Home Cart Sign in  
Chemical Structure| 1201649-79-7 Chemical Structure| 1201649-79-7

Structure of 1201649-79-7

Chemical Structure| 1201649-79-7

*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 [ 1201649-79-7 ]

CAS No. :1201649-79-7
Formula : C54H37N
M.W : 699.88
SMILES Code : N1(C2=CC=CC=C2)C3=C(C4=C1C=CC(C5=CC(C6=CC=CC=C6)=CC(C7=CC=CC=C7)=C5)=C4)C=C(C8=CC(C9=CC=CC=C9)=CC(C%10=CC=CC=C%10)=C8)C=C3
MDL No. :MFCD19441372

Safety of [ 1201649-79-7 ]

Application In Synthesis of [ 1201649-79-7 ]

* 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 [ 1201649-79-7 ]

[ 1201649-79-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1036378-83-2 ]
  • [ 57103-20-5 ]
  • [ 1201649-79-7 ]
YieldReaction ConditionsOperation in experiment
60% With tetrakis(triphenylphosphine) palladium(0); potassium carbonate; In ethanol; toluene; for 20h;Reflux; Inert atmosphere; 1.20 g (3.0 mmol) of <strong>[57103-20-5]3,6-dibromo-9-phenylcarbazole</strong>, 2.35 g (6.6 mmol) of TPDOB, 8.0 ml of 2 M potassium carbonate aqueous solution, 60 ml of toluene and 30 ml of ethanol and nitrogen bubbling was carried out for 1 hour .40.21 g (0.18 mmol) of Pd (PPh 3) was added and refluxed for 4 hours.The organic layer was extracted with toluene and washed with saturated brine.The organic layer was dried over anhydrous magnesium sulfate, filtered, concentrated and purified by silica gel column chromatography (developing solvent: hexane / toluene = 5/1 => 3/1) to obtain a white solid.Confirmation of the target substance was carried out by 1 H-NMR, MS. (Yield 1.27 g, yield 60percent)
 

Historical Records