312613-63-1

Basic information

• Product Name: benzyl N-[2-(tert-butoxycarbonyl)aminoethyl]-N-[[2-N-(isobutyryl)guanin-9-yl]acetyl]glycinate
• Synonyms: benzyl N-[2-(tert-butoxycarbonyl)aminoethyl]-N-[[2-N-(isobutyryl)guanin-9-yl]acetyl]glycinate
• CAS NO: 312613-63-1
• Molecular Weight: 569.618
• Mol File: 312613-63-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: benzyl N-[2-(tert-butoxycarbonyl)aminoethyl]-N-[[2-N-(isobutyryl)guanin-9-yl]acetyl]glycinate(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl N-[2-(tert-butoxycarbonyl)aminoethyl]-N-[[2-N-(isobutyryl)guanin-9-yl]acetyl]glycinate(312613-63-1)
• EPA Substance Registry System: benzyl N-[2-(tert-butoxycarbonyl)aminoethyl]-N-[[2-N-(isobutyryl)guanin-9-yl]acetyl]glycinate(312613-63-1)

Safety Data

• Hazardous Substances Data: 312613-63-1(Hazardous Substances Data)

Upstream product

• 121505-93-9 tert-butyl N-{[methoxy(methyl)carbamoyl]methyl}carbamate 
• 2462-31-9 benzyl 2-aminoacetate hydrochloride 
• 89711-08-0 N-(t-butoxycarbonyl)glycinal 
• 4530-20-5 BOC-glycine 
• 172405-20-8 2-(2-isobutyramido-6-oxo-1H-purin-9(6H)-yl)acetic acid 
• 158663-62-8 N-((tert-butoxycarbonyl)-aminoethyl)glycine benzyl ester 

Relevant articles and documents

PNA-DNA duplexes, triplexes, and quadruplexes are stabilized with trans-cyclopentane units

Peptide nucleic acids (PNAs) are non-natural nucleic acid mimics that bind to complementary DNA and RNA with high affinity and selectivity. PNA can bind to nucleic acids in a number of different ways. Currently, the formation of PNA-oligonucleotide duplex, triplex, and quadruplex structures have been reported. PNAs have been used in numerous biomedicial applications, but there are few strategies to predictably improve the binding properties of PNAs by backbone modification. We have been studying the benefits of incorporating (S,S)-trans-cyclopentane diamine units (tcyp) into the PNA backbone. In this Communication, we report the improvement in stability associated with tcyp incorporation into PNA-DNA duplexes, triplexes, and quadruplexes. The broad utility of this modification across multiple types of PNA structures is unique and should prove useful in the development of applications that rely on PNA. Copyright