340721-55-3

Basic information

• Product Name: N⁶-benzoyl-2'-deoxy-3',5'-bis-O-(triethylsilyl)adenosine
• Synonyms: N⁶-benzoyl-2'-deoxy-3',5'-bis-O-(triethylsilyl)adenosine
• CAS NO: 340721-55-3
• Molecular Weight: 583.878
• Mol File: 340721-55-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N⁶-benzoyl-2'-deoxy-3',5'-bis-O-(triethylsilyl)adenosine(CAS DataBase Reference)
• NIST Chemistry Reference: N⁶-benzoyl-2'-deoxy-3',5'-bis-O-(triethylsilyl)adenosine(340721-55-3)
• EPA Substance Registry System: N⁶-benzoyl-2'-deoxy-3',5'-bis-O-(triethylsilyl)adenosine(340721-55-3)

Safety Data

• Hazardous Substances Data: 340721-55-3(Hazardous Substances Data)

Upstream product

• 994-30-9 triethylsilyl chloride 
• 4546-72-9 N₆-benzoyl-2'-deoxyadenosine 

Downstream Products

• 340721-51-9 N⁶,5-dibenzoyl-2'-deoxy-8-[(4,4'-dimethoxytrityloxy)methyl]adenosine 3'-(2-cyanoethyl diisopropylphosphoramidite) 
• 340721-53-1 N⁶-benzoyl-8-[(benzoyloxy)methyl]-2'-deoxy-5'-O-(4,4'-dimethoxytrityl)adenosine 3'-(2-cyanoethyl disopropylphosphoramidite) 
• 340721-57-5 N⁶-benzoyl-2'-deoxy-8-[(4,4'-dimethoxytrityloxy)methyl]-3',5'-bis-O-(triethylsilyl)adenosine 
• 340721-63-3 N⁶-benzoyl-8-[(benzoyloxy)methyl]-2'-deoxy-5'-O-(4,4'-dimethoxytrityl)adenosine 
• 340721-59-7 N⁶,5-dibenzoyl-2'-deoxy-8-[(4,4'-dimethoxytrityloxy)methyl]adenosine 
• 340721-61-1 N⁶-benzoyl-8-[(benzoyloxy)methyl]-2'-deoxy-3',5'-bis-O-(triethylsilyl)adenosine 
• 340721-58-6 N⁶-benzoyl-2'-deoxy-8-[(4,4'-dimethoxytrityloxy)methyl]adenosine 
• 340721-56-4 N⁶-benzoyl-2'-deoxy-8-(hydroxymethyl)-3',5'-bis-O-(triethylsilyl)adenosine 
• 340721-62-2 N⁶-benzoyl-8-[(benzoyloxy)methyl]-2'-deoxyadenosine 

Relevant articles and documents

Oligonucleotide analogues with a nucleobase-including backbone. Part 5: 2′-deoxy-8-(hydroxymethyl)adenosine- and 2′-deoxy-6-(hydroxymethyl)uridine-derived phosphoramidites: Synthesis and incorporation into 14-mer DNA strands

The pairing propensity of new DNA analogues with a phosphinato group between O-C(3′) and a newly introduced OCH2 group at C(8) and C(6) of 2′-deoxyadenosine and 2′-deoxyuridine, respectively, was evaluated by force-field calculations and Maruze