519141-03-8

Basic information

• Product Name: 1-methyl-3-benzyloxycarbonylpiperazine-2,5-dione
• Synonyms: 1-methyl-3-benzyloxycarbonylpiperazine-2,5-dione
• CAS NO: 519141-03-8
• Molecular Weight: 262.265
• Mol File: 519141-03-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1-methyl-3-benzyloxycarbonylpiperazine-2,5-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 1-methyl-3-benzyloxycarbonylpiperazine-2,5-dione(519141-03-8)
• EPA Substance Registry System: 1-methyl-3-benzyloxycarbonylpiperazine-2,5-dione(519141-03-8)

Safety Data

• Hazardous Substances Data: 519141-03-8(Hazardous Substances Data)

Upstream product

• 31661-15-1 dibenzyl aminomalonate 
• 865879-17-0 benzyl N-[N-t-butoxycarbonylsarcosyl]-2-benzyloxycarbonylglycinate 
• 51118-40-2 dibenzyl 2-(hydroxyimino)malonate 
• 15014-25-2 malonic acid dibenzyl ester 

Downstream Products

• 519141-15-2 3-benzyl-3-benzyloxycarbonyl-1,4-dimethylpiperazine-2,5-dione 
• 519141-07-2 9a-benzyloxycarbonyl-2-methyl-1,4-dioxo-1,2,3,4,6,9-hexahydropyrido[1,2-a]pyrazine 
• 519141-14-1 3-benzyloxycarbonyl-1,3,4-trimethylpiperazine-2,5-dione 
• 519141-25-4 2-benzyl-1,4-dimethyl-3,6-dioxo-piperazine-2-carboxylic acid 
• 519141-20-9 3-acetoxy-2-benzyl-1,4-dimethylpiperazine-2,5-dione 
• 519141-18-5 3-methoxy-1,3,4-trimethylpiperazine-2,5-dione 
• 59552-45-3 (Z)-3-benzylidene-1,4-dimethylpiperazine-2,5-dione 
• 182067-63-6 1,3,4-trimethylpiperazine-2,5-dione 
• 5076-82-4 sarcosine anhydride 
• 519141-04-9 3-benzyloxycarbonyl-1,4-dimethylpiperazine-2,5-dione 
• 519141-16-3 4-acetyl-3-benzyloxycarbonyl-1-methylpiperazine-2,5-dione 
• 519141-06-1 3,4-diallyl-3-benzyloxycarbonyl-1-methylpiperazine-2,5-dione 
• 198877-45-1 1,4-dimethyl-3-methylenepiperazine-2,5-dione 
• 5616-94-4 2-methyl-hexahydropyrrolo[1,2-a]pyrazine-1,4-dione 

Relevant articles and documents

Multi-purpose functionality for the structural elaboration of the piperazine-2,5-dione motif

Mild methods for controlled C- and N-alkylation of 3-benzyloxycarbonylpiperazine-2,5-diones are reported. The benzyloxylcarbonyl substituent can also serve as latent functionality for N-acyliminium ion formation and subsequent trapping enables installation of new carbon and/or heteroatom substituents.