Home Cart Sign in  
Chemical Structure| 886435-69-4 Chemical Structure| 886435-69-4

Structure of 886435-69-4

Chemical Structure| 886435-69-4

*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 [ 886435-69-4 ]

CAS No. :886435-69-4
Formula : C7H10N4O2
M.W : 182.18
SMILES Code : NC1=CC(N(C)C)=NC=C1[N+]([O-])=O
MDL No. :MFCD31431953

Safety of [ 886435-69-4 ]

Application In Synthesis of [ 886435-69-4 ]

* 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 [ 886435-69-4 ]

[ 886435-69-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 2604-39-9 ]
  • [ 506-59-2 ]
  • [ 886435-69-4 ]
YieldReaction ConditionsOperation in experiment
100% Compound 8; In a microwave tube, a solution of <strong>[2604-39-9]4-amino-2-chloro-5-nitropyridine</strong> (prepared, as described for compound 9) (200 mg; 1.16 mmol) in ethanol (2 ml) was treated sequentially with dimethylamine hydrochloride (471 mg; 5.78 mmol) and triethylamine (781 mu\\; 6.96 mmol). The tube was quickly sealed and irradiated in the microwave (CEM Discover, 150 W, 85 0C, 10 min). The ethanol was evaporated, dichloromethane (15 ml) was added to dissolve the products, and the solution washed with IM sodium hydroxide solution (2 x 10 ml). The organic layer was dried (sodium sulphate), the mixture filtered and the filtrate evaporated to dryness to afford N2,N2-dimethyl-5-nitro-pyridine-2,4-diamine (240 mg, 114percent).
 

Historical Records