C₂₀H₂₃IN₆O₄

Base Information

Chemical Name:C₂₀H₂₃IN₆O₄
CAS No.:1315073-28-9
Molecular Formula:C₂₀H₂₃IN₆O₄
Molecular Weight:538.345
Hs Code.:

C<sub>20</sub>H<sub>23</sub>IN<sub>6</sub>O<sub>4</sub>

Synonyms:C₂₀H₂₃IN₆O₄

Suppliers and Price of C₂₀H₂₃IN₆O₄

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of C₂₀H₂₃IN₆O₄

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₂₀H₂₃IN₆O₄

There total 10 articles about C₂₀H₂₃IN₆O₄ 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:

Reference yield: 90.0%

: 1315073-26-7
C₂₃H₂₇IN₆O₄

: 1315073-28-9
C₂₀H₂₃IN₆O₄

Guidance literature:: With hydrogenchloride; water; In tetrahydrofuran; at 20 ℃; for 12h;
DOI:10.5012/bkcs.2011.32.5.1620

Reference yield:

: 1315073-20-1
6-chloro-(2,3,5-tribenzoyl-β-D-ribofuranosyl-9-ylmethyl)purine

: 1315073-28-9
C₂₀H₂₃IN₆O₄

Guidance literature:: Multi-step reaction with 6 steps

1.1: triethylamine / ethanol / 20 °C

2.1: sodium methylate / methanol / 1 h / 20 °C

3.1: toluene-4-sulfonic acid / acetone / 0 - 20 °C

3.2: 0.5 h / 20 °C

4.1: dipyridinium dichromate / N,N-dimethyl-formamide / 20 h / 20 °C

5.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / dichloromethane / 12 h / 20 °C

6.1: hydrogenchloride; water / tetrahydrofuran / 12 h / 20 °C

With hydrogenchloride; dipyridinium dichromate; water; sodium methylate; benzotriazol-1-ol; toluene-4-sulfonic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol; ethanol; dichloromethane; N,N-dimethyl-formamide; acetone;
DOI:10.5012/bkcs.2011.32.5.1620

Reference yield:

: 6974-32-9
1-O-acetyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose

: 1315073-28-9
C₂₀H₂₃IN₆O₄

Guidance literature:: Multi-step reaction with 9 steps

1.1: dicobalt octacarbonyl / 0.17 h / 20 °C / 760.05 Torr

1.2: 15 h / 30 °C / 760.05 Torr

2.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 1 h / 0 - 20 °C

3.1: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 0.5 h / 0 °C / Inert atmosphere

3.2: 12 h / 20 °C

4.1: triethylamine / ethanol / 20 °C

5.1: sodium methylate / methanol / 1 h / 20 °C

6.1: toluene-4-sulfonic acid / acetone / 0 - 20 °C

6.2: 0.5 h / 20 °C

7.1: dipyridinium dichromate / N,N-dimethyl-formamide / 20 h / 20 °C

8.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / dichloromethane / 12 h / 20 °C

9.1: hydrogenchloride; water / tetrahydrofuran / 12 h / 20 °C

With hydrogenchloride; dipyridinium dichromate; dicobalt octacarbonyl; di-isopropyl azodicarboxylate; tetrabutyl ammonium fluoride; water; sodium methylate; benzotriazol-1-ol; toluene-4-sulfonic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; N-ethyl-N,N-diisopropylamine; triphenylphosphine; In tetrahydrofuran; methanol; ethanol; dichloromethane; N,N-dimethyl-formamide; acetone; 3.1: Mitsunobu reaction / 3.2: Mitsunobu reaction;
DOI:10.5012/bkcs.2011.32.5.1620