179472-13-0

Basic information

• Product Name: 2-[(tert-butyloxycarbonyl)amino]-3-[N₃-benzoyl(thymin-1-yl)]-L-propan-1-ol
• Synonyms: 2-[(tert-butyloxycarbonyl)amino]-3-[N₃-benzoyl(thymin-1-yl)]-L-propan-1-ol
• CAS NO: 179472-13-0
• Molecular Weight: 403.435
• Mol File: 179472-13-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-[(tert-butyloxycarbonyl)amino]-3-[N₃-benzoyl(thymin-1-yl)]-L-propan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[(tert-butyloxycarbonyl)amino]-3-[N₃-benzoyl(thymin-1-yl)]-L-propan-1-ol(179472-13-0)
• EPA Substance Registry System: 2-[(tert-butyloxycarbonyl)amino]-3-[N₃-benzoyl(thymin-1-yl)]-L-propan-1-ol(179472-13-0)

Safety Data

• Hazardous Substances Data: 179472-13-0(Hazardous Substances Data)

Upstream product

• 469886-48-4 (2S)-[1-(tert-butyldiphenylsilanyloxymethyl)-2-hydroxyethyl]carbamic acid tert-butyl ester 
• 2766-43-0 N-tert-butyloxycarbonyl-L-serine methyl ester 
• 126645-26-9 (S)-methyl 2-((tert-butoxycarbonyl)amino)-3-((tert-butyldimethylsilyl)oxy)propanoate 
• 152491-85-5 (R)-[1-(tert-butyl-dimethyl-silanyloxymethyl)-2-hydroxy-ethyl]-carbamic acid tert-butyl ester 
• 66866-45-3 C₂₀H₂₉NO₇ 
• 79069-15-1 N-(tert-butyloxycarbonyl)-O-benzyl-L-serinol 
• 23680-31-1 BOC-O-benzyl-L-serine 
• 24424-99-5 di-tert-butyl dicarbonate 
• 179472-12-9 1-O-benzyl-2-[(tert-butyloxycarbonyl)amino]-3-[N₃-benzoyl(thymin-1-yl)]-L-propanol 
• 4330-20-5 N-3-benzoylthymine 

Downstream Products

• 179472-16-3 1-O-isobutyryl-2-[[β-(4,4'-dimethoxytrityl)-O-acetyl]amino]-3-[N3-benzoyl(thymin-1-yl)]-L-propanol 
• 179472-17-4 2-[[β-(4,4'-dimethoxytrityl)-O-acetyl]amino]-3-(thymin-1-yl)-L-propanol 
• 179472-15-2 1-O-isobutyryl-2-[(β-hydroxyacetyl)amino]-3-[N3-benzoyl(thymin-1-yl)]-L-propanol 
• 179472-14-1 1-O-isobutyryl-2-[(tert-butyloxycarbonyl)amino]-3-[N₃-benzoyl(thymin-1-yl)]-L-propanol 

Relevant articles and documents

Simple molecular engineering of glycol nucleic acid: Progression from self-pairing to cross-pairing with cDNA and RNA

The acyclic chiral nucleic acid analogue, Glycol Nucleic Acid (GNA), displayed exceptional structural simplicity and atom economy while forming self-paired duplexes, using canonical Watson-Crick base pairing. We disclose here that the replacement of phosp