)-propyl ester 
• 91748-03-7 1,3-dihydroxy-2-(4-nitrophenyl)propane 
• 131605-31-7 1,3-diacetoxy-2-(4-acetamidophenyl)propane 
• 131605-46-4 Acetic acid 2-(4-acetylamino-phenyl)-3-hydroxy-propyl ester 

Relevant academic research and scientific papers

Ferrocenyl derivatives with one, two, or three sulfur-containing arms for self-assembled monolayer formation

Self-assembled monolayers of electroactive molecules can form on gold electrodes if the molecules include a sulfur-containing group to coordinate with the gold surface. We have prepared a molecule with a tripod of sulfur groups that has the potential of fixing the geometry of the molecule relative to the gold surface. The target (3) contained the good one-electron donor ferrocene connected through a benzene spacer to an isobutane tripod, with each arm of the tripod ending in a methylthio group. Analogous compounds with one (1) and two (2) coordinating arms were also prepared.

Reducing ion channel activity in a series of 4-heterocyclic arylamide FMS inhibitors

During efforts to improve the bioavailability of FMS kinase inhibitors 1 and 2, a series of saturated and aromatic 4-heterocycles of reduced basicity were prepared and evaluated in an attempt to also improve the cardiovascular safety profile over lead ary

Enzyme catalyzed monohydrolysis of 2-aryl-1 3-propanediol diacetates. A study of structural effects of the aryl moiety on the enantioselectivity

PPL catalyzed monohydrolysis of 2-aryl substituted 13-propanediol diacetates afforded the corresponding monoacetates in acceptable to fair chemical and optical yields. Electronic effects in the aromatic ring were examined. Elaboration of some 2-arylpropanediol monoacetates to optically active 2-arylpropanols and propanoic acids was performed.