114077-01-9

Usage

Chemical Properties

Colourless to yellowish solid

Upstream product

• 56-40-6 glycine 
• 141523-18-4 2-Benzoylamino-3-(4-benzyloxy-2-fluoro-5-methoxyphenyl)acrylic acid 
• 141523-17-3 2-Benzoylamino-3-(4-benzyloxy-2-fluoro-5-methoxyphenyl)acrylic acid azlactone 
• 154051-82-8 N-trifluoroacetyl-3-methoxy-4-trimethylacetoxyphenylalanine ethyl ester 
• 154051-86-2 3-methoxy-4-benzyloxy-6-fluorobenzyl chloride 
• 154051-85-1 5-fluoro-2-methoxy-benzyloxybenzene 
• 72955-97-6 5-fluoro-2-methoxy phenol 
• 452-08-4 2-bromo-4-fluoro-1-methoxybenzene 
• 154051-84-0 N-trifluoroacetyl-3-methoxy-4-trimethylacetoxy-6-fluorophenylalanine ethyl ester 
• 141523-19-5 N-Benzoyl-3-(2-fluoro-4-hydroxy-5-methoxyphenyl)alanine 
• 141523-16-2 4-Benzyloxy-2-fluoro-5-hydroxybenzaldehyde 
• 79418-72-7 4-Benzyloxy-2-fluoro-5-methoxybenzaldehyde 
• 100-39-0 benzyl bromide 

Relevant academic research and scientific papers

METHOD FOR THE PRODUCTION OF 18F-FLUORINATED ALPHA ACIDS

The invention relates to a method for the production of 18F-fluorinated ?-amino acids and 18F-fluorinated α-amino acid derivatives, comprising the following steps: (a) reaction of a 18F-fluorinated compound of formula I, w

SYNTHESIS AND HPLC SEPARATION OF 6-FLUORO-L-DOPA METABOLITES

The synthesis of 6-fluoro-L-dopa metabolites (3-O-methyl-6-fluorodopa (1b), 6-fluorodopamine (2a), 3-O-methyl-6-fluorodopamine (2b), 3,4-dihydroxy-6-fluorophenylacetic acid (3a) and 6-fluorohomovanillic acid (3b) is described.A HPLC method for their separ

Synthesis of metabolites of 6-fluoro-DOPA

Key metabolites of 6-fluoro-DOPA have been prepared by side-chain elaboration of 6-fluorovanillin and 6-fluoroveratraldehyde.