852333-55-2

Basic information

• Product Name: 2'-deoxy-5'-O-(4,4'-dimethoxytrityl)-2'-(methylamino)uridine
• Synonyms: 2'-deoxy-5'-O-(4,4'-dimethoxytrityl)-2'-(methylamino)uridine
• CAS NO: 852333-55-2
• Molecular Weight: 559.619
• Mol File: 852333-55-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2'-deoxy-5'-O-(4,4'-dimethoxytrityl)-2'-(methylamino)uridine(CAS DataBase Reference)
• NIST Chemistry Reference: 2'-deoxy-5'-O-(4,4'-dimethoxytrityl)-2'-(methylamino)uridine(852333-55-2)
• EPA Substance Registry System: 2'-deoxy-5'-O-(4,4'-dimethoxytrityl)-2'-(methylamino)uridine(852333-55-2)

Safety Data

• Hazardous Substances Data: 852333-55-2(Hazardous Substances Data)

Upstream product

• 173170-12-2 2,2'-O-anhydro-1-<5'-O-(4,4'-dimethoxytrityl)-β-D-arabinofuranosyl>uracil 
• 852333-53-0 2,2'-anhydro-3'-O-(N-methylcarbamoyl)-5'-O-(4,4'-dimethoxytrityl)uridine 
• 852333-54-1 N₂',O₃'-carbonyl-2'-deoxy-5'-O-(4,4'-dimethoxytrityl)-2'-(methylamino)uridine 

Downstream Products

• 852333-56-3 2'-(anthraquinon-2-ylcarboxamido)-2'-deoxy-5'-O-(4,4'-dimethoxytrityl)-2'-N-methyluridine 
• 1326643-18-8 C₄₈H₄₁N₃O₇ 
• 801220-52-0 2′-amino-2′-deoxy-2′-N-methyl-2′-N-(pyren-1-ylmethyl)-5′-O-(4,4′-dimethoxytrityl)uridine 
• 1326643-16-6 2'-amino-2'-deoxy-2'-N-methyl-2'-N-(pyren-1-ylcarbonyl)-5'-O-(4,4'-dimethoxytrityl)uridine 
• 1326643-22-4 2'-amino-2'-deoxy-2'-N-methyl-3'-O-(N,N-diisopropylamino-2-cyanoethoxyphosphinyl)-2'-N-(pyren-1-ylcarbonyl)-5'-O-(4,4'-dimethoxytrityl)uridine 
• 1326643-17-7 2'-amino-2'-deoxy-2'-N-methyl-2'-N-(pyren-1-ylmethylcarbonyl)-5'-O-(4,4'-dimethoxytrityl)uridine 
• 1326643-23-5 2'-amino-2'-deoxy-2'-N-methyl-3'-O-(N,N-diisopropylamino-2-cyanoethoxyphosphinyl)-2'-N-(pyren-1-ylmethylcarbonyl)-5'-O-(4,4'-dimethoxytrityl)uridine 

Relevant articles and documents

3′-Immobilized probes with 2′-caps: Synthesis of oligonucleotides with 2′-N-methyl-2′-(anthraquinone carboxamido)uridine residues

(Chemical Equation Presented) A synthesis for oligodeoxynucleotides with a 3′-terminal 2′-N-methyl-2′-acylamido-2′-deoxyuridine residue was developed. Unlike their unmethylated counterparts, these oligodeoxynucleotides can be stably immobilized on aldehyd