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8-Bromo-3-methyl-7-propan-2-ylpurine-2,6-dione

Base Information
  • Chemical Name:8-Bromo-3-methyl-7-propan-2-ylpurine-2,6-dione
  • CAS No.:123980-53-0
  • Molecular Formula:C9H11BrN4O2
  • Molecular Weight:287.11
  • Hs Code.:
  • Mol file:123980-53-0.mol
8-Bromo-3-methyl-7-propan-2-ylpurine-2,6-dione

Synonyms:123980-53-0;8-bromo-3-methyl-7-propan-2-ylpurine-2,6-dione;8-Bromo-3,7-dihydro-3-methyl-7-(1-methylethyl)-1H-purine-2,6-dione;8-bromo-7-isopropyl-3-methyl-1H-purine-2,6(3H,7H)-dione;8-bromo-3-methyl-7-(propan-2-yl)-2,3,6,7-tetrahydro-1H-purine-2,6-dione;Oprea1_571106;Oprea1_647698;IZJNENRMUGDVII-UHFFFAOYSA-N;AKOS000576801;NCGC00310160-01;Xanthine,1-methyl-7-isopropyl-8-bromo-;CS-0329215;AB01303761-01;F0373-0004;8-Bromo-7-isopropyl-3-methyl-3,7-dihydro-1H-purine-2,6-dione;8-Bromo-7-isopropyl-3-methyl-3,7-dihydro-1H-purine-2,6-dione #

Suppliers and Price of 8-Bromo-3-methyl-7-propan-2-ylpurine-2,6-dione
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
  • TRC
  • 8-Bromo-3,7-dihydro-3-methyl-7-(1-methylethyl)-1H-purine-2,6-dione
  • 500mg
  • $ 1320.00
Total 2 raw suppliers
Chemical Property of 8-Bromo-3-methyl-7-propan-2-ylpurine-2,6-dione
Chemical Property:
  • XLogP3:1.1
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:1
  • Exact Mass:286.00654
  • Heavy Atom Count:16
  • Complexity:336
Purity/Quality:

99% *data from raw suppliers

8-Bromo-3,7-dihydro-3-methyl-7-(1-methylethyl)-1H-purine-2,6-dione *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CC(C)N1C2=C(N=C1Br)N(C(=O)NC2=O)C
  • Uses 8-Bromo-3,7-dihydro-3-methyl-7-(1-methylethyl)-1H-purine-2,6-dione, is a substituted derivative of of Xanthine (X499950), found in animal organs, yeast, potatoes, coffee beans, tea. This drug can be used to relax and widen certain breathing passages of the lungs. It is also found that a large number of derivatives have adenoside receptor antagonist properties.
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