Home Cart Sign in  
Chemical Structure| 80798-52-3 Chemical Structure| 80798-52-3

Structure of 80798-52-3

Chemical Structure| 80798-52-3

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of [ 80798-52-3 ]

CAS No. :80798-52-3
Formula : C6H10N4O2
M.W : 170.17
SMILES Code : O=C1NC(C(N)=C(N)N1CC)=O
MDL No. :MFCD12805517

Safety of [ 80798-52-3 ]

Application In Synthesis of [ 80798-52-3 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 80798-52-3 ]

[ 80798-52-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 80798-52-3 ]
  • [ 42926-52-3 ]
  • [ 321889-90-1 ]
YieldReaction ConditionsOperation in experiment
72% With sodium hydroxide; triethylamine; In N-methyl-acetamide; a) A solution of <strong>[42926-52-3]2-ethoxybenzoyl chloride</strong> (12.0 g, 65 mmol) in dimethylformamide (10 mL) was added dropwise to a stirred solution of 5,6-diamino-1-ethyl-1H-pyrimidine-2,4-dione (10.4 g, 61 mmol) and triethylamine (9.8 mL, 65 mmol) in dimethylformamide (250 mL). The resulting mixture was stirred for 20 hours at room temperature, then evaporated under reduced pressure. Aqueous sodium hydroxide solution (1N, 98 mL, 98 mmol) was added and the mixture heated under reflux for 6 hours. The resulting solution was acidified with 1N hydrochloric acid and the precipitate collected and dried by suction to give 8-(2-ethoxyphenyl)-3-ethyl-3,7-dihydropurine-2,6-dione as a beige solid (7.0 g, 72%).
 

Historical Records