140146-47-0

Basic information

• Product Name: 2-(2-fluoro-4-hydroxy-5-methoxyphenyl)acetic acid
• Synonyms: 2-(2-fluoro-4-hydroxy-5-methoxyphenyl)acetic acid
• CAS NO: 140146-47-0
• Molecular Weight: 200.166
• Mol File: 140146-47-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-(2-fluoro-4-hydroxy-5-methoxyphenyl)acetic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-fluoro-4-hydroxy-5-methoxyphenyl)acetic acid(140146-47-0)
• EPA Substance Registry System: 2-(2-fluoro-4-hydroxy-5-methoxyphenyl)acetic acid(140146-47-0)

Safety Data

• Hazardous Substances Data: 140146-47-0(Hazardous Substances Data)

Upstream product

• 141523-16-2 4-Benzyloxy-2-fluoro-5-hydroxybenzaldehyde 
• 79418-72-7 4-Benzyloxy-2-fluoro-5-methoxybenzaldehyde 
• 100-39-0 benzyl bromide 
• 452-08-4 2-bromo-4-fluoro-1-methoxybenzene 
• 154051-92-0 3-methoxy-4-benzyloxy-6-fluorophenylacetic acid 
• 154051-83-9 ethyl 3-methoxy-4-trimethylacetoxy-6-fluorophenylacetate 
• 141523-20-8 (4-Benzyloxy-2-fluoro-5-methoxy-phenyl)-trimethylsilanyloxy-acetonitrile 
• 141523-15-1 2-(2-fluoro-4-hydroxy-5-methoxyphenyl)-2-hydroxyacetic acid 
• 496-69-5 2-bromo-4-fluoro-phenol 
• 72955-97-6 5-fluoro-2-methoxy phenol 
• 60563-13-5 ethyl homovanillate 
• 154051-81-7 ethyl 3-methoxy-4-trimethylacetoxyphenylacetate 
• 154051-86-2 3-methoxy-4-benzyloxy-6-fluorobenzyl chloride 
• 154051-90-8 3-methoxy-4-benzyloxy-6-fluorophenylacetonitrile 

Relevant articles and documents

Phenyl-fluoride substituted phenylacetic acid ester compound and use thereof

The invention relates to a phenyl-fluoride substituted phenylacetate compound shown as a general formula (I), a pharmaceutical composition containing the same and application thereof to anesthesia, sedation and analgesia.

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