71508-05-9

Basic information

• Product Name: Adenosine, 3'-[[(2S)-2-amino-3-(4-methoxyphenyl)-1-oxopropyl]amino]-3'-deoxy-
• CAS NO: 71508-05-9
• Molecular Formula: C20H25N7O5
• Molecular Weight: 443.462
• Mol File: 71508-05-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Adenosine, 3'-[[(2S)-2-amino-3-(4-methoxyphenyl)-1-oxopropyl]amino]-3'-deoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Adenosine, 3'-[[(2S)-2-amino-3-(4-methoxyphenyl)-1-oxopropyl]amino]-3'-deoxy-(71508-05-9)
• EPA Substance Registry System: Adenosine, 3'-[[(2S)-2-amino-3-(4-methoxyphenyl)-1-oxopropyl]amino]-3'-deoxy-(71508-05-9)

Safety Data

• Hazardous Substances Data: 71508-05-9(Hazardous Substances Data)

Upstream product

• 1273196-83-0 9-[3-bromo-5-O-tert-butyldiphenylsilyl-3-deoxy-2-O-(N-vinylcarbamoyl)-β-D-xylofuranosyl]adenine 
• 1273196-85-2 C₂₉H₃₂N₆O₄Si 
• 1273196-87-4 3'-amino-5'-O-(tert-butyldiphenylsilyl)-3-deoxyadenosine 
• 1273196-89-6 5'-O-(tert-butyldiphenylsilyl)-3'-[N-(9-fluorenyl)methoxycarbonyl-O-methyl-L-tyrosyl]amido-3'-deoxyadenosine 
• 2627-64-7 9-(2,3-anhydro-β-D-ribofuranosyl)adenine 
• 125084-70-0 9-<2,3-anhydro-5-O-<(tert-butyl)diphenylsilyl>-β-D-ribofuranosyl>adenine 
• 125084-68-6 9-<3-bromo-5-O-<(tert-butyl)diphenylsilyl>-3-deoxy-β-D-xylofuranosyl>adenine 
• 58-61-7 adenosine 
• 118525-25-0 9-[2',5'-bis-(O-tert-butyldimethylsilyl)-β-D-xylofuranosyl]-9H-adenine 
• 86734-95-4 9-(2,5-di-O-tert-butyldimethylsilyl-β-D-erythro-pentofuran-3-ulosyl)adenosine 
• 65109-11-7 2',5'-bis-O-(tert-butyldimethylsilyl)adenosine 
• 77128-72-4 N-(9-fluorenylmethoxycarbonyl)-O-methyl-L-tyrosine 

Relevant articles and documents

Shorter puromycin analog synthesis by means of an efficient Staudinger-Vilarrasa coupling

An efficient Staudinger-Vilarrasa coupling generates amides from azides and 1-hydroxybenzotriazole esters of amino- or hydroxy acid derivatives in very high isolated yields and purity. New puromycin analogs, mostly putative biosynthetic intermediates, wer

High-yield immobilization of a puromycin analogue for the solid support synthesis of aminoacyl-tRNA fragments

(Matrix presented) An efficient procedure for the immobilization of 3′-deoxy-3′-(O-methyltyrosyl)aminoadenosine was developed. A poly(ethylene glycol)-derived diacid linker/spacer was attached to aminomethyl polystyrene. Coupling of the 2′-hydroxy instead

Facile and rapid access to inosine puromycin analogues through the use of adenylate deaminase

To study the ribosomal peptidyl transfer, puromycin analogues are of interest in which adenine has been replaced by hypoxanthine. We synthesized inosine puromycin analogues from 3′-azidodeoxyadenosine derivatives using adenylate deaminase for the quantita