Home Cart Sign in  
Chemical Structure| 935-50-2 Chemical Structure| 935-50-2

Structure of 935-50-2

Chemical Structure| 935-50-2

*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 [ 935-50-2 ]

CAS No. :935-50-2
Formula : C8H10O3
M.W : 154.16
SMILES Code : O=C1C=CC(OC)(OC)C=C1
MDL No. :MFCD00009966

Safety of [ 935-50-2 ]

Application In Synthesis of [ 935-50-2 ]

* 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 [ 935-50-2 ]

[ 935-50-2 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 935-50-2 ]
  • [ 126717-59-7 ]
  • [ 150-76-5 ]
  • 4,4-Dimethoxy-5-(6-methoxy-2-methyl-pyridin-3-yl)-cyclohex-2-enone [ No CAS ]
  • 2
  • [ 67-56-1 ]
  • [ 13794-15-5 ]
  • [ 935-50-2 ]
  • [ 150-76-5 ]
  • [ 106-51-4 ]
  • 4
  • [ 935-50-2 ]
  • [ 15754-51-5 ]
  • (2-hydroxy-5-methoxyphenyl)bis(4-methoxyphenyl)phosphorus oxide [ No CAS ]
YieldReaction ConditionsOperation in experiment
78% With water; In toluene; at 100℃; for 12h;Schlenk technique; Inert atmosphere; 131 mg (0.5 mmol) of <strong>[15754-51-5]bis(4-methoxyphenyl)phosphine oxide</strong>, 115.5 mg (0.75 mmol) of 4,4-dimethoxy-2,5-cyclohexadien-1-one, 0.05 mmol of water and 1.0 mL of toluene were placed in a Schlenk tube under nitrogen, and the reaction was stirred at 100 C for 12 hours. After completion of the reaction, it was purified by column chromatography, and the isolated yield was 78%.
78% With water; In toluene; at 100℃; for 12h;Inert atmosphere; Green chemistry; General procedure: A mixture of quinone monoketal (0.6 mmol), H-phosphine oxide(0.5 mmol), and catalyst (20 mol% of H2O for allylic substitution,20 mol% of Et3N for 1,6-substitution) was dissolved in toluene underN2 atmosphere, stirred at 100 C or 80 C for 12 h. Uponcompletion of the reaction, the mixture was concentrated undervacuum. Removal of the solvent under a reduced pressure gave thecrude product; pure product was obtained by passing the crudeproduct through a short silica gel column using Hexane/EtOAc(2:1-5:1) as eluent.
  • 5
  • [ 935-50-2 ]
  • [ 30309-80-9 ]
  • (2-hydroxy-5-methoxyphenyl)di-o-tolylphosphine oxide [ No CAS ]
 

Historical Records