139166-81-7

Basic information

• Product Name: Glycine, N-[(3,4-dihydro-5-methyl-2,4-dioxo-1(2H)-pyrimidinyl)acetyl]-N-[2-[[(1,1- dimethylethoxy)carbonyl]amino]ethyl]-, pentafluorophenyl ester
• CAS NO: 139166-81-7
• Molecular Formula: C22H23F5N4O7
• Molecular Weight: 550.439
• Mol File: 139166-81-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Glycine, N-[(3,4-dihydro-5-methyl-2,4-dioxo-1(2H)-pyrimidinyl)acetyl]-N-[2-[[(1,1- dimethylethoxy)carbonyl]amino]ethyl]-, pentafluorophenyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Glycine, N-[(3,4-dihydro-5-methyl-2,4-dioxo-1(2H)-pyrimidinyl)acetyl]-N-[2-[[(1,1- dimethylethoxy)carbonyl]amino]ethyl]-, pentafluorophenyl ester(139166-81-7)
• EPA Substance Registry System: Glycine, N-[(3,4-dihydro-5-methyl-2,4-dioxo-1(2H)-pyrimidinyl)acetyl]-N-[2-[[(1,1- dimethylethoxy)carbonyl]amino]ethyl]-, pentafluorophenyl ester(139166-81-7)

Safety Data

• Hazardous Substances Data: 139166-81-7(Hazardous Substances Data)

Upstream product

• 65-71-4 thymin 
• 134456-94-3 methyl (5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)ethanoate 
• 152774-08-8 methyl N-[2-(Boc-amino)ethyl]-N-(thymin-1-ylacethyl) glycinate 
• 139166-79-3 1-thyminylacetic acid pentafluorophenyl ester 
• 128421-86-3 methyl N-(2-(tert-butyloxycarbonyl)aminoethyl)glycinate 
• 57260-73-8 N-BOC-1,2-diaminoethane 
• 20924-05-4 thymidyl acetic acid 
• 771-61-9 2,3,4,5,6-pentafluorophenol 
• 139166-80-6 N-(2-t-butoxycarbonylaminoethyl)-N-(thymin-1-ylacetyl)glycine 

Downstream Products

• 289684-68-0 {[2-(2-{(2-tert-butoxycarbonylamino-ethyl)-[(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-acetyl]-amino}-acetylamino)-ethyl]-[(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-acetyl]-amino}-acetic acid pentafluorophenyl ester 

Relevant articles and documents

Synthesis and photochemical behavior of peptide nucleic acid dimers and analogues containing 4-thiothymine: Unprecedented (5-4) photoadduct reversion

Pna dimers 1, 5, containing either 4-thiothymine or N3-methyl- 4-thiothymine, were prepared, and the crystal structure of compound 3 was established. With regard to their photochemistry none of these PNA analogues were able to fully mimic the p

Peptide Nucleic Acids (PNA). Oligonucleotide Analogues with an Achiral Peptide Backbone

-