Home Cart Sign in  
Chemical Structure| 89532-94-5 Chemical Structure| 89532-94-5

Structure of 89532-94-5

Chemical Structure| 89532-94-5

*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 [ 89532-94-5 ]

CAS No. :89532-94-5
Formula : C6H8N2O3
M.W : 156.14
SMILES Code : O=C(C(CC1)=NNC1=O)OC
MDL No. :MFCD09959863

Safety of [ 89532-94-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 89532-94-5 ]

* 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.

  • Upstream synthesis route of [ 89532-94-5 ]

[ 89532-94-5 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 89532-94-5 ]
  • [ 63001-30-9 ]
YieldReaction ConditionsOperation in experiment
58% With pyridine; manganese(IV) oxide In toluene at 65℃; Manganese dioxide (3.12 g, 35.9 mmol) was suspended as a slurry in toluene (10 mL) and pyridine (720 μL). A sample of S47 (280 mg, 1.8 mmol) was added portionwise to the stirring solution and the resulting mixture was warmed at 65 °C until the disappearance of all starting material (6 h). The warm solution was filtered through a pad of Celite that was washed with several hundred milliliters of hot EtOAc and THF. The organic wash was evaporated to afford a yellowish solid which was used without further purification (160 mg, 58percent): 1H NMR (CDCl3, 300 MHz) δ 7.92 (d, IH, J = 9.9 Hz), 7.02 (d, IH, J = 9.8 Hz), 3.99 (s, 3H); HRMS-ESI-TOF m/z 155.0450 ([M+H+, C6H6N2O3 requires 155.0451).
References: [1] Journal of Medicinal Chemistry, 2008, vol. 51, # 15, p. 4392 - 4403.
[2] Patent: WO2010/5572, 2010, A2, . Location in patent: Page/Page column 85.
 

Historical Records

Technical Information

Categories