5-Bromo-4-nitro-1-pentofuranosyl-1h-imidazole

Base Information

Chemical Name:5-Bromo-4-nitro-1-pentofuranosyl-1h-imidazole
CAS No.:10357-25-2
Molecular Formula:C₈H₁₀BrN₃O₆
Molecular Weight:324.088
Hs Code.:
NSC Number:105818
DSSTox Substance ID:DTXSID00908476
Mol file:10357-25-2.mol

Synonyms:10357-25-2;5-bromo-4-nitro-1-pentofuranosyl-1h-imidazole;NSC105818;DTXSID00908476;ZINC04633743;NSC-105818

Suppliers and Price of 5-Bromo-4-nitro-1-pentofuranosyl-1h-imidazole

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 5 raw suppliers

Chemical Property of 5-Bromo-4-nitro-1-pentofuranosyl-1h-imidazole

Chemical Property:

Vapor Pressure:7.77E-17mmHg at 25°C
Boiling Point:631.9°Cat760mmHg
Flash Point:336°C
Density:2.37g/cm³
XLogP3:-0.4
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:2
Exact Mass:322.97530
Heavy Atom Count:18
Complexity:328

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=NC(=C(N1C2C(C(C(O2)CO)O)O)Br)[N+](=O)[O-]

Technology Process of 5-Bromo-4-nitro-1-pentofuranosyl-1h-imidazole

There total 5 articles about 5-Bromo-4-nitro-1-pentofuranosyl-1h-imidazole 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: 55.0%

: 10512-70-6
1-(2,3,5-tri-O-acetyl-β-D-erythro-pentofuranosyl)-5-bromo-4-nitroimidazole

: 10357-25-2
5-Bromo-4-nitro-1-β-D-ribofuranosylimidazole

Guidance literature:: With ammonium hydroxide; In methanol; for 1.5h; Ambient temperature;
DOI:10.1002/jhet.5570270707

Reference yield: 50.0%

: C₂₉H₂₂BrN₃O₉

: 10357-25-2
5-Bromo-4-nitro-1-β-D-ribofuranosylimidazole

Guidance literature:: With ammonia; In methanol;

Reference yield:

: 13035-61-5
1,2,3,5-tetraacetylribose

: 10357-25-2
5-Bromo-4-nitro-1-β-D-ribofuranosylimidazole

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) chlorotrimethylsilane, ammonium sulfate, 2.) stannic chloride / 1.) hexachlorotrimethyldisilazane, reflux, 16 h, 2.) dichloroethane, r.t., 18 h

2: 55 percent / ammonium hydroxide / methanol / 1.5 h / Ambient temperature

With ammonium hydroxide; ammonium sulfate; chloro-trimethyl-silane; tin(IV) chloride; In methanol;
DOI:10.1002/jhet.5570270707