1293992-22-9

Basic information

• Product Name: N-(tert-butyloxycarbonyl)-3,4-dihydroxy-L-phenylalanine (9-methoxy-(5,6)-benzocoumarin-1-yl)methyl ester
• Synonyms: N-(tert-butyloxycarbonyl)-3,4-dihydroxy-L-phenylalanine (9-methoxy-(5,6)-benzocoumarin-1-yl)methyl ester
• CAS NO: 1293992-22-9
• Molecular Weight: 535.551
• Mol File: 1293992-22-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-(tert-butyloxycarbonyl)-3,4-dihydroxy-L-phenylalanine (9-methoxy-(5,6)-benzocoumarin-1-yl)methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: N-(tert-butyloxycarbonyl)-3,4-dihydroxy-L-phenylalanine (9-methoxy-(5,6)-benzocoumarin-1-yl)methyl ester(1293992-22-9)
• EPA Substance Registry System: N-(tert-butyloxycarbonyl)-3,4-dihydroxy-L-phenylalanine (9-methoxy-(5,6)-benzocoumarin-1-yl)methyl ester(1293992-22-9)

Safety Data

• Hazardous Substances Data: 1293992-22-9(Hazardous Substances Data)

Upstream product

• 861820-84-0 1-chloromethyl-9-methoxy-3-oxo-3H-naphtho[2,1-b]pyran 
• 30033-24-0 (2S)-3-(3,4-dihydroxyphenyl)-2-[(tert-butoxy)carbonylamino]propanoic acid 

Downstream Products

• 1293992-25-2 3,4-dihydroxy-L-phenylalanine (9-methoxy-(5,6)-benzocoumarin-1-yl)methyl ester 
• 59-92-7 levodopa 

Relevant articles and documents

Phototriggering of neuroactive amino acids from 5,6-benzocoumarinyl conjugates

Uncaging of several neuroactive amino acids, namely β-alanine, tyrosine, 3,4-dihydroxyphenylalanine (DOPA) and glutamic acid from the corresponding 5,6-benzocoumarinyl conjugates was carried out by irradiation at different wavelengths and in different solvent systems. The release of the various amino acids was faster in ACN/HEPES buffer mixtures and for the tyrosine conjugate, an increase in the photolysis reaction rates and the quantitative uncaging of the amino acid was associated with increasing water content in the solvent mixture.