Home Cart Sign in  
Chemical Structure| 98792-02-0 Chemical Structure| 98792-02-0

Structure of 98792-02-0

Chemical Structure| 98792-02-0

*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 [ 98792-02-0 ]

CAS No. :98792-02-0
Formula : C10H6ClN3
M.W : 203.63
SMILES Code : ClC1=NC=NC2=C1NC3=C2C=CC=C3
MDL No. :MFCD00457089

Safety of [ 98792-02-0 ]

Application In Synthesis of [ 98792-02-0 ]

* 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 [ 98792-02-0 ]

[ 98792-02-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 849217-60-3 ]
  • [ 98792-02-0 ]
  • N-(4-((5H-pyrimido[5,4-b]indol-4-yl)oxy)phenyl)-N'-(4-fluorophenyl)cyclopropane-1,1-diamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
75.1% With potassium carbonate; In N,N-dimethyl-formamide; at 80℃; for 24h;Inert atmosphere; 4-chloro-5H-pyrimido[5,4-b]indole (M-1) (1.22g, 6mmol) and <strong>[849217-60-3]N'-(4-fluorophenyl)-N-(4-hydroxyphenyl)cyclopropane-1,1-diamide</strong> (1.57g, 5mmol) (M-1') dissolved in DMF 35mL was added K2CO3 (2.07g, 15mmol). The reaction mixture was placed under nitrogen. The reaction was stirred at 80C for 24h. After completion of the reaction, ethyl acetate 100mL was added and diluted. It was washed successively with 100mL water and 100mL saturated brine. The organic layer was dried over anhydrous sodium sulfate and filtered. Concentrated under reduced pressure. The residue was treated with ethyl acetate and petroleum ether (V / V, 10: 1) and beating washed to obtain a white 2.17g desired product I-1, yield: 75.1%.
 

Historical Records

Technical Information

Categories