36913-17-4

Basic information

• Product Name: 3'-Deoxy-N,N-dimethyl-3'-(benzylamino)adenosine
• Synonyms: 3'-Deoxy-N,N-dimethyl-3'-(benzylamino)adenosine
• CAS NO: 36913-17-4
• Molecular Formula: C₁₉H₂₄N₆O₃
• Molecular Weight: 384.43226
• Mol File: 36913-17-4.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3'-Deoxy-N,N-dimethyl-3'-(benzylamino)adenosine(CAS DataBase Reference)
• NIST Chemistry Reference: 3'-Deoxy-N,N-dimethyl-3'-(benzylamino)adenosine(36913-17-4)
• EPA Substance Registry System: 3'-Deoxy-N,N-dimethyl-3'-(benzylamino)adenosine(36913-17-4)

Safety Data

• Hazardous Substances Data: 36913-17-4(Hazardous Substances Data)

Upstream product

• 934011-54-8 9-[3-(benzylamino)-3-N,2-O-carbonyl-3-deoxy-β-D-ribofuranosyl]-N⁶,N⁶-dimethyladenine 
• 934011-52-6 9-[2-O-(N-benzylcarbamoyl)-3,5-O-sulfinyl-β-D-xylofuranosyl]-N⁶,N⁶-dimethyladenine 
• 669055-52-1 9-(β-D-xylofuranosyl)-N⁶,N⁶-dimethyladenine 
• 669055-54-3 9-(3,5-O-sulfinyl-β-D-xylofuranosyl)-N⁶,N⁶-dimethyladenine 

Downstream Products

• 58-60-6 3'-amino-3'-deoxy-N⁶,N⁶-dimethyladenosine 

Relevant articles and documents

A simple and efficient synthesis of puromycin, 2,2′-anhydro- pyrimidine nucleosides, cytidines and 2′,3′-anhydroadenosine from 3′,5′-O-sulfinyl xylo-nucleosides

Synthesis of antibiotics, puromycin and 3 ′-amino-3 ′-deoxy-N 6 ,N 6 -dimethyladenosine 11 was achieved by utilizing the cyclic sulfite 6a of the xylo -3 ′,5 ′-dihydroxy group as a new protective group. The key synthetic step is the deprotection of the sulfite moiety through the intramolecular cyclization of 2-α-carbamate 7 . In a similar manner, 2,2 ′-anhydro-pyrimidine nucleosides 15 , ribo -cytidines 17 and 2 ′,3 ′-anhydroadenosine 14 were prepared in high yields from the corresponding sulfites 4 , 5 , and 6b , respectively. Copyright Taylor & Francis Group, LLC.