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N6-(1-nitropyren-6-yl)-3'-O-(tetrahydrofuranyl)-5'-O-trityldeoxyadenosine

Base Information
  • Chemical Name:N6-(1-nitropyren-6-yl)-3'-O-(tetrahydrofuranyl)-5'-O-trityldeoxyadenosine
  • CAS No.:163631-85-4
  • Molecular Formula:C49H40N6O6
  • Molecular Weight:808.893
  • Hs Code.:
N<sup>6</sup>-(1-nitropyren-6-yl)-3'-O-(tetrahydrofuranyl)-5'-O-trityldeoxyadenosine

Synonyms:N6-(1-nitropyren-6-yl)-3'-O-(tetrahydrofuranyl)-5'-O-trityldeoxyadenosine

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Chemical Property of N6-(1-nitropyren-6-yl)-3'-O-(tetrahydrofuranyl)-5'-O-trityldeoxyadenosine
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Technology Process of N6-(1-nitropyren-6-yl)-3'-O-(tetrahydrofuranyl)-5'-O-trityldeoxyadenosine

There total 3 articles about N6-(1-nitropyren-6-yl)-3'-O-(tetrahydrofuranyl)-5'-O-trityldeoxyadenosine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
Multi-step reaction with 3 steps
1.1: HBF4; NaNO2 / acetonitrile; H2O
1.2: 18 percent / 160 °C
2.1: HNO3 / acetic acid / 0.5 h / 20 °C
3.1: 31 percent / K2CO3 / dimethylsulfoxide / 24 h / 140 °C
With tetrafluoroboric acid; nitric acid; potassium carbonate; sodium nitrite; In water; acetic acid; dimethyl sulfoxide; acetonitrile; 1.1: Diazotization / 1.2: Decomposition / 2.1: Nitration / 3.1: Addition;
DOI:10.1021/tx00047a009
Guidance literature:
Multi-step reaction with 2 steps
1: HNO3 / acetic acid / 0.5 h / 20 °C
2: 31 percent / K2CO3 / dimethylsulfoxide / 24 h / 140 °C
With nitric acid; potassium carbonate; In acetic acid; dimethyl sulfoxide; 1: Nitration / 2: Addition;
DOI:10.1021/tx00047a009
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