Home Cart Sign in  
Chemical Structure| 105902-32-7 Chemical Structure| 105902-32-7

Structure of 105902-32-7

Chemical Structure| 105902-32-7

*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 [ 105902-32-7 ]

CAS No. :105902-32-7
Formula : C13H12O
M.W : 184.23
SMILES Code : OC1=CC(C2=CC=CC=C2)=CC=C1C
MDL No. :MFCD03265274

Safety of [ 105902-32-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302+H312+H332-H315-H319
Precautionary Statements:P501-P261-P270-P271-P264-P280-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330-P302+P352+P312-P304+P340+P312

Application In Synthesis of [ 105902-32-7 ]

* 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 [ 105902-32-7 ]

[ 105902-32-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 36138-76-8 ]
  • [ 98-80-6 ]
  • [ 105902-32-7 ]
YieldReaction ConditionsOperation in experiment
General procedure: A mixture of 7, (4.6 mmol), phenyl boronic acid (5.09 mmol), and Ba(OH)2·8H2O (9.2 mmol) in 15 mL of DME:H2O (5:1) was stirred under Ar for 15 min. To this, Pd(PPh3)4 (0.46 mmol) was added and the resulting solution was refluxed for overnight. The reaction was cooled and diluted with EtOAc (30 mL) and washed with NaHCO3 and brine. The resulting organic layer dried(Na2SO4) and evaporated to give a brown solid, which was purified by column chromatography using a gradient of 1:1 Hex:EtOAc yielded a white solid (90%).
 

Historical Records

Technical Information

Categories