Home Cart Sign in  
Chemical Structure| 187086-32-4 Chemical Structure| 187086-32-4

Structure of 187086-32-4

Chemical Structure| 187086-32-4

*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 [ 187086-32-4 ]

CAS No. :187086-32-4
Formula : C32H19Br
M.W : 483.40
SMILES Code : BrC1=CC=C2C3=C(C4=CC=CC=C4)C5=CC=CC=C5C(C6=CC=CC=C6)=C3C7=C2C1=CC=C7
MDL No. :MFCD16038664
InChI Key :MBWSEPXTVAGLJS-UHFFFAOYSA-N
Pubchem ID :10790982

Safety of [ 187086-32-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 187086-32-4 ]

* 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 [ 187086-32-4 ]

[ 187086-32-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 952514-79-3 ]
  • [ 187086-32-4 ]
  • [ 1159358-55-0 ]
YieldReaction ConditionsOperation in experiment
5.3 g With tetrakis(triphenylphosphine) palladium(0); potassium carbonate; In ethanol; water; toluene; for 16h;Reflux; (1-phenyl-1H-benzo [d] imidazol-2-yl) phenyl) -pyrrolidine (20 g) A mixture of boronic acid (15.6 g), tetrakis (triphenylphosphine) palladium (2.40 g), toluene (300 ml), ethanol (150 ml) and a 2M aqueous solution of potassium carbonate (72.4 ml) Lt; / RTI & gt; The reaction was quenched with water,The enantiomer was removed, washed with brine, dried over anhydrous sodium sulfate and the solvent was removed under reduced pressure to give 2- (4- (7,12-diphenylbenzo [k] fluoranthene-3-yl) phenyl ) -1-phenyl-1H-benzo [d] imidazole (Compound B, 5.3 g).
 

Historical Records