177738-46-4

Upstream product

• 25905-50-4 5’-chloro-5’-deoxythymidine 
• 263746-51-6 4,4'-dimethoxytriphenylmethanethiol 
• 29391-35-3 ((2R,3S,5R)-3-hydroxy-5-(5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1 (2H)-yl)tetrahydrofuran-2-yl)methyl methanesulfonate 
• 7253-19-2 5'-O-(p-toluenesulfonyl)thymidine 
• 40615-36-9 4,4'-dimethoxytrityl chloride 
• 7150-83-6 5'-thio-thymidine 
• 40615-35-8 4,4'-dimethoxytrityl alcohol 
• 144944-94-5 5'-S-acetyl-5'-deoxy-5'-thiothymidine 
• 50-89-5 thymidine 

Downstream Products

• 500775-64-4 5'-S-(4,4'-dimethoxytrityl)-5'-thiothymidine 3'-(2-cyanoethyl-diisopropylphosphoramidite) 

Relevant academic research and scientific papers

Efficient solid phase synthesis of cleavable oligodeoxynucleotides based on a novel strategy for the synthesis of 5′-S-(4,4′-dimethoxytrityl)- 2′-deoxy-5′-thionucleoside phosphoramidites

The incorporation of a specific cleavage site into an oligodeoxynucleotide can be achieved by utilizing the four 5′-S-(4,4′-dimethoxytrityl)- 2′-deoxy-5′-thionucleoside 3′-(2-cyanoethyl diisopropylphosphoramidites) 5 and 15a-c (Fig.1). Based on the silver

A new concept for DNA-arrays

We will insert a cleavage site in an oligodeoxynucleotide, which can be used for a selective and quantitative cleavage. For that reason we synthesized the four 5′-S-(4,4′-dimethoxytrityl)-mercapto-2′ -deoxynucleotide-3′-O-(2-cyanoethoxydiisopropylamino)-p