8-oxoG-clamp

Base Information

Chemical Name:8-oxoG-clamp
CAS No.:223792-87-8
Molecular Formula:C₂₅H₂₆N₄O₈
Molecular Weight:510.503
Hs Code.:

Synonyms:8-oxoG-clamp

Suppliers and Price of 8-oxoG-clamp

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
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price

Total 1 raw suppliers

Chemical Property of 8-oxoG-clamp

Chemical Property:

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 8-oxoG-clamp

There total 4 articles about 8-oxoG-clamp 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: 95.0%

: C₂₉H₃₁BrN₄O₁₀

: 223792-87-8
8-oxoG-clamp

Guidance literature:: With ammonia; In methanol; for 72h;
DOI:10.1021/ol701826x

Reference yield:

: 77987-49-6
benzyl 2-hydroxyethylcarbamate

: C₂₁H₂₄BrN₃O₈

: 223792-87-8
8-oxoG-clamp

Guidance literature:: benzyl 2-hydroxyethylcarbamate; C₂₁H₂₄BrN₃O₈; With triphenylphosphine; diethylazodicarboxylate; In dichloromethane; at 20 ℃;

With N-ethyl-N,N-diisopropylamine; In ethanol; Reflux;

With ammonium hydroxide; In ethanol; at 20 ℃;
DOI:10.1016/j.antiviral.2019.01.010

Reference yield:

: 3163-15-3
2-aminoresorcinol

: 223792-87-8
8-oxoG-clamp

Guidance literature:: Multi-step reaction with 2 steps

1.1: triphenylphosphine / tetrachloromethane; dichloromethane / Reflux

1.2: 20 °C

2.1: triphenylphosphine; diethylazodicarboxylate / dichloromethane / 20 °C

2.2: Reflux

2.3: 20 °C

With triphenylphosphine; diethylazodicarboxylate; In tetrachloromethane; dichloromethane;
DOI:10.1016/j.antiviral.2019.01.010