Home Cart Sign in  
Chemical Structure| 1430057-84-3 Chemical Structure| 1430057-84-3

Structure of 1430057-84-3

Chemical Structure| 1430057-84-3

*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 [ 1430057-84-3 ]

CAS No. :1430057-84-3
Formula : C6H10N2O
M.W : 126.16
SMILES Code : CN1N=CC(COC)=C1
MDL No. :MFCD28142354

Safety of [ 1430057-84-3 ]

Application In Synthesis of [ 1430057-84-3 ]

* 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 [ 1430057-84-3 ]

[ 1430057-84-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 112029-98-8 ]
  • [ 74-88-4 ]
  • [ 1430057-84-3 ]
YieldReaction ConditionsOperation in experiment
77.2% Step B 4-(methoxymethyl)-1-methyl-1,1-pyrazole To a suspension of sodium hydride (0.128 g, 3.21 mmol) in tetrahydrofuran (5 mL, 60 mmol) at 0° C. was added <strong>[112029-98-8](1-methyl-1H-pyrazol-4-yl)methanol</strong> (0.300 g, 2.68 mmol) in tetrahydrofuran (2 mL, 20 mmol). The reaction was stirred at room temperature for 1 h, and then cooled down with ice bath. Methyl iodide (0.83 mL, 13 mmol) was added. The reaction was stirred at room temperature overnight. The reaction mixture was quenched with brine and extracted with EtOAc (3*). The combined organic phases were washed with water, brine, then dried over Na2SO4, and concentrated under reduced pressure to give 261 mg (77.2percent yield) of the desired product as colorless oil, which was directly used for the next reaction. LC/MS found: 127.2 (M+1)+.
 

Historical Records