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C12H15BrN4O4

Base Information
  • Chemical Name:C12H15BrN4O4
  • CAS No.:1637533-84-6
  • Molecular Formula:C12H15BrN4O4
  • Molecular Weight:359.179
  • Hs Code.:
C<sub>12</sub>H<sub>15</sub>BrN<sub>4</sub>O<sub>4</sub>

Synonyms:

Suppliers and Price of C12H15BrN4O4
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
  • Crysdot
  • tert-Butyl2-(8-bromo-7-methyl-2,6-dioxo-2,3,6,7-tetrahydro-1H-purin-1-yl)acetate 97%
  • 100mg
  • $ 383.00
  • Chemenu
  • tert-Butyl2-(8-bromo-7-methyl-2,6-dioxo-2,3,6,7-tetrahydro-1H-purin-1-yl)acetate 95+%
  • 1g
  • $ 2079.00
  • Chemenu
  • tert-Butyl2-(8-bromo-7-methyl-2,6-dioxo-2,3,6,7-tetrahydro-1H-purin-1-yl)acetate 95+%
  • 250mg
  • $ 693.00
  • Chemenu
  • tert-Butyl2-(8-bromo-7-methyl-2,6-dioxo-2,3,6,7-tetrahydro-1H-purin-1-yl)acetate 95+%
  • 100mg
  • $ 341.00
Total 6 raw suppliers
Chemical Property of C12H15BrN4O4
Chemical Property:
Purity/Quality:

99%, *data from raw suppliers

tert-Butyl2-(8-bromo-7-methyl-2,6-dioxo-2,3,6,7-tetrahydro-1H-purin-1-yl)acetate 97% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of C12H15BrN4O4

There total 6 articles about C12H15BrN4O4 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:
Guidance literature:
With potassium tert-butylate; In 1,4-dioxane; at 20 ℃; for 1h;
Guidance literature:
Multi-step reaction with 6 steps
1: acetic acid / 10 h / 110 °C
2: N-Bromosuccinimide / dichloromethane / 20 h / 20 °C
3: hydrazine hydrate / ethanol / 2 h / 80 °C
4: triethylamine / dichloromethane / 1 h / 0 °C / Inert atmosphere
5: dichloromethane / 1 h / 0 °C
6: potassium tert-butylate / 1,4-dioxane / 1 h / 20 °C
With N-Bromosuccinimide; potassium tert-butylate; hydrazine hydrate; acetic acid; triethylamine; In 1,4-dioxane; ethanol; dichloromethane;
Guidance literature:
Multi-step reaction with 5 steps
1: N-Bromosuccinimide / dichloromethane / 20 h / 20 °C
2: hydrazine hydrate / ethanol / 2 h / 80 °C
3: triethylamine / dichloromethane / 1 h / 0 °C / Inert atmosphere
4: dichloromethane / 1 h / 0 °C
5: potassium tert-butylate / 1,4-dioxane / 1 h / 20 °C
With N-Bromosuccinimide; potassium tert-butylate; hydrazine hydrate; triethylamine; In 1,4-dioxane; ethanol; dichloromethane;
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