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8-Bromoxanthosine

Base Information Edit
  • Chemical Name:8-Bromoxanthosine
  • CAS No.:3001-46-5
  • Molecular Formula:C10H11 Br N4 O6
  • Molecular Weight:363.125
  • Hs Code.:2934999090
  • European Community (EC) Number:221-081-0
  • Nikkaji Number:J205.289J
  • Wikidata:Q76009710
  • Mol file:3001-46-5.mol
8-Bromoxanthosine

Synonyms:8-Bromoxanthosine;3001-46-5;EINECS 221-081-0;8-Bromo-9-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-9H-purine-2,6-diol;C10H11BrN4O6;C10-H11-Br-N4-O6;Xanthosine, 8-bromo-;SCHEMBL2887990;NSC 79215;8-bromo-9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-9H-purine-2,6-diol

Suppliers and Price of 8-Bromoxanthosine
Supply Marketing:Edit
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 17 raw suppliers
Chemical Property of 8-Bromoxanthosine Edit
Chemical Property:
  • Boiling Point:°Cat760mmHg 
  • Flash Point:°C 
  • PSA:153.98000 
  • Density:2.62g/cm3 
  • LogP:-1.38850 
  • XLogP3:-1.4
  • Hydrogen Bond Donor Count:5
  • Hydrogen Bond Acceptor Count:7
  • Rotatable Bond Count:2
  • Exact Mass:361.98620
  • Heavy Atom Count:21
  • Complexity:467
Purity/Quality:

99%, *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C(C1C(C(C(O1)N2C3=C(C(=O)NC(=O)N3)N=C2Br)O)O)O
  • Isomeric SMILES:C([C@@H]1[C@H]([C@H]([C@@H](O1)N2C3=C(C(=O)NC(=O)N3)N=C2Br)O)O)O
  • Use Description 8-Bromoxanthosine, a specific chemical compound, serves distinct roles in various fields. In the pharmaceutical sector, it plays a crucial role as a potential precursor or intermediate in the synthesis of pharmaceutical compounds, contributing to drug discovery and the development of molecules with potential therapeutic applications. In organic chemistry, this compound acts as a building block, enabling the creation of complex molecular structures for research purposes. Additionally, in the field of biochemical research, it may be utilized to study nucleoside metabolism and related cellular processes. Its applications in pharmaceuticals, organic synthesis, and biochemical research underscore its significance in driving innovation, scientific exploration, and potential medical breakthroughs across these different fields.
Technology Process of 8-Bromoxanthosine

There total 2 articles about 8-Bromoxanthosine 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:

Guidance literature:
8-Brom-guanosin, Eg., wss. NaNO2, 5 h;
DOI:10.1021/ja01060a057

Reference yield:

Guidance literature:
Xanthosin-dihydrat, Methylcellosolve, wfr. CaCO3, Br2/wfr. Dioxan, 40-50grad;
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