Home Cart Sign in  
Chemical Structure| 1067192-49-7 Chemical Structure| 1067192-49-7

Structure of 1067192-49-7

Chemical Structure| 1067192-49-7

*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 [ 1067192-49-7 ]

CAS No. :1067192-49-7
Formula : C11H14N2O
M.W : 190.24
SMILES Code : CC(C)(C1=CC=C(N)C(OC)=C1)C#N

Safety of [ 1067192-49-7 ]

Application In Synthesis of [ 1067192-49-7 ]

* 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 [ 1067192-49-7 ]

[ 1067192-49-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1067192-49-7 ]
  • [ 1197953-49-3 ]
  • C23H25ClN5O2P [ No CAS ]
YieldReaction ConditionsOperation in experiment
32.4% With hydrogenchloride; In 2-methoxy-ethanol; isopropyl alcohol; at 120℃;Inert atmosphere; Add compound 25 (1.5 g, 7.9 mmol) to a 50 mL single-mouth bottle equipped with a magnetic stirrer and a condenser.Compound 7 (2.5 g, 7.9 mmol)And ethylene glycol monomethyl ether (15mL),Stir and dissolve,Adding hydrogen chloride in isopropanol solution(11.8mmol, 2.4mL, 5M)The temperature was raised to 120 C under a nitrogen atmosphere and stirred to react overnight. Cool to room temperature,Add water (30 mL) and saturated sodium bicarbonate (30 mL).Extracted with dichloromethane (40 mL x 3),Combine the organic phase,Washed with saturated saline,Dry with anhydrous sodium sulfate, filter, concentrate,The residue was passed through a silica gel column to give a white solid.The yield was 32.4%.
 

Historical Records