931396-35-9

Basic information

• Product Name: 5-{allyloxycarbonylmethyl-[(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-acetyl]-amino}-4-tert-butoxycarbonylamino-pentanoic acid benzyl ester
• Synonyms: 5-{allyloxycarbonylmethyl-[(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-acetyl]-amino}-4-tert-butoxycarbonylamino-pentanoic acid benzyl ester
• CAS NO: 931396-35-9
• Molecular Weight: 586.642
• Mol File: 931396-35-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 5-{allyloxycarbonylmethyl-[(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-acetyl]-amino}-4-tert-butoxycarbonylamino-pentanoic acid benzyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 5-{allyloxycarbonylmethyl-[(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-acetyl]-amino}-4-tert-butoxycarbonylamino-pentanoic acid benzyl ester(931396-35-9)
• EPA Substance Registry System: 5-{allyloxycarbonylmethyl-[(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-acetyl]-amino}-4-tert-butoxycarbonylamino-pentanoic acid benzyl ester(931396-35-9)

Safety Data

• Hazardous Substances Data: 931396-35-9(Hazardous Substances Data)

Upstream product

• 56-86-0 L-glutamic acid 
• 65-71-4 thymin 
• 931396-33-7 5-(allyloxycarbonylmethyl-amino)-4-tert-butoxycarbonylamino-pentanoic acid benzyl ester 
• 100-51-6 benzyl alcohol 
• 124373-83-7 allyl 2-(tert-butoxycarbonylamino)acetate 
• 79069-62-8 benzyl (S)-4-(t-butyloxycarbonylamino)-5-hydroxypentanoate 
• 13574-13-5 Boc-Glu(OBzl)-OH 
• 1676-73-9 L-glutamic acid γ-benzyl ester 
• 59765-55-8 glycine allyl ester 
• 931396-31-5 5-[allyloxycarbonylmethyl-(2-nitro-benzenesulfonyl)-amino]-4-tert-butoxycarbonylamino-pentanoic acid benzyl ester 
• 868837-28-9 allyl 2-(2-nitrophenylsulfonamido)acetate 
• 20924-05-4 thymidyl acetic acid 

Relevant articles and documents

Synthesis of anionic peptide nucleic acid oligomers including γ-carboxyethyl thymine monomers

Synthesis of a modified thymine monomer based on l-Glu, solid phase synthesis of anionic peptide nucleic acid (PNA) oligomers containing the modified monomer and optimization of the deblocking procedure and cleavage conditions of the PNA oligomers from resin are accomplished.