191655-63-7

Basic information

• Product Name: tert-butyl 7-(N³-benzoylthymin-1-yl)-5S-[N-(tert-butoxycarbonyl)amino]-3-oxaheptanate
• Synonyms: tert-butyl 7-(N³-benzoylthymin-1-yl)-5S-[N-(tert-butoxycarbonyl)amino]-3-oxaheptanate
• CAS NO: 191655-63-7
• Molecular Weight: 531.606
• Mol File: 191655-63-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: tert-butyl 7-(N³-benzoylthymin-1-yl)-5S-[N-(tert-butoxycarbonyl)amino]-3-oxaheptanate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl 7-(N³-benzoylthymin-1-yl)-5S-[N-(tert-butoxycarbonyl)amino]-3-oxaheptanate(191655-63-7)
• EPA Substance Registry System: tert-butyl 7-(N³-benzoylthymin-1-yl)-5S-[N-(tert-butoxycarbonyl)amino]-3-oxaheptanate(191655-63-7)

Safety Data

• Hazardous Substances Data: 191655-63-7(Hazardous Substances Data)

Upstream product

• 4330-20-5 N-3-benzoylthymine 
• 220418-65-5 tert-butyl 7-hydroxy-5S-[N-(tert-butoxycarbonyl)amino]-3-oxaheptanate 
• 191655-44-4 (2S)-2-tert-butoxycarbonylamino-4-(tert-butyldimethyl-silanyloxy)-butyric acid benzyl ester 
• 220418-64-4 [2-tert-butoxycarbonylamino-4-(tetrahydro-pyran-2-yloxy)-butoxy]-acetic acid tert-butyl ester 
• 147325-09-5 N-Boc-L-homoserine ethyl ester 
• 24424-99-5 di-tert-butyl dicarbonate 
• 5292-43-3 bromoacetic acid tert-butyl ester 
• 191655-45-5 (2S)‐2‐{[(tert‐butoxy)carbonyl]amino}‐4‐[(tert‐butyldimethylsilyl)oxy]butanoic acid 
• 191655-46-6 tert-butyl (S)-(4-((tert-butyldimethylsilyl)oxy)-1-hydroxybutan-2-yl)carbamate 
• 105183-60-6 (S)-benzyl 2-((tert-butoxycarbonyl)amino)-4-hydroxybutanoate 
• 220418-62-2 2-tert-butoxycarbonylamino-4-(tetrahydro-pyran-2-yloxy)-butyric acid ethyl ester 
• 220418-63-3 [1-hydroxymethyl-3-(tetrahydro-pyran-2-yloxy)-propyl]-carbamic acid tert-butyl ester 

Relevant articles and documents

Synthesis of δ-amino acids with an ether linkage in the main chain and nucleobases on the side chain as monomer units for oxy-peptide nucleic acids

Syntheses of four N-Fmoc δ-amino acids with an ether linkage in the main chain and four different nucleobases on the side chain, Fmoc-NH- C*H(CH2-CH2-B)-CH2-O-CH2-COOH (B=thymine, uracil, N4-benzoylcytosine, and N2-isobutyrylguanine) are described. The δ-amino acids were prepared through 8-12 step synthesis starting from L-homoserine and could be linked together to form novel peptide nucleic acids (oxy-PNAs = OPNAs).