344414-08-0

Basic information

• Product Name: N-tert-butoxycarbonyl-[N-2(N²-acetyl-O⁶-p-nitrophenylethylguanine-9-yl)ethyl]glycine methyl ether
• CAS NO: 344414-08-0
• Molecular Weight: 557.563
• Mol File: 344414-08-0.mol

Chemical Properties

• CAS DataBase Reference: N-tert-butoxycarbonyl-[N-2(N²-acetyl-O⁶-p-nitrophenylethylguanine-9-yl)ethyl]glycine methyl ether(CAS DataBase Reference)
• NIST Chemistry Reference: N-tert-butoxycarbonyl-[N-2(N²-acetyl-O⁶-p-nitrophenylethylguanine-9-yl)ethyl]glycine methyl ether(344414-08-0)
• EPA Substance Registry System: N-tert-butoxycarbonyl-[N-2(N²-acetyl-O⁶-p-nitrophenylethylguanine-9-yl)ethyl]glycine methyl ether(344414-08-0)

Safety Data

• Hazardous Substances Data: 344414-08-0(Hazardous Substances Data)

Upstream product

• 3056-33-5 2,9-diacetylguanine 
• 100-27-6 2-(4-nitrophenyl)ethanol 
• 189160-68-7 N-tert-Butoxycarbonyl-N-(2-hydroxyethyl)glycine methyl ester 
• 218152-30-8 N²-acetyl-O⁶-(2-(p-nitrophenyl)ethyl)guanine 

Relevant articles and documents

Synthesis of N-Boc and N-Fmoc dipeptoids with nucleobase residues as peptoid nucleic acid monomers

The synthesis of Boc and Fmoc protected peptoid nucleic acid monomers bearing thymine (4a, 4b), adenine (6a, 6b) or guanine (7a, 7b) on the side chain is described. These nucleobases were attached to the amino group of glycine via an ethylene linkage using the Mitsunobu reaction, except cytosine, which was attached using alkylation. After deprotection, these amino acids have been used for synthesizing N-Boc and N-Fmoc dipeptoids.