Home Cart Sign in  
Chemical Structure| 94956-98-6 Chemical Structure| 94956-98-6

Structure of 94956-98-6

Chemical Structure| 94956-98-6

*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 [ 94956-98-6 ]

CAS No. :94956-98-6
Formula : C11H12O2
M.W : 176.21
SMILES Code : O=CC1=CC=CC(OC)=C1CC=C
MDL No. :N/A

Safety of [ 94956-98-6 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H312-H332
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P330-P363-P501

Application In Synthesis of [ 94956-98-6 ]

* 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 [ 94956-98-6 ]

[ 94956-98-6 ] Synthesis Path-Downstream   1~5

  • 3
  • [ 40359-32-8 ]
  • [ 74-88-4 ]
  • [ 1378359-97-7 ]
  • [ 94956-98-6 ]
  • 4
  • [ 74-83-9 ]
  • [ 79950-42-8 ]
  • [ 94956-98-6 ]
  • 5
  • [ 79950-42-8 ]
  • [ 77-78-1 ]
  • [ 94956-98-6 ]
YieldReaction ConditionsOperation in experiment
90.8% With potassium carbonate; In acetonitrile; at 20 - 45℃; Compound (3) (150 g) was added to the mixture of acetonitrile (750 ml) and potassium carbonate (192 g). The resultant mixture was stirred at 20 to 30 C followed by gradual addition of dimethyl sulfate (128 g) at the same temperature. The reaction mass was stirred at 20 to 45C, till completion, as monitored by HPLC. (0118) After completion, the reaction mixture was concentrated, and water (750 ml) was added to it. The resultant mass was stirred at 50 to 60 C, cooled and MTBE was added to it. The organic layer was separated and aqueous sodium hydroxide solution (14.8 g NaOH in 149 ml water was added to it with continuous stirring. Separation and concentration of the organic layer gave Compound (4beta). Yield: 148 g (90.8%).
 

Historical Records