65391-10-8

Basic information

• Product Name: N-phthalimido-D,L-serine
• Synonyms: N-phthalimido-D,L-serine
• CAS NO: 65391-10-8
• Molecular Weight: 235.196
• Mol File: 65391-10-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N-phthalimido-D,L-serine(CAS DataBase Reference)
• NIST Chemistry Reference: N-phthalimido-D,L-serine(65391-10-8)
• EPA Substance Registry System: N-phthalimido-D,L-serine(65391-10-8)

Safety Data

• Hazardous Substances Data: 65391-10-8(Hazardous Substances Data)

Upstream product

• 85-44-9 phthalic anhydride 
• 302-84-1 serin 

Downstream Products

• 550-44-7 N-methylphthalimide 
• 3485-84-5 N-vinylphthalimide 
• 3891-07-4 N-(2-Hydroxyethyl)phthalimide 
• 127756-70-1 trans-4-benzoyloxy-1-(4-methoxyphenyl)-3-phthalimidoazetidin-2-one 
• 127756-75-6 trans-4-(2-bromoethoxy)-1-(4-methoxyphenyl)-3-phthalimidoazetidin-2-one 
• 115933-61-4 benzyl 3-bromo-2-phtalimidopropionohydroxamate 
• 115957-18-1 3-bromo-N-(4-methoxyphenyl)-2-phtalimidopropionamide 
• 115957-20-5 1-(4-methoxyphenyl)-3-phthalimidoazetidin-2-one 
• 68749-65-5 (4-Benzyloxy-phenyl)-[3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-2-oxo-azetidin-1-yl]-acetic acid methyl ester 
• 68749-66-6 [3-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-2-oxo-azetidin-1-yl]-(4-hydroxy-phenyl)-acetic acid methyl ester 
• 152402-70-5 N-(tosyloxy)-3-phthalimido-2-azetidinone 
• 115933-62-5 O-benzyl-N-hydroxy-3-phthalimido-2-azetidinone 
• 124998-12-5 2-(2-{3,5-Dioxo-4-[5-oxo-5H-furan-(2E)-ylidene]-2-phenyl-pyrazolidin-1-yl}-1-hydroxymethyl-2-oxo-ethyl)-isoindole-1,3-dione 
• 124998-09-0 2-(2-{4-[1-Amino-meth-(E)-ylidene]-3,5-dioxo-2-phenyl-pyrazolidin-1-yl}-1-hydroxymethyl-2-oxo-ethyl)-isoindole-1,3-dione 

Relevant articles and documents

Synthesis and study of modified polyvinyl alcohol containing amino acid moieties as anticancer agent

A series of new phthalimides compounds[3-7]a-i were synthesized from reaction of Malic anhydride, phthalic anhydride, nitro phthalic anhydride, 2-phenyl-4H-benzo[d][1,3]oxazin-4-one, 2-(4-nitrophenyl)-4H-benzo[d][1,3]oxazin-4-one with different amino acids as glycine, alanine, valine, leucine, isoleucine, serine, threonine, tyrosine and Phenyl alanine [1]a-i under fusion conditions. Compounds [3-7]a-i react with SOCl2 in the presence of benzene to produce compounds [8-12]a-i. Chemical modification of Poly(vinyl alcohol)were obtained by reaction of PVA with compounds [8-12]a-i using the dimethyl formamide to give compounds [13-17]a-i. The structure of the synthesized compounds was characterized by their analytical and spectral data as, IR spectra, 1H, 13C-NMR, Elemental analysis (CHN), UV-Vis Spectroscopy, Scanning electron microscopy (SEM), Antibacterial activity were screened via two kinds of bacteria. Also, anticancer activity were examined for most of the modified polyvinyl alcohol.