Home Cart Sign in  
Chemical Structure| 1092390-01-6 Chemical Structure| 1092390-01-6

Structure of 1092390-01-6

Chemical Structure| 1092390-01-6

*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 [ 1092390-01-6 ]

CAS No. :1092390-01-6
Formula : C30H19Br
M.W : 459.38
SMILES Code : BrC1=C2C=CC=CC2=C(C3=CC=C(C4=C5C=CC=CC5=CC=C4)C=C3)C6=CC=CC=C16
MDL No. :MFCD20486477

Safety of [ 1092390-01-6 ]

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 [ 1092390-01-6 ]

* 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 [ 1092390-01-6 ]

[ 1092390-01-6 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 870774-25-7 ]
  • [ 523-27-3 ]
  • [ 1092390-01-6 ]
YieldReaction ConditionsOperation in experiment
97.5% With tetrakis(triphenylphosphine) palladium(0); sodium carbonate; In ethanol; water; toluene; for 1.5h;Inert atmosphere; Reflux; In a 1000ml three-necked flask, with mechanical stirring, Ar gas protection, 11.7g of 9,10-dibromoanthracene (molecular weight(0.35, 0.035 mol), 8.7 g of 4- (1-naphthyl) benzeneboronic acid (molecular weight: 248,0.035 mol), and Pd (PPh3)1.8 g (molecular weight 1154, 0.001556 mol), 120 ml (2M) of sodium carbonate aqueous solution, 250 ml of toluene and 150 ml of ethanol. The mixture was stirred and refluxed, and the reaction was monitored by TLC. The reaction was complete after 1.5 hrs of reaction. Cooled, separated, evaporated to dryness, the product was isolated by column chromatography, drenchedLotion with 1: 5 ethyl acetate: petroleum ether gave 15.8 g of a white solid9- (4- (1-naphthyl) phenyl) -10-bromoanthracene (AN1), product molecular weight 458, purity 98.7%, yield: 97.5%.
9,10-Dibromoanthracene (10 g, 0.03 mol), tetrakis(triphenylphosphine)palladium(0) (1.72 g, 1.49 mmol) and <strong>[870774-25-7]4-(naphthalene-1-yl)phenylboronic acid</strong> (7.4 g, 0.03 mol) were dissolved in THF (350 mL) in a double-necked flask and stirred for 30 min. Then, potassium carbonate (2 M, 200 mL) was added dropwise over 20 min. The mixture was degassed and refluxed overnight at 80 C under a nitrogen atmosphere. After being cooled, the solvent was evaporated under vacuum, and the product was extracted with ethyl acetate and water. The ethyl acetate solution was washed with water and dried with MgSO4. Evaporation of the solvent, followed by column chromatography using n-hexane on a silica gel, yielded a white yellow product
  • 2
  • [ 870774-25-7 ]
  • [ 1564-64-3 ]
  • [ 1092390-01-6 ]
  • 3
  • 1-(4-iodophenyl)naphthalene [ No CAS ]
  • [ 641144-16-3 ]
  • [ 1092390-01-6 ]
YieldReaction ConditionsOperation in experiment
85.4% With tetrakis(triphenylphosphine) palladium(0); potassium carbonate; In ethanol; water; toluene;Inert atmosphere; Reflux; (1) In a 250 mL three-necked flask, purge nitrogen and add 0.02 mol b-1.0.022mol a-1 and 0.06molK2CO3, add 150mlToluene,Acetic acidMixed solution with water,Then add 0.0003mol of tetrakis (triphenylphosphine) palladium and stir,heatingReflux reaction10 hours,Sampling the plate, the reaction is complete. Natural cooling,It was extracted with 200 ml of ethyl acetate, the layers were separated, the extract was dried over anhydrous sulfuric acid, filtered,The filtrate was rotary evaporated and purified through a silica gel column to obtain intermediate I.The yield was 85.4%.
 

Historical Records

Categories