121482-59-5

Basic information

• Product Name: Propanedioic acid, [(2-fluorophenyl)methyl]-, dimethyl ester
• CAS NO: 121482-59-5
• Molecular Formula: C12H13FO4
• Molecular Weight: 240.231
• Mol File: 121482-59-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Propanedioic acid, [(2-fluorophenyl)methyl]-, dimethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Propanedioic acid, [(2-fluorophenyl)methyl]-, dimethyl ester(121482-59-5)
• EPA Substance Registry System: Propanedioic acid, [(2-fluorophenyl)methyl]-, dimethyl ester(121482-59-5)

Safety Data

• Hazardous Substances Data: 121482-59-5(Hazardous Substances Data)

Upstream product

• 345-35-7 2-fluorobenzyl chloride 
• 108-59-8 malonic acid dimethyl ester 
• 446-51-5 2-fluorobenzyl alcohol 
• 18424-76-5 sodiodimethylmalonate 
• 446-48-0 o-fluorobenzyl bromide 

Downstream Products

• 62558-10-5 α-(o-Fluorbenzyl)malonsaeure 
• 1643-26-1 3-(2-fluorophenyl)propionic acid 
• 1269625-86-6 5-(2-fluoro-benzyl)-2-pyridin-2-yl-pyrimidine-4,6-diol 
• 1269626-47-2 5-(2-fluoro-benzyl)-2-(5-fluoro-pyridin-2-yl)-pyrimidine-4,6-diol 
• 1269625-87-7 4,6-dichloro-5-(2-fluoro-benzyl)-2-pyridin-2-yl-pyrimidine 
• 1269625-88-8 4,6-dichloro-5-(2-fluoro-benzyl)-2-(5-fluoro-pyridin-2-yl)-pyrimidine 
• 1269625-97-9 4-{5-[(2-Fluorophenyl)methyl]-6-(morpholin-4-yl)-2-(pyridin-2-yl)pyrimidin-4-yl}morpholine 
• 1269625-99-1 5-(2-Fluoro-benzyl)-6-morpholin-4-yl-2-(5-morpholin-4-yl-pyridin-2-yl)-pyrimidin-4-ylamine 

Relevant articles and documents

Novel Pyrimidine- And Triazine-Hepcidine Antagonists

The present invention relates to new hepcidin antagonists, pharmaceutical compositions containing them and the use thereof as a drug, in particular for the treatment of iron metabolism disorders such as, in particular, iron deficiency diseases and anaemia, in particular anaemia associated with chronic inflammatory disease (ACD: anaemia of chronic disease and AI: anaemia of inflammation).

A facile one-pot benzylation of sodium enolates using trifluoromethansulfonic anhydride and diphenyl sulfoxide

A facile one-pot C-benzylation reaction proceeded smoothly and in good yields by treating various sodium enolates and benzyl alcohol with in situ generated alkoxy diphenyl sulfonium salt derived from trifluoromethansulfonic anhydride and diphenyl sulfoxide.