Home Cart Sign in  
Chemical Structure| 194784-10-6 Chemical Structure| 194784-10-6

Structure of 194784-10-6

Chemical Structure| 194784-10-6

*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 [ 194784-10-6 ]

CAS No. :194784-10-6
Formula : C10H10N2O4
M.W : 222.20
SMILES Code : CC(=O)NC1=C(C=CC=C1[N+]([O-])=O)C(C)=O
MDL No. :MFCD00033969

Safety of [ 194784-10-6 ]

Application In Synthesis of [ 194784-10-6 ]

* 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 [ 194784-10-6 ]

[ 194784-10-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 41018-86-4 ]
  • [ 194784-10-6 ]
  • 2
  • [ 5234-26-4 ]
  • [ 194784-10-6 ]
YieldReaction ConditionsOperation in experiment
With sulfuric acid; nitric acid; at -20 - 0℃; Step 2: N-(2-Acetyl-6-nitro-phenyl)-acetamide; A solution of N-(2-acetyl-phenyl)-acetamide (1 g, 5.65 mmol) in cone. H2SO4 (2.8 ml_, 45.2 mmol) was cooled to -200C and fuming nitric acid (2 ml_, 33 mmol) was slowly added. The reaction mixture was warmed to 00C and stirred for 7 h. After completion of the starting material, the reaction mixture was quenched with water and extracted with dichloromethane (2X25 ml_). The combined organic layers were washed with brine and water, then dried over anhydrous sodium sulphate and concontrated to dryness. The resulting residue was purified by column chromatography using 1 %methanol in chloroform to get the title compound as yellow solid
 

Historical Records

Technical Information

Categories