Home Cart Sign in  
Chemical Structure| 72119-43-8 Chemical Structure| 72119-43-8

Structure of 72119-43-8

Chemical Structure| 72119-43-8

*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 [ 72119-43-8 ]

CAS No. :72119-43-8
Formula : C12H18N2
M.W : 190.28
SMILES Code : CCN1CCN(CC)C2=C1C=CC=C2

Safety of [ 72119-43-8 ]

Application In Synthesis of [ 72119-43-8 ]

* 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 [ 72119-43-8 ]

[ 72119-43-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 72119-43-8 ]
  • [ 1450-93-7 ]
  • (E)-6-((1H-imidazol-2-yl)diazenyl)-1,4-diethyl-1,2,3,4-tetrahydroquinoxaline [ No CAS ]
YieldReaction ConditionsOperation in experiment
2-Aminoimidazole sulfate (11.6 g) is dissolved in 7.4 mL of concentrated HCl, 8 mL of water, and 40 mL of acetic acid. The resulting solution is cooled to 0° C. To the solution is added a solution of 6.08 g of NaNO2 in 16 mL of water dropwise where the internal temperature is maintained under 5° C. The resulting yellow-brown solution is stirred for 30 minutes at 0° C. In a separate flask equipped with a mechanical stirrer a mixture of 1,4-diethyl-1,2,3,4-tetrahydroquinoxaline, 13.1 g of sodium acetate and 40 mL of acetic acid is cooled to 0° C. To this slurry is added the diazonium solution slowly and the internal temperature of the reaction is maintained below 5° C. After the addition is complete, the resulting violet suspension is stirred for 1 hour at 0° C. The dark reaction mixture is poured into a large beaker containing 400 g ice. Aqueous NaOH (20percent) is added to the suspension slowly until pH 6.5 is reached. The mixture is extracted with dichloromethane 6 times to yield crude (E)-6-((1H-imidazol-2-yl)diazenyl)-1,4-diethyl-1,2,3,4-tetrahydroquinoxaline (19.5 g, impure). This material is used in the next step without further purification.
2-Aminoimidazole sulfate (11.6 g) is dissolved in 7.4 mL of concentrated HC1, 8 mL of water, and 40 mL of acetic acid. The resulting solution is cooled to 0 oC. To the solution is added a solution of 6.08 g of NaN02 in 16 mL of water dropwise where the internal temperature is maintained under 5 oC. The resulting yellow-brown solution is stirred for 30 minutes at 0°C. In a separate flask equipped with a mechanical stirrer a mixture of 1,4-diethyl- 1,2,3,4- tetrahydroquinoxaline, 13.1 g of sodium acetate and 40 mL of acetic acid is cooled to 0 °C. To this slurry is added the diazonium solution slowly and the internal temperature of the reaction is maintained below 5 °C. After the addition is complete, the resulting violet suspension is stirred for 1 hour at 0 °C. The dark reaction mixture is poured into a large beaker containing 400 g ice. Aqueous NaOH (20percent) is added to the suspension slowly until pH 6.5 is reached. The mixture is extracted with dichloromethane 6 times to yield crude (E)-6-((lH- imidazol-2-yl)diazenyl)- 1,4-diethyl- 1,2,3,4-tetrahy droquinoxaline (19.5g, impure). This material is used in the next step without further purification.
 

Historical Records