Home Cart Sign in  
Chemical Structure| 123792-64-3 Chemical Structure| 123792-64-3

Structure of 123792-64-3

Chemical Structure| 123792-64-3

*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 [ 123792-64-3 ]

CAS No. :123792-64-3
Formula : C9H11N3O2
M.W : 193.20
SMILES Code : O=[N+](C1=CC2=C(N=C1)CCN(C)C2)[O-]

Safety of [ 123792-64-3 ]

Application In Synthesis of [ 123792-64-3 ]

* 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 [ 123792-64-3 ]

[ 123792-64-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1445-73-4 ]
  • [ 14150-94-8 ]
  • [ 123792-64-3 ]
YieldReaction ConditionsOperation in experiment
48% With ammonia; In methanol; at 50℃;Schlenk technique; In a schlenk reactor, a solution of <strong>[14150-94-8]1-methyl-3,5-dinitro-1H-pyridin-2-one</strong> (5.00 g, 25.11mmol) and 1-methyl-4-piperidone (3.13 g, 27.62 mmol) in ammonia (7N in MeOH) (43mL) was stirred overnight at 50 C. After cooling down to rt, the mixture was evaporatedin vacuo, taken-up in DCM and a saturated aqueous solution of NaHCO3 was added. Thelayers were separated and the aqueous layer was extracted with DCM (three times). The combined organic layers were dried over MgSO4, filtered off and evaporated in vacuo togive 2.32 g of intermediate 128 (48% yield, reddish solid) which was used in the next step without further purification.
 

Historical Records

Categories