39740-33-5

Basic information

• Product Name: carboxymethyl-1 N-acetyl-2 (dihydroxy-3,4 phenyl)-3 alanine
• Synonyms: carboxymethyl-1 N-acetyl-2 (dihydroxy-3,4 phenyl)-3 alanine
• CAS NO: 39740-33-5
• Molecular Weight: 253.255
• Mol File: 39740-33-5.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: carboxymethyl-1 N-acetyl-2 (dihydroxy-3,4 phenyl)-3 alanine(CAS DataBase Reference)
• NIST Chemistry Reference: carboxymethyl-1 N-acetyl-2 (dihydroxy-3,4 phenyl)-3 alanine(39740-33-5)
• EPA Substance Registry System: carboxymethyl-1 N-acetyl-2 (dihydroxy-3,4 phenyl)-3 alanine(39740-33-5)

Safety Data

• Hazardous Substances Data: 39740-33-5(Hazardous Substances Data)

Upstream product

• 59-92-7 levodopa 
• 7101-51-1 L-DOPA methyl ester 
• 108-24-7 acetic anhydride 
• 106787-98-8 (S)-N-methylthiocarbonyl-3,4-dihydroxyphenylalanine methyl ester 
• 67-56-1 methanol 
• 47302-76-1 N-acetyl-2 (di-O-acetyl-3,4 phenyl)-3 alanine 
• 106787-68-2 (S)-3-(3,4-Diacetoxy-phenyl)-2-thioacetylamino-propionic acid methyl ester 
• 1421-65-4 L-dopa methyl ester hydrochloride 
• 105760-25-6 N,O,O'-triacetyl-3,4-dihydroxyphenylalanine methyl ester 

Downstream Products

• 78148-21-7 methyl (S)-2-acetamido-3-(3,4-dimethoxyphenyl)propanoate 
• 79439-71-7 carboxymethyl-1 N-acetyl-2 -3 alanine 
• 79439-73-9 carboxymethyl-1 N-acetyl-2 -3 alanine 
• 6988-74-5 N-acetyl tri-O-benzoyl-2,3,5-D-ribofuranosylamine 
• 14215-97-5 1-O-acetyl-2,3,5-tri-O-benzoyl-D-ribofuranose 

Relevant articles and documents

Easy access to drug building-blocks through benzylic C-H functionalization of phenolic ethers by photoredox catalysis

A visible light-mediated photocatalyzed C-C-bond forming method for the benzylic C-H functionalization of phenolether containing synthetic building blocks based on a radical-cation/deprotonation strategy is reported. This method allows the mild, selective generation of benzyl radicals in phenolic complex molecules and drug-like compounds, providing new entries in synthetic and medicinal chemistry.

Process for producing threo-3-(3,4-dihydroxyphenyl)serine

Racemic or optically active threo-3-(3,4-dihydroxyphenyl)serine can be readily produced via a few short steps by a process involving the steps of reacting a racemic or optically active N-acyl DOPA derivative represented by the formula ?I!: STR1 wherein X

L-αmethyldopa and L-dopa ribosides and derivatives

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