109063-69-6

Basic information

• Product Name: (S)-methyl 2-amino-3-(naphthalen-2-yl)propanoate
• Synonyms: (S)-methyl 2-amino-3-(naphthalen-2-yl)propanoate
• CAS NO: 109063-69-6
• Molecular Weight: 229.279
• Mol File: 109063-69-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-methyl 2-amino-3-(naphthalen-2-yl)propanoate(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-methyl 2-amino-3-(naphthalen-2-yl)propanoate(109063-69-6)
• EPA Substance Registry System: (S)-methyl 2-amino-3-(naphthalen-2-yl)propanoate(109063-69-6)

Safety Data

• Hazardous Substances Data: 109063-69-6(Hazardous Substances Data)

Downstream Products

• 1065276-58-5 methyl (S)-3-(naphthalen-2-yl)-2-((S)-2-(2-nitrophenylsulfonamido)pentanamido)propanoate 
• 686338-00-1 3-naphthalen-2-yl-2-[2-(2-nitro-benzenesulfonylamino)-butyryl-amino]-propionic acid methyl ester 
• 1065276-59-6 C₂₃H₂₃N₃O₇S 
• 1065276-60-9 C₂₅H₂₇N₃O₇S 
• 1609554-63-3 tert-butyl (2S)-3-(4-(allyloxy)phenyl)-2-((2S)-2-((2S,4S)-4-azido-1-((2S)-2-((2S)-2-((tert-butoxycarbonyl)(methyl)amino)propanamido)-3,3-dimethylbutanoyl)pyrrolidine-2-carboxamido)-3-(naphthalen-2-yl)propanamido)propanoate 
• 1207726-19-9 C₂₇H₂₅NO₅ 
• 1207726-20-2 C₂₅H₂₃N₃O₃ 
• 181646-03-7 (R)-2-(3-(tert-Butoxycarbonylaminomethyl)benzoylamino)-3-(2-naphthyl)-propionic acid methyl ester 
• 202811-56-1 (2R)-2-(2-naphthyl)methyl-3-oxo-4-phenethylpiperazine-1-carboxylic acid tert-butyl ester 
• 894407-01-3 (3S,4S)-4-{N-[4-(tert-butoxycarbonylamino)butyl]-N-(2-nitrobenzenesulfonyl)}amino-3-[(tert-butyl)dimethylsiloxy]-5-(2-naphthyl)pent-1-ene 
• 894407-04-6 (5S,6S)-1-[4-(tert-butoxycarbonylamino)butyl]-5,6-dihydro-5-diphenylphosphoryloxy-6-[(2-naphthyl)methyl]pyridin-2-one 
• 894407-00-2 (3S,4S)-3-[(tert-butyl)dimethylsiloxy]-5-(2-naphthyl)-4-[N-(2-nitrobenzenesulfonyl)amino]pent-1-ene 
• 176896-73-4 methyl (S)-2-[(tert-butoxycarbonyl)amino]-3-(naphthalen-2-yl)propanoate 

Relevant articles and documents

Molecular interaction sites of interleukin-2 RNA and methods of modulating the same

Methods for the identification of compounds which modulate, either inhibit or stimulate, biomolecules are provided. Nucleic acids, especially RNAs are preferred substrates for such modulation. The present methods are particularly powerful in that they provide novel combinations of techniques which give rise to compounds, usually “small” organic compounds, which are highly potent modulators of RNA and other biomolecular activity. In accordance with preferred aspects of the invention, very large numbers of compounds may be tested essentially simultaneously to determine whether they are likely to interact with a molecular interaction site and modulate the activity of the biomolecule. Pharmaceuticals, veterinary drugs, agricultural chemicals, industrial chemicals, research chemicals and many other beneficial compounds may be identified in accordance with embodiments of this invention.